Loss of angiotensin II receptor expression in dopamine neurons in Parkinson’s disease correlates with pathological progression and is accompanied by increases in Nox4- and 8-OH guanosine-related nucleic acid oxidation and caspase-3 activation
© Zawada et al.; licensee BioMed Central. 2015
Received: 2 December 2014
Accepted: 20 January 2015
Published: 3 February 2015
In rodent models of Parkinson’s disease (PD), dopamine neuron loss is accompanied by increased expression of angiotensin II (AngII), its type 1 receptor (AT1), and NADPH oxidase (Nox) in the nigral dopamine neurons and microglia. AT1 blockers (ARBs) stymie such oxidative damage and neuron loss. Whether changes in the AngII/AT1/Nox4 axis contribute to Parkinson neuropathogenesis is unknown. Here, we studied the distribution of AT1 and Nox4 in dopamine neurons in two nigral subregions: the less affected calbindin-rich matrix and the first-affected calbindin-poor nigrosome 1 of three patients, who were clinically asymptomatic, but had nigral dopamine cell loss and Braak stages consistent with a neuropathological diagnosis of PD (prePD). For comparison, five clinically- and neuropathologically-confirmed PD patients and seven age-matched control patients (AMC) were examined.
AT1 and Nox4 immunoreactivity was noted in dopamine neurons in both the matrix and the nigrosome 1. The total cellular levels of AT1 in surviving dopamine neurons in the matrix and nigrosome 1 declined from AMC>prePD>PD, suggesting that an AngII/AT1/Nox4 axis orders neurodegenerative progression. In this vein, the loss of dopamine neurons was paralleled by a decline in total AT1 per surviving dopamine neuron. Similarly, AT1 in the nuclei of surviving neurons in the nigral matrix declined with disease progression, i.e., AMC>prePD>PD. In contrast, in nigrosome 1, the expression of nuclear AT1 was unaffected and similar in all groups. The ratio of nuclear AT1 to total AT1 (nuclear + cytoplasmic + membrane) in dopamine neurons increased stepwise from AMC to prePD to PD. The proportional increase in nuclear AT1 in dopamine neurons in nigrosome 1 of prePD and PD patients was accompanied by elevated nuclear expression of Nox4, oxidative damage to DNA, and caspase-3-mediated cell loss.
Our observations are consistent with the idea that AngII/AT1/Nox4 axis-mediated oxidative stress gives rise to the dopamine neuron dysfunction and loss characteristic of the neuropathological and clinical manifestations of PD and suggest that the chance for a neuron to survive increases in association with lower total as well as nuclear AT1 expression. Our results support the need for further evaluation of ARBs as disease-modifying agents in PD.
KeywordsAngiotensin Dopamine neuron NADPH oxidase Nox Nigrosome Oxidative stress Parkinson’s RAS Substantia nigra
The renin-angiotensin system (RAS) in the brain is physically separated from the peripheral RAS by the blood–brain barrier (BBB) . Because it regulates blood pressure and volume, RAS in the periphery is especially important for survival in the case of hemorrhage . For this, circulating AngII binds to its type 1 receptor (AT1) on vascular smooth muscle cells  to induce vasoconstriction. The presence of a brain specific RAS and its potential as a regulator of the brain’s response to stress has been demonstrated in rodent , primate, and human brain . Coordinated synthesis of AngII and AT1 in both neurons and glia in adult rat brain coincides with localization of AT1 on endolysosomes , on mitochondria, and in nuclei . The first hint of a nuclear-delimited function of AngII came in the early 1970s, when trafficking of radiolabelled AngII into the nuclear compartment of smooth muscle cells was first reported, suggesting that nuclear AngII/AT1 signaling influences transcription . In addition, AngII binding to AT1 in the mature brain contributes to: i) the maintenance of blood pressure ; ii) calcium-dependent hypothalamic neuron depolarization ; and iii) dopamine release from dopaminergic neurons [10,11]. On the other hand, AngII binding to AT1 during brain development favors: iv) neurogenesis  and v) differentiation of dopamine neurons .
The original link between AngII/AT1 and dopaminergic neurotransmission was established in the late 1970s by Simonnet and Giorguieff-Chesselet in a report on AngII-evoked release of dopamine from rat striatal slices . Subsequently, autoradiography revealed AT1 binding sites in human nigral dopaminergic cell bodies and in the striatum in dopaminergic terminals [14,15]. These findings raised, for the first time, the possibility of the existence of a functionally active, self-contained AngII/AT1 system in dopamine neurons in substantia nigra that might be relevant to Parkinson’s disease. Indeed, studies in rodent models of Parkinson’s demonstrated that angiotensin receptor blockers (ARBs) such as losartan protect dopamine neurons from the degenerative effects of 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) in mice [4,16] and 6-hydroxydopamine (6-OHDA) in rats [17,18]. The neurodegenerative consequences of the AT1 activation might come from AT1-mediated stimulation of a multimeric NADPH oxidase (Nox) for production of excessive levels of superoxide, as we demonstrated for Nox2 in cultured rat dopaminergic cells  and for Nox4 in murine neural stem cells .
As rat dopamine neurons demonstrate an increase in the numbers of AT1 in response to 6-OHDA treatment  as well as with increased age, we posit here that elevation of expression of AT1 presages dopamine neuron dysfunction and loss. In parallel to these increases in the AT1 following intrastriatal 6-OHDA injection, p47 and Nox2, which are cytoplasmic and catalytic Nox subunits, respectively, are also elevated; thus, Nox is activated and oxidative damage to macromolecules ensues . These responses are not limited to 6-OHDA models, as we have reported that a selective dopaminergic neurotoxin, 1-methyl-4-phenylpyridinium (MPP+), elevates expression of Nox2 and promotes Nox2-dependent superoxide generation in a midbrain-derived rat dopaminergic cell line and that these pathogenic effects are reduced by losartan . These findings are consistent with a role for AngII/AT1/Nox-mediated oxidative stress in the initiation and progression of neurodegeneration in neurotoxin-induced Parkinson models. Our earlier report on the expression of p47 and Nox2 in dopaminergic neurons in the adult human substantia nigra , together with a demonstration in a human brain by Garrido-Gill and colleagues of nigral intraneuronal RAS , support the notion of a direct link between AngII/AT1 and Nox/superoxide generation in human dopamine neurons. Until now, there existed only a single report suggesting that in humans the response of the brain RAS to degenerative conditions results in a change in AT1 numbers. Although the phenotypic identity of the neural cells examined was not identified by this 1996 report by Ge and Barnes , they did report that relative to that present in age-, sex-, and post-mortem interval-matched neurologically normal individuals, there is a marked reduction in AngII binding to AT1 in the caudate, putamen, and substantia nigra in brains of Parkinson patients.
