- Open Access
Dysregulation of lysophosphatidic acids in multiple sclerosis and autoimmune encephalomyelitis
- K. Schmitz†1,
- R. Brunkhorst†2,
- N. de Bruin3,
- C. A. Mayer2,
- A. Häussler1,
- N. Ferreiros1,
- S. Schiffmann3,
- M. J. Parnham3,
- S. Tunaru5,
- J. Chun6,
- S. Offermanns5,
- C. Foerch2,
- K. Scholich1,
- J. Vogt4,
- S. Wicker7,
- J. Lötsch1, 3,
- G. Geisslinger1, 3 and
- I. Tegeder1, 8Email authorView ORCID ID profile
© The Author(s). 2017
Received: 2 May 2017
Accepted: 21 May 2017
Published: 2 June 2017
Bioactive lipids contribute to the pathophysiology of multiple sclerosis. Here, we show that lysophosphatidic acids (LPAs) are dysregulated in multiple sclerosis (MS) and are functionally relevant in this disease. LPAs and autotaxin, the major enzyme producing extracellular LPAs, were analyzed in serum and cerebrospinal fluid in a cross-sectional population of MS patients and were compared with respective data from mice in the experimental autoimmune encephalomyelitis (EAE) model, spontaneous EAE in TCR1640 mice, and EAE in Lpar2 -/- mice. Serum LPAs were reduced in MS and EAE whereas spinal cord LPAs in TCR1640 mice increased during the ‘symptom-free’ intervals, i.e. on resolution of inflammation during recovery hence possibly pointing to positive effects of brain LPAs during remyelination as suggested in previous studies. Peripheral LPAs mildly re-raised during relapses but further dropped in refractory relapses. The peripheral loss led to a redistribution of immune cells from the spleen to the spinal cord, suggesting defects of lymphocyte homing. In support, LPAR2 positive T-cells were reduced in EAE and the disease was intensified in Lpar2 deficient mice. Further, treatment with an LPAR2 agonist reduced clinical signs of relapsing-remitting EAE suggesting that the LPAR2 agonist partially compensated the endogenous loss of LPAs and implicating LPA signaling as a novel treatment approach.
One sentence summary
Lysophosphatidic acids are reduced in patients with multiple sclerosis and in EAE mice, and the consequent loss of LPAR2 signaling in immune cells promotes the disease.
Lysophosphatidic acids (LPAs) are lipid-signaling molecules of different chain lengths and phosphorylation. Presently, 6 different LPAs can be detected in biological fluids or tissue extracts  and they signal through specific, functionally diverse G-protein coupled LPA receptors, LPAR1-5, and the atypical LPAR6 [6, 33]. LPARs are differentially expressed by various kinds of immune cells and may preferentially engage saturated or mono/poly unsaturated LPAs . Signal transduction through LPARs regulates cell mobility and migration [25, 71], neuro - and angiogenesis , and platelet aggregation . Their functions in the context of multiple sclerosis (MS) are presently unknown.
The discovery of the mechanisms for extracellular LPA generation has stimulated research of their function for innate and adaptive immunity and immune cell signaling. There are two major pathways for extracellular LPA production : (i) by direct hydrolysis of a fatty acid moiety from membrane-derived phosphatidic acid  and (ii) by removal of the choline moiety from the abundant lysophosphatidylcholine (LPC) [56, 60]. The latter process is mediated by autotaxin (ATX), a secreted lysophospholipase D (lyso-PLD), which is a multidomain and multi-functional protein, with lyso-PLD and phosphodiesterase enzyme activities [40, 56, 67].
ATX is normally expressed by high endothelial cells of lymph node venules i.e. at the sites of immune cell transmigration . It is also expressed by oligodendrocyte precursor cells  and activated astrocytes , and promotes the morphological maturation of glial cells  and myelination . On stimulation, autotaxin binds to integrin of cell surfaces via its somatomedin-B like domain [21, 26], then utilizes LPC of the target cell membrane to produce LPAs in the close vicinity of the targeted LPA receptor, a mechanism that confers specificity. The ATX-mediated targeted release of LPAs may orchestrate LPA-effects in lymphoid organs and at the blood brain barrier and hence immune cell adhesion, invasion into or evasion from the brain .
Studies with small molecular autotaxin inhibitors have suggested that LPAs have pro-inflammatory functions [29, 50], but the outcome depends on the where and when of their production, the target receptor [44, 72], and the ability to maintain a balance between production and breakdown, the latter mediated by membrane bound lipid phosphate phosphatases (LPPs) . The sphingsosine 1-phosphate (S1P) receptor antagonist fingolimod, which is one of the most effective relapse preventing drugs in relapsing remitting multiple sclerosis (RRMS) , has been reported to also be a slow acting autotaxin inhibitor  and protects against deregulation of signaling lipids at the blood brain barrier . It is unknown to what extent this effect contributes to, or interferes with its efficacy in MS.
