Alpha-synuclein aggregates are phosphatase resistant

Alpha-synuclein (αsyn) is an intrinsically disordered protein that aggregates in the brain in several neurodegenerative diseases collectively called synucleinopathies. Phosphorylation of αsyn at serine 129 (PSER129) was considered rare in the healthy human brain but is enriched in pathological αsyn aggregates and is used as a specific marker for disease inclusions. However, recent observations challenge this assumption by demonstrating that PSER129 results from neuronal activity and can be readily detected in the non-diseased mammalian brain. Here, we investigated experimental conditions under which two distinct PSER129 pools, namely endogenous-PSER129 and aggregated-PSER129, could be detected and differentiated in the mammalian brain. Results showed that in the wild-type (WT) mouse brain, perfusion fixation conditions greatly influenced the detection of endogenous-PSER129, with endogenous-PSER129 being nearly undetectable after delayed perfusion fixation (30-min and 1-h postmortem interval). Exposure to anesthetics (e.g., Ketamine or xylazine) before perfusion did not significantly influence endogenous-PSER129 detection or levels. In situ, non-specific phosphatase calf alkaline phosphatase (CIAP) selectively dephosphorylated endogenous-PSER129 while αsyn preformed fibril (PFF)-seeded aggregates and genuine disease aggregates (Lewy pathology and Papp–Lantos bodies in Parkinson’s disease and multiple systems atrophy brain, respectively) were resistant to CIAP-mediated dephosphorylation. The phosphatase resistance of aggregates was abolished by sample denaturation, and CIAP-resistant PSER129 was closely associated with proteinase K (PK)-resistant αsyn (i.e., a marker of aggregation). CIAP pretreatment allowed for highly specific detection of seeded αsyn aggregates in a mouse model that accumulates non-aggregated-PSER129. We conclude that αsyn aggregates are impervious to phosphatases, and CIAP pretreatment increases detection specificity for aggregated-PSER129, particularly in well-preserved biological samples (e.g., perfusion fixed or flash-frozen mammalian tissues) where there is a high probability of interference from endogenous-PSER129. Our findings have important implications for the mechanism of PSER129-accumulation in the synucleinopathy brain and provide a simple experimental method to differentiate endogenous-from aggregated PSER129. Supplementary Information The online version contains supplementary material available at 10.1186/s40478-024-01785-0.


Introduction
Synucleinopathies are age-related neurodegenerative diseases, including Parkinson's disease (PD), Dementia with Lewy bodies (DLB), and Multiple System Atrophy (MSA), where the prominent neuropathological hallmark is aggregates of misfolded alpha-synuclein (αsyn) protein [1].Numerous potential mechanisms for αsyn aggregation have been described, but many details remain unclear, particularly within the human diseased brain.Understanding cellular and molecular mechanisms driving αsyn misfolding and aggregation is fundamental for understanding synucleinopathy disease origins and progression.
PSER129 detection in the healthy mammalian brain (i.e., endogenous-PER129) has been inconsistent across studies [7,8,15,16] with varying abundance, cellular localization, and regional distribution.We observed high variability in the steady-state level of endogenous-PSER129, which could be explained by either sample preparation or biological factors such as neuronal activity [5,6].Protein phosphorylation is highly dynamic, cycling between phosphorylation and dephosphorylated forms on short timescales, and as a result, accurate measurement of PTM's require that biological processes in tissues are rapidly inhibited following death whether by perfusion fixation or other techniques (e.g., flash freezing, small molecule enzyme inhibitors, etc.) [17,18].Whether the observed variability in endogenous-PSER129 levels was due to protocol differences or an unknown biological variable is unclear.
Differentiating endogenous-PSER129 and aggregated-PSER129 is crucial for understanding PSER129's role in αsyn biology and disease.Commercially available PSER129 antibodies have been systematically tested, and EP1536Y (Abcam Cat# ab51253, RRID: AB_869973) has emerged as one of the most specific antibodies for PSER129 [15,16].However, this conclusion depends on assay conditions [7], and with abundant endogenous-PSER129, particularly in preclinical models, PSER129 immunoreactivity alone does not alone identify αsyn aggregates.Endogneous-PSER129 labeling in the brain is often incorrectly described as "diffuse, " but several brain regions and cell types display strong punctate PSER129 reactivity, which could be mistaken for pathogenic aggregates [7], resulting in false positives.Endogenous-PSER129 may also increase the likelihood of false negatives, as signal amplification methods cannot be fully utilized due to "background" from the endogenous population, which obscures detection [19].Limited protease digestion enhances specificity for the immunodetection of αsyn aggregates [20], including when using antibodies against PSER129 [19].However, proteases cleave peptide bonds, severely damaging the specimen integrity, limiting practical utility, and impeding downstream assays such as mass spectrometry [21].