In order to identify and characterize AT1-related changes as a function of neurological and neuropathological changes characteristic of PD, we studied the distribution and levels of expression of AT1 in substantia nigra of three groups of patients: those who had neuropathological changes consistent with PD, but were asymptomatic as to motor dysfunction (pre-PD); those with frank PD; and patients of similar ages who died neurologically and neuropathologically intact (AMC). For a comparison of data from these cases, we developed a semi-quantitative immunofluorescence microscopy-based strategy for systematic analysis of the AT1 within subdivisions of the substantia nigra with regard to its steady state levels as well as its specific subcellular location in dopamine neurons in nigral tissue sections. The rationale for examining the matrix and nigrosome 1 subdivisions arose from earlier demonstrations by Damier and colleagues that human substantia nigra is compartmentalized into distinct zones termed nigrosomes 1–5 (calbindin poor) and matrix (calbindin rich)  and that the nigrosome 1 is the site of the earliest loss of dopamine neurons in Parkinson’s . Reasoning that these nigral compartments might engender differential changes to the AT1-related pathogenic pathway, we examined these distinct nigral regions and found that the whole-cell levels of AT1 in dopamine neurons were gradually reduced in both nigral matrix and nigrosome 1 in a pattern indicative of a disease-related progression (AMC>prePD>PD). In contrast to the attendant and similar losses of AT1 in dopamine neurons and their nuclei in neurons of the nigral matrix, the nuclear AT1 profile in neurons of nigrosome 1 differed distinctly, i.e., the ratio of nuclear/total neuron AT1 expression was elevated with disease progression. Disease progression was also associated with increased levels of Nox4, StressMarq-detected oxidative damage to nucleic acids, and active caspase-3 in the nuclei of dopamine neurons.
Materials and methods
Case selection and neuropathological assessment
Age, gender, clinical diagnosis, cause of death, post-mortem interval, and brain weight for control, prePD, and PD cases
All prePD and PD cases are α-synuclein Braak stage 6
Age (y)/ gender
Cause of death
Brain weight (g)
Tissue preparation, immunohistochemical detection of Calbindin D28k, and immunohistofluorescence
Antibodies used and antigen unmasking procedures employed
42, Mouse IgG1
Rat α-synuclein 15-123
70% Formic acid for 10 min
Synthetic peptide mapping @ N-terminus of human AT1
Microwave in 10 mM citrate buffer pH 6 for 30 min
Rat calbindin D28k
Microwave in 10 mM citrate buffer pH 6 for 30 min
m Mouse 15A3
8-hydroxy-guanosine-BSA and -casein conjugates
Microwave in 10 mM citrate buffer pH 6 for 30 min
Bovine full length native protein
Trypsin @37°C for 10 min
Synthetic peptide of C-terminus of Iba1 conserved between humans, rats, and mice
Microwave in 10 mM citrate buffer pH 6 for 30 min
Human nucleoporin 62 aa. 24-178
Microwave in 10 mM citrate buffer pH 6 for 30 min
BD Transduction Laboratories
Whole neuron marker
Microwave in 10 mM citrate buffer pH 6 for 30 min
Synthetic peptide within NADPH binding domain of human Nox4 (Q9NPH5)
Microwave in 10 mM citrate buffer pH 6 for 30 min
Trypsin @37°C for 10 min
Dr. Linda Van Eldik
Synthetic peptide mapping @ N-terminus of human TH
Microwave in 10 mM citrate buffer pH 6 for 30 min
Sections that were used for immunohistofluorescence were treated with 0.1% Sudan Black B (Sigma) in 70% ethanol to block lipofuscin autofluorescence. All immunoreactions were by overnight incubation at room temperature. Appropriate Alexa Fluor-tagged secondary antibodies were diluted in antibody diluent 1:200 (DAKO), and sections were incubated for 60 minutes, washed three times for 5 minutes each in distilled water, and coverslipped with prolong Gold with DAPI (Invitrogen) for DNA/nuclear staining. For each set of slides, one no primary antibody control section was treated exactly the same, including the secondary antibody. On two occasions, prior to immunohistofluorescence procedure on human SN sections, additional controls were run by pre-absorbing primary antibody against AT1 at 4°C overnight with AT1 blocking peptide (Santa Cruz Cat# sc-1173 P) against which the primary antibody was raised. The weight ratio of the primary AT1 antibody to the AT1 blocking peptide that totally prevented detection of the AT1 in SN was 1:50 (0.5 μg antibody:25 μg blocking peptide). At ratios of 1:20 and 1:10, the blocking peptide was also effective in lowering the intensity of AT1 fluorescence, but to a lesser extent than the complete AT1 signal blockade seen at the antibody to peptide ratio of 1:50 (data not shown). To confirm the staining pattern obtained with the primary anti-AT1 antibody from Santa Cruz, we have performed immunohistofluorescent staining of select sections from human brain with an alternative primary anti-AT1 antibody made in goat (Sigma Cat# SAB2500038).
Semiquantitative assessment of AT1 in nigral TH-immunoreactive dopamine neurons
The expression of AT1 in TH-immunoreactive dopamine neurons of human substantia nigra was quantified using similar methods to those that we have previously described in different cell types including S100B- and GFAP-immunoreactive astrocytes and Iba1-immunoreactive microglia [26-28]. In the current study, each of the nigral sections examined contained both the calbindin poor nigrosome 1 region as well as the calbindin rich matrix (Figure 1). In each nigral section, the nigrosome 1 and matrix regions were identified based on the level of calbindin D28k immunodetection, and within each, a single square Area Of Interest (AOI) spanning 9.0 mm2 was identified. Each AOI was further parcelated into fields of interest each equal to 37638.6 μm2 and representing the entire area of a 40× photomicrograph. Three consecutive photomicrographs, one of each fluorescence channel starting with red (TRITC for AT1), followed by green (FITC for TH), and ending with blue (DAPI for nuclei) were captured for each section at predetermined and fixed exposure settings for each fluorophore (TRITC at 500 ms; FITC at 2 s; DAPI at 200 ms) using a Nikon Eclipse E600 microscope equipped with a CoolSNAP™ EZ monochrome CCD camera (Photometrics). For each patient, all neurons immunopositive for TH were counted in one AOI within matrix and one AOI within nigrosome 1 of one section, i.e., within the same AOIs that were used for AT1 detection and intensity measurement. For a neuron to be counted it had to be TH+ and contain a DAPI-labelled nucleus. The TH+ neuron counts (density) are reported as TH+ neurons/mm2.