Rapid perfusion fixation preserves endogenous-PSER129
To investigate why endogenous-PSER129 detection has been variable across studies, we performed delayed perfusion fixation of CO 2 euthanized mice.To do this, after euthanasia by CO 2 , we immediately removed the animal's blood by perfusion with PBS and then delayed the time until perfusion with PFA was initiated.We found PSER129 was readily detectable and abundant in brain regions we have previously described [7] in mice rapidly perfused after death (< 30 s) (Fig. 1A, B).In contrast, 30-min delayed perfusion dramatically reduced PSER129, with only a few PSER129 positive nuclei being detectable in a few brain regions, including the OB mitral cell layer (MCL).Similarly, 60-min delayed perfusion resulted in reduced PSER129 staining, with weak reactivity in some cell nuclei of the OB.Quantitative western blots showed that the total amount of αsyn was not significantly altered following delayed perfusion fixation, but PSER129 levels were markedly reduced (F(2,9) = 130.73, p < 0.0001) at 30-min delayed (Optimal vs. 30-min, − 95.7% ± 6.8), and 60-min (Optimal vs. 60-min, − 95.5% ± 6.8) (Fig. 1C-E).The distribution of total protein looked similar between all samples (Fig. 1C, left panel).

Anesthesia exposure does not influence PSER129 abundance
Ketamine and xylazine are commonly used anesthetics for perfusion and fixation and this procedure could potentially influence endogenous-PSER129 via their effects on neuronal activity [29,30] or hypothermia [31].To determine if either anesthetic influenced endogenous-PSER129 detection, we performed perfusion fixation on mice acutely exposed to ketamine (100 mg/kg) xylazine (10 mg/kg) 10 min prior to CO 2 -mediated euthanization and perfusion fixation.Results showed that regardless of anesthesia exposure, no significant difference in endogenous-PSER129 content was detected in the mouse OB.IHC detection of PSER129 was similar between groups (Fig. 1F).Quantitative western blot of proteins extracted from PFA-fixed brain sections encompassing the entire brain (Fig. 1G) showed that the amount of αsyn (Fig. 1H), PSER129 (Fig. 1I), or the ratio of PSER129/αsyn (Fig. 1J), did not significantly differ between anesthetic treatments.PSER129 and αsyn quantities were not significantly correlated (Fig. 1K).

Aggregated-PSER129 selectively resists in situ dephosphorylation in WT mice
To determine if endogenous-PSER129 could be differentiated from aggregated-PSER129, we pretreated brain tissues from OB-PFF-injected mice with calf intestine alkaline phosphatase (CIAP).Without CIAP treatment, PSER129 staining was observed as before [7] throughout the neuroaxis of mice treated with PBS and PFFs (Fig. 2A-C).For OB-PFF mice, in pathology-bearing regions (e.g., OB, EC, AMYG) aggregated-PSER129 was difficult to discern from non-aggregated endogenous-PSER129, except for regions where endogenous-PSER129 levels were relatively low (e.g., GCL).CIAP pretreatment resulted in the abolishment of PSER129 staining in PBS mice, while clear PSER129-positive processes and concentric bodies were observed in selected brain regions of OB-PFF mice, consistent with aggregation seen in the OB-PFF model [19,22,32].CIAP-resistant PSER129 was observed in the MCL of OB-PFF mice, which was obscured entirely by endogenous-PSER129 when CIAP was not used (Fig. 2C).We tested several proteases, but despite having predicted cleavage sites adjacent to αsyn Ser129, they did not wholly abolish PSER129 staining in the PBS mice (Additional file 2: Fig. S1).PK can eliminate endogenous-PSER129 [19] (Additional file 2: Fig. S1), but the treatment is highly destructive, limiting its compatibility with common downstream techniques (LC-MSbased peptide identification).CIAP is nondestructive and effective and should be the preferred approach to differentiate non-aggregated vs. aggregated-PSER129.Thresholding was performed on OB images (Fig. 2D), and the PSER129 area was calculated (Fig. 2E).Overall, a significant decrease in PSER129 was observed after CIAP pretreatment (F(1,4) = 131.2,p = 0.0003).Furthermore, following CIAP treatment, PSER129 was higher in PFF-treated mice than in PBS-treated mice (p = 0.0045).In contrast, without CIAP, no significant differences were detected between PBS and PFF treated mice.

Aggregated-PSER129 selectively resists in situ dephosphorylation in M83 mutant mice
Mice overexpressing human A53T αsyn under the prion promoter (i.e., M83) are a common model for studying αsyn aggregation [33] as they accumulate PSER129 throughout the brain after ~ three months of age [7,27] but do not develop widespread filamentous αsyn aggregates until around ten months of age with the brain stem being most severely affected [25,33].M83 mice injected with extracts from diseased brains or αsyn PFFs develop pathology within a few months of the injection and have an accelerated disease phenotype [25].Because the M83 mouse brain has high quantities of PSER129 prior to aggregation, differentiation between aggregated-PSER129 and endogenous-PSER129 is challenging and can impede accurate assessment of aggregation in this model.
Here we tested whether CIAP treatment could differentiate abundant nonaggregated-PSER129 from aggregate-PSER129 in homozygous M83 mice injected with PFFs unilaterally into the OB.Results showed that without CIAP, ubiquitous PSER129 reactivity was observed in both the injected and noninjected hemispheres (Fig. 3A).In the OB and PA, PSER129 reactivity was similar, with a few dysmorphic neurites being observable (Fig. 3A, B).However, following CIAP pretreatment, the PSER129 reactivity was restricted to the GCL of the injected OB (Fig. 3A).In PA-containing sections just posterior to the OB injection site, diffuse weak PSER129 reactivity was observed, with asymmetrical PSER129 signal in the PA of the injected hemisphere (Fig. 3A, red outline).High magnification images revealed that following CIAP nondiffuse PSER129 reactivity could be observed only in the GCL and PA of PFF-treated mice (Fig. 3B).Reactivity was strong in those regions and morphologically resembled neuronal processes and cell bodies, in contrast to PBS treated mice, which lacked PSER129 reactivity.
To determine the degree of CIAP resistance of apparent aggregated-PSER129, we treated tissues from OB-PFF M83 mice with CIAP for 16 h and 70 h.We found that PSER129 reactivity remained in PA even after several days (70 h) of CIAP exposure (Fig. 3C).These results suggest that αsyn aggregates are impervious to CIAPmediated dephosphorylation.We did not test time points greater than 70 h.Threshold masking and object area analysis were used to quantify CIAP-resistant and CIAPsensitive PSER129 (Fig. 3D) under different CIAP conditions.Results show that in the PBS-injected OB, CIAP pretreatment (16 h and 70 h) resulted in a total loss of PSER129 immuno-reactivity (Fig. 3E).Following CIAP, PSER129 staining significantly differed between PBS and PFF-treated mice; in contrast, without CIAP, PSER129 was the same between PBS and PFF (Additional file 2: Fig. S3).
Results using EPR20535 showed that PK-αsyn overlaps well with CIAP-PSER129 in the OB and PA (Fig. 4).