In order to measure the intensity of AT1 expression in dopamine neurons, all TH- immunopositive neurons (FITC fluorescence) within the nigrosome 1 AOI and within the matrix AOI in each photomicrograph had their perimeter manually outlined with an area-polygon selection tool in Nikon software NIS-Elements BR3 software (Nikon). To quantify the intensity of AT1 in each whole dopamine neuron profile, the outline of each dopamine neuron profile (FITC channel) was copied and pasted into the TRITC fluorescence channel exactly in the same location on the photomicrograph as that for the FITC channel. Similarly, the intensity of nuclear AT1 was measured by outlining the nuclei (DAPI fluorescence) of dopamine neurons and copying and pasting the resulting outline into the TRITC channel. For the AT1-related fluorescence intensity quantification used as an index of the AT1 abundance, the sum intensity in each neuron within the AOI and within each nucleus were averaged for the group of neurons in the matrix and in nigrosome 1 for comparisons of AT1 intensity per neuron and per nucleus in these two nigral regions. The number of dopamine neurons and their nuclei examined within AOIs was within the following ranges: i) in AMC cases from 41 to 154 in matrix and from 39 to 140 in nigrosome 1; ii) in prePD cases from 71 to 147 in matrix and from 21 to 47 in nigrosome 1; and iii) in PD cases from 10 to 151 in matrix and from 10 to 44 in nigrosome 1. In total, 2086 dopamine neurons were analyzed using immunofluorescence intensity measures in order to estimate AT1 expression levels in dopamine neurons and their nuclei.
Semiquantitative assessment of the degree of neuronal stress in nigral TH- and AT1-immunoreactive dopamine neurons and AT1 detection at the nuclear membrane
The numbers of nuclei in pigmented neurons that contained both Nox4/AT1 and StressMarq/AT1 immunoreactivity, or contained neither were counted in three fields captured at 40× magnification from both matrix and nigrosome 1 in each patient. The numbers of dopamine neuron nuclei examined within these three fields were as follows: i) in AMC cases 104; ii) in prePD cases 81; and iii) in PD cases 179. In total, 147 dopamine neurons were analyzed to detect the presence of nuclear Nox4 and 103 dopamine neurons were analyzed to detect the presence of nuclear StressMarq. To determine correlations between the presence of Nox4 and StressMarq in AMC, versus prePD, versus PD, the percentage of Nox4 and StressMarq immunoreactive nuclei was determined and expressed as a percentage of affected neurons. To determine if the nuclear AT1 was associated with nuclear membrane, selected tissue sections were co-immunoreacted with antibodies targeting AT1 and nucleoporin 62 (Nup62) and to assess the degree of injury associated changes in dopamine neurons, one tissue section of substantia nigra from each patient was immunoreacted with active caspase-3 antibody allowing detection of the intensity and sub-cellular localization of caspase-3 in matrix and nigrosome 1 relative to neurological and neuropathological change.
Data are expressed as mean ± SEM with significance set at p ≤ 0.05. To assess differences among groups, data were analyzed by one way ANOVA followed by Student-Newman-Keuls post hoc analysis in SigmaPlot 11 scientific graphing and data analysis program (Systat Software Inc.).
AT1 in dopamine neurons, microglia, astrocytes, and vascular smooth muscle cells in the substantia nigra of neurologically and neuropathologically normal patients (AMC) as well as in prePD and PD patients
Loss of dopamine neurons in nigrosome 1 and in the matrix correlates with progression from AMC to prePD to PD
Total cellular AT1 expression in nigral dopamine neurons is reduced with disease progression, but nuclear AT1 in such cells in nigrosome 1 is unchanged
Intranuclear expression of Nox4 in dopamine neurons is associated with intranuclear oxidative damage to nucleic acids and activation of caspase-3
Here, we report that dopamine neurons from intact substantia nigra of neurologically and neuropathologically normal patients (AMC) differ substantially with respect to the levels of AT1 expression as well as intranuclear expression of superoxide-generating Nox4, nuclear oxidative stress, and cellular activation of caspase-3 from clinically asymptomatic patients, who had only modest dopamine cell loss, but had Braak stages that were consistent with a neuropathological diagnosis of PD (referred to here as prePD), and from advanced PD patients. We found that the total cellular AT1 levels were reduced in dopamine neurons of prePD patients as compared to age-matched neurologically normal controls (AMC). Previously, Ge and Barnes  demonstrated reduced radiolabelled AngII binding to the AT1 in tissue extracts from caudate nucleus, putamen, and substantia nigra of Parkinson patients with advanced disease compared to neurologically normal control patients. We established that this general loss of AT1 in substantia nigra is largely due to the reduction of AT1 in dopamine neurons, which led us to speculate that neurons in other basal ganglia structures, namely the caudate and putamen, might also experience a reduction in AT1. In our study, tissue from clinically- and neuropathologically-confirmed PD patients had greater cell loss and greater decline in the total cellular levels of AT1 in surviving dopamine neurons in both the calbindin-rich matrix and in the calbindin-poor nigrosome 1 than was observed in dopamine neurons from prePD patients. This pathology-associated decline in AT1 and the accompanying increase in Nox4 from AMC to prePD and finally to PD is suggestive of a progressive loss of dopamine neurons in nigral matrix and nigrosome 1 due to excess Nox4 generation in the nucleus of dopamine neurons and a consequent increase in production of superoxide at levels that precipitate nucleic acid damage leading to neuronal dysfunction and death.
Even though a combination of insufficient tissue sample to perform unbiased stereological counts for TH+ neurons necessitated counts of all nigral TH+ neurons from just one section per patient and the number of available patients (particularly prePD, n = 3) resulted in relatively high standard errors, the counts of TH+ neurons obtained corresponded closely with the original nigrosome/matrix principles defined by Damier and colleagues , in which loss of nigrosome 1 dopamine neurons is faster than the loss of such neurons in the matrix. In that vein, we observed that in PD as well as in prePD the density of TH+ neurons was markedly and significantly lower in nigrosome 1 as compared with matrix. In addition, and in agreement with the Damier principle , in our patients the density of TH+ neurons was the same in the matrix and nigrosome 1 in AMC and followed a trend of gradual decline with the disease progression. Our observation that the decline in the AT1 expression in the matrix, a structure with a relative to nigrosome 1 sparing of dopamine neurons in PD (Figure 4 and ), is greater than that in the more affected nigrosome 1 where we detected a significant loss of TH+ neurons in both prePD as well as in PD cases, suggests that probability that neurons survive increases in association with lower total (Figure 4) as well as nuclear (Figure 5) AT1 expression.
Nuclear localization of Nox4 has been reported from other cell types such as human vascular endothelial cells  and from cardiomyocytes, in which Nox4 causes histone deacetylase 4 (HDAC4) cysteine oxidation, leading to HDAC4 exit from the nucleus and cardiac hypertrophy . Within nuclei, Nox4 has been reported to localize to speckle domains, i.e., nuclear domains in the interchromatin regions of the nucleus, adjacent to highly transcriptionally active regions, suggesting that Nox4-generated superoxide might be regulating proteins involved in pre-mRNA splicing in these unique nuclear compartments , underscoring the potential for Nox4 to regulate the dynamics of the nuclear gene expression machinery. In addition to its nuclear distribution, Nox4 is often found in the mitochondria in various cell types including neurons . In cardiomyocytes, hypertrophic stimulation increases production of Nox4, which is constitutively active as its activity is principally controlled by its expression levels, which leads to increased superoxide production and mitochondrial dysfunction – events that culminate in apoptosis of cardiomyocytes . An example of the deleterious role of Nox4 in the brain comes from studies of ischemic stroke, where Nox4 is a major source of oxidative stress, a finding supported by the observations that pharmacological as well as genetic inhibition of Nox4 in a mouse model of stroke prevents oxidative stress and neurodegeneration . In addition to its role in oxidation, Nox4 promotes inflammation as reported by Ginnan and colleagues in smooth muscle cells where Nox4 is required for interleukin 1β-mediated activation of protein kinase C and of c-jun N-terminal kinase .
While Nox4 can drive pathogenic pathways when overactive, physiological activation of Nox4 is important for maintenance of many cellular functions, including transcription and proliferation. In that regard, the changes noted here in AngII/AT1/Nox4 and the implicit generation of superoxide, and in 8-OH guanosine and its signature nucleic acid oxidation may have been elicited in an attempt to protect these dopamine neurons, and/or to stimulate regeneration, as has been reported in the leukocyte-dependent regeneration of zebra fish tail fin . Such regeneration is dependent on production of hydrogen peroxide, which in addition to its antiseptic actions, sets up a hydrogen peroxide gradient across the margin of the wound, signaling rapid recruitment of leukocytes, restoration of the epithelial barrier between the injured tissue and the outside environment and pathogens, and stem cell proliferation for fin genesis . However, as exemplified in neurodegenerative diseases in general, such mechanisms may initially be elicited toward restoration of neuronal resilience [28,39] as we have shown previously for AngII/AT1/Nox4-mediated neural stem cell proliferation , but when neuronal stress is prolonged overtime these mechanisms may lead, as our findings indicate here, to oxidative damage and loss of dopamine neurons and the frank neurological and neuropathological manifestations of neurodegenerative diseases such as Alzheimer’s and Parkinson’s.
To investigate the potential for apoptotic neuronal cell death in our AMC, prePD, and PD patients, we determined caspase-3 activation in dopamine neurons across these disease stages. There are strong similarities between historical findings of a temporal relationship between a progressive rise in the levels of cleaved caspase-3 in both the cytoplasmic as well as the nuclear compartments in nigral dopamine neurons in rats injected intrastriatally with 6-OHDA [40,41] and our findings of a stepwise AMC<prePD<PD increase in cleaved caspase-3 in cytoplasm of nigral dopamine neurons that culminated in caspase-3 expression in both cytoplasm and nucleus in frank disease. These historical findings [40,41], together with our findings in human tissue are indicative of an AngII/AT1/Nox4-superoxide axis that contributes to, and thus may be responsible for, the progressive dysfunction and loss of dopaminergic neurons that underlie the neuropathological changes and neurological failures characteristic of Parkinson’s.
Inquest into brain angiotensin-regulated pathways raises a question of why components of RAS are expressed in neurons. Several lines of evidence point to counter-regulation between RAS and dopamine as a principal reason, where, as we hypothesize, the increase in AngII signaling via AT1 might directly promote dopaminergic neurotransmission by increasing the activity of TH, as was demonstrated outside the brain in organs such as the kidney . Additional support for angiotensin↔ dopamine counterregulation comes from experiments in rats, where depletion of dopamine with an inhibitor of TH, reserpine, resulted in an increase in AT1 at both mRNA and protein levels . In parallel experiments in which similar increases in AT1 were achieved with 6-OHDA administration, co-administration of L-dopa prevented such increases in AT1 . In our study, in contrast to the prePD patients who were not treated with L-dopa, in L-dopa-medicated advanced PD patients, the L-dopa treatment might have affected the AT1 expression profiles. One could speculate that such effects could potentially include L-dopa promoting lowering of membrane and cytoplasmic AT1 expression while lacking an effect on the nuclear AT1 – a pattern of AT1 expression changes that we have demonstrated in the current study. Further studies of the L-dopa effects on the RAS are needed to illuminate these important angiotensin↔dopamine counterregulatory mechanisms in the human brain. Such studies should also consider potential contributions of other biological processes on the regulation of AT1 expression. In addition to L-dopa-regulation of AT1 levels, other molecular entities and biological processes affect AT1 levels. For example, elevation of AngII/AT1 also occurs in rodents with: i) advancing age , ii) reduction in estrogen modeling menopause , and iii) hypoperfusion of the brain . Central activity of AngII has also been reported to be elevated in conditions that compromise blood–brain barrier (BBB), such as neurogenic hypertension, permitting circulating AngII access to the CNS . Such effects of the circulating AngII on the CNS were also demonstrated in rats with mannitol-mediated experimental disruption of the BBB, which resulted in circulating AngII gaining access to the rostral ventrolateral medulla; there AngII increased activation of dopamine neurons assayed by an increase in c-Fos immunoreactivity in TH-immunopositive neurons .
The idea of altering the activity of RAS for therapeutic benefit in Parkinson’s was first tested in Melbourne by demonstrating in a prospective study that the angiotensin converting enzyme (ACE) inhibitor, perindopril, reduces levodopa-induced dyskinesias . Subsequently, progress in elucidating the potential role of AngII/AT1 interactions in Parkinson neuropathogenesis has been greatly aided by the development of MPTP- and 6-OHDA-rodent models of Parkinson’s [4,18]. Treatment of rodents with blockers of AT1 (ARBs) before administration of either MPTP or 6-OHDA prevents neurotoxic effects of these agents through less microglial activation, less generation of NADPH oxidase (e.g., Nox4) and therefore less superoxide production, and less neuronal dysfunction and loss, suggesting that ARBs promote dopamine neuron resilience and survival. The insights gained from the rodent studies have now been validated in humans by Lee and colleagues who report in a study of 65,000 neurologically normal hypertensive patients that use of high cumulative doses of ARBs is associated with reduced risk of developing Parkinson’s when compared to the use of β blockers . The beneficial effects of ARBs on human CNS neurons extend beyond Parkinson’s. As a matter of fact, among Alzheimer patients treated with ARBs the incidence of Alzheimer is less and there is less Alzheimer neuropathology [50,51]. Moreover, cognition is improved [50,52].These findings in patients, together with studies of animal models of Parkinson’s and Alzheimer’s [4,18,53], suggest that downregulation of the AngII/AT1-driven cascades may, in general, confer neuronal protection. Whether such interactions are part of the initiation and progression of the neuropathological changes in dopamine neurons that are associated with Parkinson’s is, at present, unclear. Furthermore, if such events are part of Parkinson’s pathogenesis, whether and/or how intervention to modify AngII/AT1 interactions may circumvent or delay onset of Parkinson neuropathogenesis is unknown. To our knowledge, this present report is first to demonstrate the cellular and subcellular distribution of AT1 and Nox4 relative to Parkinson’s disease progression.