αSyn aggregates in human synucleinopathy brain resist in situ dephosphorylation
PSER129 is a selective, sensitive marker for pathology in the synucleinopathy brain, as endogenous-PSER129 levels are considered low in the non-synucleinopathy brain.
Because we found aggregated-PSER129 was impervious PK-asyn CIAP-PSER129 Overlay C B to CIAP-mediated dephosphorylation in PFF models, we tested the hypothesis that αsyn aggregates in the human brain were CIAP resistant.We stained PSER129 in PD (Fig. 5A, C) and MSA (Fig. 5B, C) midbrain with and without CIAP pretreatment.Without CIAP, as expected, we observed abundant Lewy pathology (Fig. 5C, left panels) and Papp Lantos bodies (Fig. 5C, right panels) in the PD and MSA brains, respectively.Following CIAP treatment, we observed similar staining in the PD and MSA brains (Fig. 5C, " + CIAP").Image thresholding (Fig. 5D) and quantification confirmed no statistically significant difference in PSER129 staining with or without CIAP pretreatment (Fig. 5E).

Denaturation abolishes aggregated-PSER129 CIAP resistance
αSyn conformational transition to aggregates imparts resistance to proteases.PFF seeded (Figs. 2, 3 and 4) and bona fide αsyn aggregates (Fig. 5A-E) resist CIAPmediated dephosphorylation in situ.To determine if the observed effect was due to the conformation of aggregates, we denatured the brain samples, separated the proteins by WB, and exposed blotted denatured proteins to CIAP.We did this for proteins from untreated WT mice, OB-PFF WT mice, M83 mice, PD midbrain, and MSA midbrain.Results show that in the denatured samples, CIAP abolished PSER129 immunoreactivity in non-aggregate containing samples (i.e., untreated WT) and aggregate-containing samples (i.e., OB-PFF, M83, PD, and MSA) (Fig. 5F).CIAP pretreatment abolished the reactivity of monomeric (14 kDa) and high molecular weight species (> 30 kDa).This shows that conformation imparts resistance to CIAP, analogous to protease-resistance.