Our examination of nuclear morphology showed specific changes that correlated with disease progression. The nucleus is the largest organelle in a dopamine neuron and has intricate connections to the cytoskeleton that maintain topographical and functional nucleo-cytoskeletal interdependence . In addition, changes in nuclear shape and size are associated with diseases such as cancer as well as with aging [55,56]. We have noted a potential disruption of normal nuclear morphology in dopamine neurons coincident with accumulations of aberrantly-expressed assemblies containing nuclear deposits of AT1 and Nox4 infiltrating deep into the nuclei of affected dopamine neurons. In most such affected neurons, these AT1/Nox4 accumulations infiltrate nuclei from only one side along the nuclear long axis. Whether such nuclear accumulations disrupt structure-dependent molecular interactions and gene expression profiles by destabilizing normal regulation of nuclear processes such as molecular crowding, which controls diffusion and interactions of nuclear proteins with heterochromatin [57,58], and thereby accelerate the advance of neurodegenerative disease pathology and neuronal dysfunction, is unknown. By analogy to our findings of AT1/Nox4 intranuclear accumulations, filamentous tau deposits that span the nuclear long axis and are referred to as “tau nuclear rods” have been reported from neurons in the striatum and in the cortex of Huntington patients and in the hippocampal neurons in Alzheimer patients . Although tau nuclear rods are hypothesized by some to be harmless signatures of altered microtubule dynamics, other investigators propose that tau nuclear rods could compromise the integrity of the nuclear membrane promoting nuclear fragmentation and cell death . The previously unrecognized patterns of proportional increases in nuclear AT1 in dopamine neurons in nigrosome 1 of prePD and PD patients that we observed might underscore a surge in neurooxidative and neuroinflammatory processes favoring increased intranuclear stress and oxidative damage to nucleic acids leading to promulgation of untoward transcriptional changes. Hypothetically, such aberrant nuclei could arise from the disease process-related topographic modulation of the nuclear shape – a feature that might serve as a surrogate of pathologic progression in Parkinson’s. Future studies of AT1/Nox4 nuclear buildup should examine changes to the nuclear geometry and nucleo-cytoskeletal dynamics using quantitative nuclear morphometry and interrogate these nuclear features for association with changes in gene expression patterns.
Unlike many studies that report expression changes from only subjective ranking or from small numbers of cells, we have dedicated a substantial effort to assure that AT1 expression was measured in a highly controlled and reproducible fashion in a large number of TH+ neurons. The quantification method employed by us utilized Nikon Element’s data analysis software intensity measurements that have been used and confirmed against other methods for protein expression analysis (Western immunoblot and ELISA) by us and other groups and published in a number of reports [26,28,60]. In addition, detailed examination by two blinded evaluators of the computer-generated AT1 signal intensity measured corresponded reliably with the visual examination of the same cells in corresponding photomicrographs. Despite a series of important changes in expression and localization of AT1 that we found to be associated with disease progression, our study has limitations including low numbers of prePD patients (n = 3) and use of immunohistofluorescence as a sole method for AT1 quantification. Practical reasons including the fact that presymptomatic patients demonstrating Braak stages and dopamine neuron loss consistent with early PD are difficult to find and that the brain tissues from these patients were available only in the form of paraffin-embedded tissue blocks necessitated the present study design. Future studies will focus on identification of a larger cohort of prePD patients in whom RAS-related biomarkers of early disease can be examined further using in addition to immunohistochemical methods, multiplex gene expression profiling and biochemical protein analysis approaches.
The evolutionary advantage of increasing AngII/AT1 activity might reflect the brain’s attempt to counteract the deficits in dopaminergic neurotransmission that accompany progression of Parkinson’s disease, and concurrently, via the AngII/AT1/Nox4 pathway increase neurogenesis as a measure to replace neurons being lost. Our current study and earlier investigations in animal models as well as by means of clinical studies with ARBs demonstrated a fundamental role for the AT1 in Parkinson’s and Alzheimer’s, but as of yet have not explored other molecular players in the complex network of brain RAS. These players include at least four other angiotensins (AngIII, AngIV, Ang1–7, and Ang3–7) in addition to AngII; another ACE, namely ACE2; as well as four additional receptors, namely AT2, AT4, Mas, and pro-renin receptors, extending substantially the RAS-related receptor field beyond the AT1 (for review see ). Although examination of these additional components of RAS was certainly beyond the scope of the current study, investigations that will take place during the next decade will offer novel insights into the complex regulation of the brain RAS and will engineer means for modulating RAS activity for disease-modification or perhaps even prevention in Parkinson’s, Alzheimer’s, and beyond.
Using semiquantitative immunohistofluorescence, we found that AT1 protein expression in dopamine neurons of the human substantia nigra is reduced with the disease progression from AMC → prePD → PD in the calbindin-rich matrix and in the calbindin-poor nigrosome 1, where we observed greater loss of TH-immunopositive dopamine neurons. In all cases examined, the AT1 was primarily associated with the intracellular structures within the cytoplasm as well as with the nuclear envelope and nuclear pore complexes, as determined by colocalization of the AT1 with nucleoporin p62, and deep within the nuclei of dopamine neurons. Although the nuclear AT1 in dopamine neurons located in the matrix demonstrated a similar loss of AT1 corresponding with the clinicopathological progression as was observed for the entire neuron AT1, the nuclear AT1 in the nigrosome 1 dopamine neurons did not show reduction and remained at levels characteristic of the neurologically and neuropathologically normal control patients. Therefore, we propose that such a nonphysiological shift in the cytoplasmic and nuclear AT1 distribution in favor of nuclear AT1 increases oxidative damage to DNA. Such a scenario is supported by the observed colocalization of the nuclear AT1 with superoxide-generating Nox4 and with 8-OH guanosine-detected oxidative damage to the nucleic acids. Disease progression from AMC → prePD → PD was also associated with increases in Nox4, oxidative damage to DNA, and activation of caspase-3 in the nuclei of dopamine neurons, giving support to the idea that an AngII/AT1/Nox4-superoxide axis contributes to the neurooxidative injury in dopamine neurons and underscoring the need for further studies of modifiers of the brain RAS activity for preventive and/or symptomatic treatment of neurodegenerative diseases.
Authors thank John DeFelice, Imperial College London, for performing α-synuclein immunohistochemistry necessary for Braak staging. This work was supported by the NIH AG12411 grant (WSTG and SMG), the Inglewood Foundation (WMZ), and the Windgate Foundation (WSTG and OA).
- Schelling P, Hutchinson JS, Ganten U, Sponer G, Ganten D (1976) Impermeability of the blood-cerebrospinal fluid barrier for angiotensin II in rats. Clin Sci Mol Med Suppl 3:399s–402PubMedGoogle Scholar
- Jiang T, Gao L, Lu J, Zhang YD (2013) ACE2-Ang-(1–7)-mas axis in brain: a potential target for prevention and treatment of ischemic stroke. Curr Neuropharmacol 11(2):209–17, doi:10.2174/1570159X11311020007PubMed CentralPubMedView ArticleGoogle Scholar
- Griendling KK, Minieri CA, Ollerenshaw JD, Alexander RW (1994) Angiotensin II stimulates NADH and NADPH oxidase activity in cultured vascular smooth muscle cells. Circ Res 74(6):1141–8PubMedView ArticleGoogle Scholar
- Grammatopoulos TN, Jones SM, Ahmadi FA, Hoover BR, Snell LD, Skoch J et al (2007) Angiotensin type 1 receptor antagonist losartan, reduces MPTP-induced degeneration of dopaminergic neurons in substantia nigra. Mol Neurodegener 2:1, doi:10.1186/1750-1326-2-1PubMed CentralPubMedView ArticleGoogle Scholar
- Garrido-Gil P, Valenzuela R, Villar-Cheda B, Lanciego JL, Labandeira-Garcia JL (2013) Expression of angiotensinogen and receptors for angiotensin and prorenin in the monkey and human substantia nigra: an intracellular renin-angiotensin system in the nigra. Brain Struct Funct 218(2):373–88, doi:10.1007/s00429-012-0402-9PubMed CentralPubMedView ArticleGoogle Scholar
- Deliu E, Brailoiu GC, Eguchi S, Hoffman NE, Rabinowitz JE, Tilley DG et al (2014) Direct evidence of intracrine angiotensin II signaling in neurons. Am J Physiol Cell Physiol 306(8):C736–44, doi:10.1152/ajpcell.00131.2013PubMedView ArticleGoogle Scholar
- Erdmann B, Fuxe K, Ganten D (1996) Subcellular localization of angiotensin II immunoreactivity in the rat cerebellar cortex. Hypertension 28(5):818–24PubMedView ArticleGoogle Scholar
- Robertson AL Jr, Khairallah PA (1971) Angiotensin II: rapid localization in nuclei of smooth and cardiac muscle. Science 172(3988):1138–9PubMedView ArticleGoogle Scholar
- O’Callaghan EL, Choong YT, Jancovski N, Allen AM (2013) Central angiotensinergic mechanisms associated with hypertension. Auton Neurosci 175(1–2):85–92, doi:10.1016/j.autneu.2013.01.010PubMedView ArticleGoogle Scholar
- Simonnet G, Giorguieff-Chesselet MF (1979) Stimulating effect of angiotensin II on the spontaneous release of newly synthetized [3H]dopamine in rat striatal slices. Neurosci Lett 15(2–3):153–8PubMedView ArticleGoogle Scholar
- Mendelsohn FA, Jenkins TA, Berkovic SF (1993) Effects of angiotensin II on dopamine and serotonin turnover in the striatum of conscious rats. Brain Res 613(2):221–9PubMedView ArticleGoogle Scholar
- Topchiy E, Panzhinskiy E, Griffin WS, Barger SW, Das M, Zawada WM (2013) Nox4-generated superoxide drives angiotensin II-induced neural stem cell proliferation. Dev Neurosci 35(4):293–305, doi:10.1159/000350502PubMed CentralPubMedView ArticleGoogle Scholar
- Rodriguez-Pallares J, Quiroz CR, Parga JA, Guerra MJ, Labandeira-Garcia JL (2004) Angiotensin II increases differentiation of dopaminergic neurons from mesencephalic precursors via angiotensin type 2 receptors. Eur J Neurosci 20(6):1489–98PubMedView ArticleGoogle Scholar
- Allen AM, MacGregor DP, Chai SY, Donnan GA, Kaczmarczyk S, Richardson K et al (1992) Angiotensin II receptor binding associated with nigrostriatal dopaminergic neurons in human basal ganglia. Ann Neurol 32(3):339–44, doi:10.1002/ana.410320306PubMedView ArticleGoogle Scholar
- Allen AM, Paxinos G, McKinley MJ, Chai SY, Mendelsohn FA (1991) Localization and characterization of angiotensin II receptor binding sites in the human basal ganglia, thalamus, midbrain pons, and cerebellum. J Comp Neurol 312(2):291–8, doi:10.1002/cne.903120211PubMedView ArticleGoogle Scholar
- Joglar B, Rodriguez-Pallares J, Rodriguez-Perez AI, Rey P, Guerra MJ, Labandeira-Garcia JL (2009) The inflammatory response in the MPTP model of Parkinson’s disease is mediated by brain angiotensin: relevance to progression of the disease. J Neurochem 109(2):656–69, doi:10.1111/j.1471-4159.2009.05999.xPubMedView ArticleGoogle Scholar
- Villar-Cheda B, Valenzuela R, Rodriguez-Perez AI, Guerra MJ, Labandeira-Garcia JL (2012) Aging-related changes in the nigral angiotensin system enhances proinflammatory and pro-oxidative markers and 6-OHDA-induced dopaminergic degeneration. Neurobiol Aging 33(1):204 e201-211, doi:10.1016/j.neurobiolaging.2010.08.006View ArticleGoogle Scholar
- Rey P, Lopez-Real A, Sanchez-Iglesias S, Munoz A, Soto-Otero R, Labandeira-Garcia JL (2007) Angiotensin type-1-receptor antagonists reduce 6-hydroxydopamine toxicity for dopaminergic neurons. Neurobiol Aging 28(4):555–67, doi:10.1016/j.neurobiolaging.2006.02.018PubMedView ArticleGoogle Scholar
- Zawada WM, Banninger GP, Thornton J, Marriott B, Cantu D, Rachubinski AL et al (2011) Generation of reactive oxygen species in 1-methyl-4-phenylpyridinium (MPP+) treated dopaminergic neurons occurs as an NADPH oxidase-dependent two-wave cascade. J Neuroinflammation 8:129, doi:10.1186/1742-2094-8-129PubMed CentralPubMedView ArticleGoogle Scholar
- Rodriguez-Pallares J, Parga JA, Munoz A, Rey P, Guerra MJ, Labandeira-Garcia JL (2007) Mechanism of 6-hydroxydopamine neurotoxicity: the role of NADPH oxidase and microglial activation in 6-hydroxydopamine-induced degeneration of dopaminergic neurons. J Neurochem 103(1):145–56, doi:10.1111/j.1471-4159.2007.04699.xPubMedGoogle Scholar