Discussion
CIAP pretreatment will help differentiate endogenousvs.aggregated-PSER129 in preclinical animal models.Protease pretreatment (e.g., PK, Trypsin, GluC) could also be used (Additional file 2: Fig. S1), but those treatments are destructive, in particular, PK, and can impede downstream assays (e.g., peptide identification by mass spectrometry, IHC) [20] as well as alter tissue integrity.For this reason, CIAP pretreatment might be a particularly valuable approach to increase specificity for aggregated-PSER129 in multiple assay platforms.Endogenous-PSER129 is CIAP sensitive, and aggregated-PSER129 is CIAP insensitive, this simple observation might help differentiate the two pools in future studies.CIAP-PSER129 may detect early changes in αsyn conformation.CIAP-resistant PSER129 showed high, but not complete, overlap with PK-resistant αsyn (Fig. 4), demonstrating that CIAP-PSER129 was detecting αsyn aggregates and other structures.Some evidence suggests that PSER129 is an early event in the aggregation process [4,34].We speculate that CIAP-PSER129 labeling of the non-dysmorphic neurites of aggregate-containing neurons are early aggregate structures that have not yet become PK resistant.CIAP is a massive protein compared to PK (140 kDa and 28.9 kDa, respectively), and therefore CIAP enzyme may be sterically hindered even for smaller αsyn aggregates that are sensitive to PK.Indeed, disease-causing αsyn mutations impair PSER129 reversibility prior to overt aggregation [6].Therefore, CIAP-PSER129 may be capable of detecting minute abnormal αsyn conformations (i.e., misfolding) prior to larger PK resistant aggregate formation.Future studies are needed to examine this possibility.
Our previous work found widespread regionally specific endogenous-PSER129 in the mammalian brain [7].Here we explain why PSER129 content fluctuated greatly between specimens, with some brain specimens (e.g., rodent and human) showing little or no endogenous-PSER129.We also explain the "all-or-none" effect, where endogenous-PSER129 abundance was proportional across the entire neuroaxis for any rodent brain.Both effects were likely due to differences in the rapidity and completeness of PFA fixation and not because of a global biological process driving endogenous-PSER129 fluctuations in the brain.Rapid (< 5 min) complete perfusion fixation was a critical parameter for preserving endogenous-PSER129, similar to what has been observed with other phosphoepitopes [17].Therefore, studies looking at endogenous PSER129 should ensure proper fixation, and animals where perfusion failed or immersion fixation was used, should be eliminated from analysis.Although not tested here, timely flash freezing or lysis in phosphatase inhibitor buffer can also preserve endogenous-PSER129 [5,16], but investigators should consider any prolonged delay in brain removal, as this may impact endogenous-PSER129 detection.
Our findings suggest an alternative explanation for the long-observed apparent enrichment of PSER129 for αsyn aggregates.Previous studies demonstrated rapid PSER129 dephosphorylation in tissue lysates [2], but here we found endogenous PSER129 (i.e., non-aggregated) is rapidly dephosphorylated intracellularly in the WT mouse brain following death, with PSER129 being undetectable in most brain regions at 1 h PMI.In the human brain, endogenous-PSER129 has only been reported in a single OB (i.e., the structure where endogenous PSER129 is most abundant in rodents and primates) from a patient with a short PMI (~ 2 h).In contrast, endogenous-PSER129 was undetectable in non-synucleinopathy OBs with longer PMIs (> 4 h).Thus, either the human brain is unique from lower mammals (mouse, rat, non-human primate), and endogenous-PSER129 is not abundant, or endogenous-PSER129 in the human brain has evaded detection due to long PMIs common with human donor brain collection.In support of the latter interpretation, CIAP did not significantly affect PSER129 staining in the human brain (Fig. 5A-E), strongly suggesting that these postmortem tissues do not contain endogenous-PSER129.This is consistent with the scenario that aggregated-PSER129 is preferentially preserved during typical postmortem intervals, and apparent PSER129 enrichment in the synuceinopathy brain may result.We established that genuine human αsyn aggregates (Lewy pathology and Papp-Lantos bodies) resist in vitro dephosphorylation.Therefore, PSER129's association with aggregates may result from the dephosphorylation of endogenous-PSER129 and preservation of aggregated-PSER129 during the PMI.Several studies have implicated PSER129 as a mediator of αsyn aggregation [11,14], but our results provide further evidence that, as suggested by others [12,13,35], PSER129 accumulation in the synucleinopathy brain may be an epiphenomenon.Future studies should test this hypothesis, as it will help clarify PSER129's role in synucleinopathies.Furthermore, refining the definition of aggregated-PSER129 (i.e., CIAP resistant) will likely be critical when confirming cases of incidental Lewy pathology based on PSER129 reactivity.These studies have several limitations.First, we cannot conclude a precise mechanism for the observed loss of PSER129 epitope during the postmortem interval, although enzymatic dephosphorylation or proteolysis likely accounts for our observations.Because we did not observe a reduction in total αsyn with postmortem interval (Fig. 1), endogenous phosphatases are likely responsible, but limited C-terminal truncation or ancillary PTMs near the PSER129 epitope is also possible [16].Second, these studies do not provide direct evidence of postmortem dephosphorylation of endogenous-PSER129 in the human brain.This point will be critical to test in future studies to better understand the relationship between PSER129 and synucleinopathy.
Endogenous non-aggregated-PSER129 can be rapidly dephosphorylated and distinguished from aggregated-PSER129 by pretreatment of specimens with CIAP.CIAP pretreatment increases specificity for detecting αsyn aggregates, and thus, CIAP should be used, particularly in preclinical models.This work helps define and differentiate two distinct PSER129 populations (i.e., non-aggregated and aggregated) in the brain.Furthermore, our results support an alternative hypothesis for the long-observed PSER129 enrichment in aggregates of the postmortem synucleinopathy brain.