- Ge J, Barnes NM (1996) Alterations in angiotensin AT1 and AT2 receptor subtype levels in brain regions from patients with neurodegenerative disorders. Eur J Pharmacol 297(3):299–306PubMedView ArticleGoogle Scholar
- Damier P, Hirsch EC, Agid Y, Graybiel AM (1999) The substantia nigra of the human brain. I. Nigrosomes and the nigral matrix, a compartmental organization based on calbindin D(28K) immunohistochemistry. Brain 122(Pt 8):1421–36PubMedView ArticleGoogle Scholar
- Damier P, Hirsch EC, Agid Y, Graybiel AM (1999) The substantia nigra of the human brain. II. Patterns of loss of dopamine-containing neurons in Parkinson’s disease. Brain 122(Pt 8):1437–48PubMedView ArticleGoogle Scholar
- Alafuzoff I, Ince PG, Arzberger T, Al-Sarraj S, Bell J, Bodi I et al (2009) Staging/typing of Lewy body related alpha-synuclein pathology: a study of the BrainNet Europe Consortium. Acta Neuropathol 117(6):635–52, doi:10.1007/s00401-009-0523-2PubMedView ArticleGoogle Scholar
- McKeith IG, Dickson DW, Lowe J, Emre M, O’Brien JT, Feldman H et al (2005) Diagnosis and management of dementia with Lewy bodies: third report of the DLB Consortium. Neurology 65(12):1863–72PubMedView ArticleGoogle Scholar
- Aboud O, Mrak RE, Boop F, Griffin ST (2012) Apolipoprotein epsilon 3 alleles are associated with indicators of neuronal resilience. BMC Med 10(1):35, doi:10.1186/1741-7015-10-35PubMed CentralPubMedView ArticleGoogle Scholar
- Barger SW, DeWall KM, Liu L, Mrak RE, Griffin WS (2008) Relationships between expression of apolipoprotein E and beta-amyloid precursor protein are altered in proximity to Alzheimer beta-amyloid plaques: potential explanations from cell culture studies. J Neuropathol Exp Neurol 67(8):773–83, doi:10.1097/NEN.0b013e318180ec47PubMed CentralPubMedView ArticleGoogle Scholar
- Aboud O, Mrak RE, Boop FA, Griffin WS (2013) Epilepsy: neuroinflammation, neurodegeneration, and APOE genotype. Acta Neuropathol Commun 1(1):41, doi:10.1186/2051-5960-1-41PubMed CentralPubMedView ArticleGoogle Scholar
- Tadevosyan A, Maguy A, Villeneuve LR, Babin J, Bonnefoy A, Allen BG et al (2010) Nuclear-delimited angiotensin receptor-mediated signaling regulates cardiomyocyte gene expression. J Biol Chem 285(29):22338–49, doi:10.1074/jbc.M110.121749PubMed CentralPubMedView ArticleGoogle Scholar
- Davis LI, Blobel G (1986) Identification and characterization of a nuclear pore complex protein. Cell 45(5):699–709PubMedView ArticleGoogle Scholar
- Matsushima S, Kuroda J, Ago T, Zhai P, Park JY, Xie LH et al (2013) Increased oxidative stress in the nucleus caused by Nox4 mediates oxidation of HDAC4 and cardiac hypertrophy. Circ Res 112(4):651–63, doi:10.1161/CIRCRESAHA.112.279760PubMed CentralPubMedView ArticleGoogle Scholar
- Guida M, Maraldi T, Beretti F, Follo MY, Manzoli L, De Pol A (2014) Nuclear nox4-derived reactive oxygen species in myelodysplastic syndromes. Biomed Res Int 2014:456937, doi:10.1155/2014/456937PubMed CentralPubMedView ArticleGoogle Scholar
- Kuroda J, Nakagawa K, Yamasaki T, Nakamura K, Takeya R, Kuribayashi F et al (2005) The superoxide-producing NAD(P)H oxidase Nox4 in the nucleus of human vascular endothelial cells. Genes Cells 10(12):1139–51, doi:10.1111/j.1365-2443.2005.00907.xPubMedView ArticleGoogle Scholar
- Case AJ, Li S, Basu U, Tian J, Zimmerman MC (2013) Mitochondrial-localized NADPH oxidase 4 is a source of superoxide in angiotensin II-stimulated neurons. Am J Physiol Heart Circ Physiol 305(1):H19–28, doi:10.1152/ajpheart.00974.2012PubMed CentralPubMedView ArticleGoogle Scholar
- Ago T, Kuroda J, Pain J, Fu C, Li H, Sadoshima J (2010) Upregulation of Nox4 by hypertrophic stimuli promotes apoptosis and mitochondrial dysfunction in cardiac myocytes. Circ Res 106(7):1253–64, doi:10.1161/CIRCRESAHA.109.213116PubMed CentralPubMedView ArticleGoogle Scholar
- Kleinschnitz C, Grund H, Wingler K, Armitage ME, Jones E, Mittal M, Barit D, Schwarz T, Geis C, Kraft P, Barthel K, Schuhmann MK, Herrmann AM, Meuth SG, Stoll G, Meurer S, Schrewe A, Becker L, Gailus-Durner V, Fuchs H, Klopstock T, de Angelis MH, Jandeleit-Dahm K, Shah AM, Weissmann N, Schmidt HH (2010) Post-stroke inhibition of induced NADPH oxidase type 4 prevents oxidative stress and neurodegeneration. PLoS Biology 8(9). doi:10.1371/journal.pbio.1000479
- Ginnan R, Jourd’heuil FL, Guikema B, Simons M, Singer HA, Jourd’heuil D (2013) NADPH oxidase 4 is required for interleukin-1beta-mediated activation of protein kinase Cdelta and downstream activation of c-jun N-terminal kinase signaling in smooth muscle. Free Radic Biol Med 54:125–34, doi:10.1016/j.freeradbiomed.2012.09.026PubMed CentralPubMedView ArticleGoogle Scholar
- Niethammer P, Grabher C, Look AT, Mitchison TJ (2009) A tissue-scale gradient of hydrogen peroxide mediates rapid wound detection in zebrafish. Nature 459(7249):996–9, doi:10.1038/nature08119PubMed CentralPubMedView ArticleGoogle Scholar
- Wilcock DM (2012) Neuroinflammation in the aging Down syndrome brain; lessons from Alzheimer’s disease. Curr Gerontol Geriatr Res 2012:170276, doi:10.1155/2012/170276PubMed CentralPubMedGoogle Scholar
- Hernandez-Baltazar D, Mendoza-Garrido ME, Martinez-Fong D (2013) Activation of GSK-3beta and caspase-3 occurs in Nigral dopamine neurons during the development of apoptosis activated by a striatal injection of 6-hydroxydopamine. PLoS One 8(8):e70951, doi:10.1371/journal.pone.0070951PubMed CentralPubMedView ArticleGoogle Scholar