Tissue preparation and perfusion
Animal tissues were collected by either anesthetizing with ketamine/xylazine (100 mg ketamine/kg and 10 mg xylazine/kg, intraperitoneally), or euthanizing via C0 2 , and then transcrardially perfusing with PBS until the perfusate exiting a small incision in the right atrium was clear.All animals were perfusion fixed, but perfusion fixation was delayed for some animals by clearing blood with PBS and then waiting 30-min (n = 4) or 1-h (n = 4) prior to perfusion with 4% PFA.Rapidly perfused mice (n = 4, "optimal") were quickly flushed with ice-cold PBS (< 30 s) and then immediately perfused with ice-cold 4% PFA.All mice in PFF studies were perfusion-fixed by standard methods [19].Whole brain specimens were removed and post-fixed in 4% PFA at 4 °C overnight.Brains were then equilibrated in 15% and then 30% sucrose solutions.Brain specimens were frozen and sectioned to 40-micron thickness on a freezing stage microtome.Sections were stored in cryoprotectant solution (30% sucrose, 30% ethylene glycol in PBS) at − 20 °C.Perfusion protocol can be found at https:// doi.org/ 10. 17504/ proto cols.io.eq2ly w77pv x9/ v1.

Multiplex tyramide labeling
Detailed multiplex fluorescent tyramide (FT) labeling protocol is available at protocols.io(dx.doi.org/https://doi.org/ 10. 17504/ proto cols.io.yxmvm e7zng 3p/ v1).We specifically adapted this protocol to label CIAP-resistant PSER129 and PK-resistant αsyn simultaneously.To do this, floating sections were first treated with CIAP, as described above.Following CIAP treatment, endogenous peroxidases were quenched and tissues blocked as described above.Tissues were then incubated with EP1536Y (dil.1:50,000) overnight at 4°C.The next day, the sections were washed in DM and then incubated with biotinylated anti-rabbit-igg antibody (Vector Labs) diluted in a blocking buffer for 1 h at room temperature.Sections were washed twice with DM and incubated for 75 min with diluted ABC reagent (Vector labs).Sections were washed twice with DM and then once with borate buffer.Sections were then incubated in freshly prepared FT working solution (Borat buffer, 0.003% hydrogen peroxide, 5 µM CF568) for 30 min at room temperature, protected from light.Sections were then washed twice, and HIAR performed as described above.Sections were then washed in PBS, placed on superfrost plus glass slides, and dried.Slides were then incubated with PK solution (PBS, PK diluted 1:666) for 30 min at 37 °C.The tissues on slides were blocked using Bloxall endogenous blocking solution (Vector Laboratories Cat# SP-6000, RRID:AB_2336257)) for 10 min.After rinsing in DM, the slides were incubated with antibody EPR20535 (Abcam Cat# ab212184, RRID:AB_2941889) (dil.1:20,000) overnight at 4 °C.The following day, the tissues were washed three times in DM and incubated with a biotinylated secondary anti-rabbit antibody (Vector Labs) for an hour, washed in DM, and incubated with prepared diluted ABC reagent (Vector Labs) for 75 min.The tissues were washed in DM three times and incubated with FT working buffer (Borat buffer, 0.003% hydrogen peroxide, 5 µM CF488) for 30 min at room temperature.The tissues were washed in PBS, and counterstained with DAPI (Sigma-Aldrich, 1:2000).Slides were covered with #1.5 glass coverslips using FluoroShield mounting medium (Sigma-Aldrich).Detailed protocol available at protocols.io(https:// doi.org/ 10. 17504/ proto cols.io.x54v9 2dq4l 3e/ v1).

Protein extraction
Proteins were extracted from free-floating PFA fixed tissues sections as previously described [7,36].Briefly, sections were rinsed in DM several times, collected into a 1.5 mL Eppendorf tube, and then heated to 98 °C in reversal buffer (0.5 M Tris-HCl pH 8.0, 5% SDS, 150 mM NaCl, 2 mM EDTA) for 30 min.Samples were vigorously vortexed and heated for an additional 15 min.After cooling to room temperature, samples were centrifuged at 22,000×g for 20 min at room temperature.The supernatant was carefully collected, and a BCA assay was performed on 0.5 µL of extract to determine protein concentration.Detailed protocol available at protocols.io(https:// doi.org/ 10. 17504/ proto cols.io.36wgq 3xyyl k5/ v1).

Microscopy and imaging
Prepared slides were imaged with Nikon A1 inverted microscope using a 10X, 20X or 63X objective.Whole section scans were acquired with either the Nikon A1 microscope with 10X objective, or the Odyssey-M whole slide imaging functionality.Whole section scans were imported into Adobe Photoshop (RRID:SCR_014199) for downsizing, cutting, auto-color balancing, and autobrightness adjustments.Edited images were imported into Adobe Illustrator (RRID:SCR_010279) for arrangement and final presentation in figures.

Quantification of IHC
Brightfield images were captured with an inverted confocal microscope equipped with a 20X objective (Nikon A1R).Annotation of each tissue section was conducted within a bounding box of 2000 × 2000 pixels for mouse tissues and 2863 × 2454 pixels for human tissues.Manual RGB-based color thresholding was used for mouse and for human tissues NIS-elements (version 5.10.01,https:// www.micro scope.healt hcare.nikon.com/ produ cts/ softw are/ nis-eleme nts, RRID:SCR_014329) auto-thresholding algorithm was used.The percentage area of the thresholded signal was exported and normalized to average value of non-CIAP treated tissues.

Fig. 1
Fig.1Experimental conditions required for detection of endogenous-PSER129.Rapid perfusion fixation was required for detection of endogenous-PSER129.Mice were euthanized by CO 2 inhalation, and blood cleared by transcadial perfusion with PBS.Following a delay of 30 or 60 min, mice were then perfused with 4% PFA.A PSER129 staining across the neuroaxis.B High magnification images of PSER129 staining in the hippocampus (HIP) and the OB mitral cell layer (MCL).C Proteins extracted from sections across the neuroaxis were resolved by SDS-PAGE and blotted.Blots were probed for total protein (Revert protein stain, Licor), αsyn, and PSER129.Quantification PSER129 (D) and αsyn (E) per protein normalized to the mean of optimal perfusion control.n = 4. ****ANOVA, Dunnett's post-hoc test.p < 0.0001.Scale bar = 25 µm.Anesthetics did not influence PSER129 abundance in the brain.Mice were euthanized by CO 2 inhalation, and then rapidly fixed by transcadial perfusion with PBS followed by 4% PFA.Ten minutes prior to euthanasia, some animals were exposed to xylazine (XYL, 10 mg/kg) or Ketamine (KET, 100 mg/kg).F PSER129 staining in OB sections.G Proteins extracted from sections across neuroaxis were resolved by SDS-PAGE and blotted.Blots were probed for total protein (G top panel), αsyn, and PSER129.Quantification of total αsyn (H), total PSER129 (I), ratio of PSER129 to αsyn (J), and (K) correlation between αsyn and PSER129 content.No significant differences were found between experimental groups (One-way ANOVA, Tukey's post-hoc).Total asyn did not correlate with total PSER129 (Pearson Correlation, R 2 = 0.01045).All sections developed with nickel-DAB Chromogen (black/purple) and counterstained with methylgreen.n = 4-5