- Oo TF, Siman R, Burke RE (2002) Distinct nuclear and cytoplasmic localization of caspase cleavage products in two models of induced apoptotic death in dopamine neurons of the substantia nigra. Exp Neurol 175(1):1–9, doi:10.1006/exnr.2002.7881PubMedView ArticleGoogle Scholar
- Labandeira-Garcia JL, Rodriguez-Pallares J, Villar-Cheda B, Rodriguez-Perez AI, Garrido-Gil P, Guerra MJ (2011) Aging, angiotensin system and dopaminergic degeneration in the substantia nigra. Aging Dis 2(3):257–74PubMed CentralPubMedGoogle Scholar
- Villar-Cheda B, Rodriguez-Pallares J, Valenzuela R, Munoz A, Guerra MJ, Baltatu OC et al (2010) Nigral and striatal regulation of angiotensin receptor expression by dopamine and angiotensin in rodents: implications for progression of Parkinson’s disease. Eur J Neurosci 32(10):1695–706, doi:10.1111/j.1460-9568.2010.07448.xPubMedView ArticleGoogle Scholar
- Rodriguez-Perez AI, Valenzuela R, Villar-Cheda B, Guerra MJ, Labandeira-Garcia JL (2012) Dopaminergic neuroprotection of hormonal replacement therapy in young and aged menopausal rats: role of the brain angiotensin system. Brain 135(Pt 1):124–38, doi:10.1093/brain/awr320PubMedView ArticleGoogle Scholar
- Rodriguez-Perez AI, Dominguez-Meijide A, Lanciego JL, Guerra MJ, Labandeira-Garcia JL (2013) Dopaminergic degeneration is enhanced by chronic brain hypoperfusion and inhibited by angiotensin receptor blockage. Age 35(5):1675–90, doi:10.1007/s11357-012-9470-2PubMed CentralPubMedView ArticleGoogle Scholar
- Biancardi VC, Son SJ, Ahmadi S, Filosa JA, Stern JE (2014) Circulating angiotensin II gains access to the hypothalamus and brain stem during hypertension via breakdown of the blood–brain barrier. Hypertension 63(3):572–9, doi:10.1161/HYPERTENSIONAHA.113.01743PubMed CentralPubMedView ArticleGoogle Scholar
- Yao ST, May CN (2013) Intra-carotid angiotensin II activates tyrosine hydroxylase-expressing rostral ventrolateral medulla neurons following blood–brain barrier disruption in rats. Neuroscience 245:148–56, doi:10.1016/j.neuroscience.2013.04.023PubMedView ArticleGoogle Scholar
- Reardon KA, Mendelsohn FA, Chai SY, Horne MK (2000) The angiotensin converting enzyme (ACE) inhibitor, perindopril, modifies the clinical features of Parkinson’s disease. Aust NZ J Med 30(1):48–53View ArticleGoogle Scholar
- Lee YC, Lin CH, Wu RM, Lin JW, Chang CH, Lai MS (2014) Antihypertensive agents and risk of Parkinson’s disease: a nationwide cohort study. PLoS One 9(6):e98961, doi:10.1371/journal.pone.0098961PubMed CentralPubMedView ArticleGoogle Scholar
- Li NC, Lee A, Whitmer RA, Kivipelto M, Lawler E, Kazis LE et al (2010) Use of angiotensin receptor blockers and risk of dementia in a predominantly male population: prospective cohort analysis. BMJ 340:b5465, doi:10.1136/bmj.b5465PubMed CentralPubMedView ArticleGoogle Scholar
- Hajjar I, Brown L, Mack WJ, Chui H (2012) Impact of Angiotensin receptor blockers on Alzheimer disease neuropathology in a large brain autopsy series. Arch Neurol 69(12):1632–8, doi:10.1001/archneurol.2012.1010PubMed CentralPubMedView ArticleGoogle Scholar
- Li W, Zhang JW, Lu F, Ma MM, Wang JQ, Suo AQ et al (2012) Effects of telmisartan on the level of Abeta1-42, interleukin-1beta, tumor necrosis factor alpha and cognition in hypertensive patients with Alzheimer’s disease. Zhonghua Yi Xue Za Zhi 92(39):2743–6PubMedGoogle Scholar
- Danielyan L, Klein R, Hanson LR, Buadze M, Schwab M, Gleiter CH et al (2010) Protective effects of intranasal losartan in the APP/PS1 transgenic mouse model of Alzheimer disease. Rejuvenation Res 13(2–3):195–201, doi:10.1089/rej.2009.0944PubMedView ArticleGoogle Scholar
- Ramdas NM, Shivashankar GV (2014) Cytoskeletal Control of Nuclear Morphology and Chromatin Organization. J Mol Biol. doi:10.1016/j.jmb.2014.09.008
- Edens LJ, White KH, Jevtic P, Li X, Levy DL (2013) Nuclear size regulation: from single cells to development and disease. Trends Cell Biol 23(4):151–9, doi:10.1016/j.tcb.2012.11.004PubMedView ArticleGoogle Scholar
- Jevtic P, Edens LJ, Vukovic LD, Levy DL (2014) Sizing and shaping the nucleus: mechanisms and significance. Curr Opin Cell Biol 28:16–27, doi:10.1016/j.ceb.2014.01.003PubMedView ArticleGoogle Scholar
- Woringer M, Darzacq X, Izeddin I (2014) Geometry of the nucleus: a perspective on gene expression regulation. Curr Opin Chem Biol 20:112–9, doi:10.1016/j.cbpa.2014.05.009PubMedView ArticleGoogle Scholar
- Bancaud A, Huet S, Daigle N, Mozziconacci J, Beaudouin J, Ellenberg J (2009) Molecular crowding affects diffusion and binding of nuclear proteins in heterochromatin and reveals the fractal organization of chromatin. EMBO J 28(24):3785–98, doi:10.1038/emboj.2009.340PubMed CentralPubMedView ArticleGoogle Scholar
- Fernandez-Nogales M, Cabrera JR, Santos-Galindo M, Hoozemans JJ, Ferrer I, Rozemuller AJ et al (2014) Huntington’s disease is a four-repeat tauopathy with tau nuclear rods. Nat Med 20(8):881–5, doi:10.1038/nm.3617PubMedView ArticleGoogle Scholar
- Liu L, Aboud O, Jones RA, Mrak RE, Griffin WS, Barger SW (2011) Apolipoprotein E expression is elevated by interleukin 1 and other interleukin 1-induced factors. J Neuroinflammation 8:175, doi:10.1186/1742-2094-8-175PubMed CentralPubMedView ArticleGoogle Scholar
- Wright JW, Kawas LH, Harding JW (2013) A role for the brain RAS in Alzheimer’s and Parkinson’s diseases. Front Endocrinol 4:158, doi:10.3389/fendo.2013.00158Google Scholar
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