Fig. 2
Fig. 2 Seeded aggregates in WT mice are CIAP resistant.Mice were bilaterally injected with either PBS or PFFs into the OB GCL.Two months following injection, animals were euthanized with a mixture of ketamine/xylazine followed by transcardial perfusion fixation.Brain sections across the neuroaxis were stained for PSER129 with and without CIAP pretreatment.A Whole section images of PSER129 stained brain images across the neuroaxis, with (+CIAP) or without CIAP (−CIAP) pretreatment.B Low and C high magnification images of select brain regions.D Representative images of signal thresholding and E subsequent quantification of PSER129 immunoreactivity in the OB GCL.***Fisher's LSD, p<0.001.**Fisher's LSD, p<0.01.OB olfactory bulb, AMYG amygdala, NaAc nucleus accumbens, HIP Hippocampus, GP Globus pallidus, HYPO hypothalamus, SNPr substantia nigra pars reticulata, MCL mitral cell layer, GCL granule cell layer, EC entorhinal cortex.All sections developed with nickel-DAB Chromogen (black/purple) and counterstained with methylgreen.n = 3. Scale BAR for B = 100 µm, for C = 25 µm, D = 50 µm

Fig. 3
Fig. 3 Seeded aggregates in M83 mice are CIAP resistant.M83 mice were unilaterally injected with αsyn PFFs into the OB GCL. 6 months following injections mice were perfusion fixed.A PSER129 staining in the brain of M83 mouse injected with PFFs without or without CIAP treatment.Red star denotes the OB injected with PFFs.Red line annotates the PA of the PFF injected hemisphere.B High magnification images of CIAP treatment tissue sections from M83 mice injected with either PBS or PFFs.C High magnification images of PA from mouse brain sections treated with CIAP for either 16 h or 70 h.D Representative thresholding of images prior to quantification.E Quantification of PSER129 signal in the OB.****Fisher's LSD, p < 0.0001, n = 3-4.Scale bar for B, C, and D = 50 µm

Fig. 4
Fig. 4 CIAP-resistant PSER129 partially colocalizes with PK-resistant αsyn.Brain sections from M83 mice unilaterally injected with αsyn PFFs into the OB GCL were multiplex labeled for CIAP resistant PSER129 (CIAP-PSER129, red) and PK resistant αsyn (PK-αsyn, green) and nuclei (DAPI, blue).Representative images show labeling in the brainstem (BS) (A), OB and PA (B).Arrows denote the position of cell processes labeled for CIAP-PSER129 but lack overlapping PK-αsyn.C Single plane image of a dysmorphic neurite.D Pearson colocalization coefficients for PK-αsyn and CIAP-PSER129 in the OB and PA.E Plot of pixel intensity values for confocal image of CIAP-PSER129 and PK-αsyn in PA.Pearson correlation coefficient (R) shown on plot.n = 3-4.Scale bars for A = 25 µm, B, C = 20 µm

Fig. 5
Fig. 5 Human brain αsyn pathology is phosphatase resistant.Whole section images of transverse midbrain sections from A PD and B MSA cases stained for PSER129 with (+CIAP) or without CIAP pretreatment.High magnification images of substantia nigra of C PD and MSA.D Representative thresholding of images prior to quantification.E Quantification of staining in PD and MSA brain with or without CIAP.F Proteins extracted from tissues that either did or did not have αsyn aggregates.Proteins were separated by SDS-PAGE and blotted onto PVDF membranes which were incubated with and without CIAP.Blots were probed for both PSER129 and αsyn.All sections developed with nickel-DAB Chromogen (black/purple) and counterstained with methylgreen n = 5-10.Scale bars for A and B = 2 mm, for C = 25 µm, for D = 150 µm.ns = non-significant