To gain further insight into the functions of the ATX/LPA axis for neuroimmunological diseases we used a translational approach. We analyzed LPAs and autotaxin in a cross sectional population of MS patients and in mice in the experimental autoimmune encephalomyelitis model (EAE), using immunization-evoked primary progressive and relapsing-remitting EAE, spontaneous EAE, and EAE in Lpar2 deficient mice, the latter to assess functional implications of LPA signaling and LPAR-dependent immune cell redistribution. Finally, we assessed the therapeutic effects of an LPAR2 agonist.
Materials and methods
Patients with multiple sclerosis
Demographic data of Multiple sclerosis patients and healthy control subjects
Multiple sclerosis patients
MS 1st course
RRMS acute relapse
SPMS or PPMS
MS 1st course
RRMS acute relapse
SPMS or PPMS
Total number (m/f)
Number (all treatments)
Age (Years mean ± SD)
38.2 ± 7.5
35.5 ± 0.4
33.9 ± 7.0
43.6 ± 18.1
31.6 ± 9.1
34.3 ± 8.9
37.2 ± 10.9
49.3 ± 11.0
35.5 ± 9.7
25.0 ± 6.1
24.9 ± 6.1
25.0 ± 6.1
Years since diagnosis
0.1 ± 0.4
7.6 ± 6.1
2.1 ± 1.8
5.7 ± 4.7
0.8 ± 0.2
7.4 ± 5.9
6.7 ± 5.3
1.1 ± 1.3
5.6 ± 5.7
Relapse prophylaxis Number of patients
Animals, drug treatments and kinetics
Female SJL/J mice (Envigo, Germany), aged 10–12 weeks at immunization were used for study of relapsing-remitting EAE and female TCR1640 mice for spontaneous RR-EAE . Female C57BL6/J mice and LPAR2−/− mice and LPAR2+/+ littermates were used for the study of primary progressive EAE. LPAR2−/− mice have a mixed C57BL6/J x Sv129 background with about 25% Sv129. Mice were housed at 3–5 mice per cage at constant room temperature (21 ± 1 °C) under a regular 12 h light/dark schedule. Food and water were available ad libitum. Animals were treated orally via the drinking water with FTY720 (fingolimod) at 0.5 mg/kg/d starting 3 days after immunization for preventive treatment. Monoclonal anti-Itga4 antibody treatment (natalizumab) in SJL/J mice consisted in 3 intraperitoneal injections (1x200 μg, 2x 150 μg) on day 11, 14 and 19. The LPAR2 agonist GRI 977143 was administered perorally in cornflakes soaked with 10% sucrose/10% DMSO in water with 100 μg/mouse/d of the drug starting 3d after immunization. Control animals received the respective vehicle. Oral bioavailability (F) of the LPAR2 agonist and basic kinetics were assessed by LC-MS/MS analysis of plasma concentrations. Tmax and Cmax were directly taken from the plasma concentration time courses. AUCs were calculated according to the linear trapezoidal rule. The clearance was calculated as Cl = Dose*F/AUCs and the half-life, t1/2 = ln2/λ, where λ is the terminal decay constant.
The experiments adhered to the guidelines of the Committee for Research and Ethical Issues of the International Association for the Study of Pain (IASP) and to those of GV-SOLAS for animal welfare in science and the ARRIVE guidelines. They were approved by the local Ethics Committee for Animal Research (Darmstadt, Germany).
C57BL6/J and LPAR2 mice were immunized according to a standard protocol using the Hooke Kit™ MOG35-55/CFA emulsion PTX (EK-2110, Hooke Labs, St Lawrence, MA), which contains 200 μg myelin oligodendrocyte glycoprotein (MOG) 35–55 emulsified in 200 μl Complete Freund’s Adjuvant (CFA). The emulsion was injected subcutaneously at two sites followed by two intraperitoneal (i.p.) injections of 200 ng pertussis toxin (PTX) in phosphate buffered saline (PBS), the first 1–2 h after MOG35-55, and the second 24 h later. SJL mice were immunized using Hooke Kit™ PLP139-151/CFA emulsion PTX (EK-2120), which contains 200 μg myelin proteolipid protein (PLP) 139–151 in 200 μl CFA (Hooke Labs, US). Injections of the emulsion and PTX were done as described for C57BL6 mice.
TCR1640 transgenic mice carrying a T-cell receptor (TCR) specific for myelin oligodendrocyte glycoprotein (MOG) peptide 92–106 develop spontaneous EAE around the age of 3 months . TCR1640 positive male mice were mated with wild type female SJL/J mice. TCR1640 positive litter were identified by FACS analysis of peripheral blood T-cells by identification of the TCRα8.3 and TCR-β4 chains using specific antibodies for Vα8.3 (B21.14) and Vβ4 (KT4) (Becton Dickinson) . Female TCR1640 positive mice were observed for up to 6 months.
EAE scores were assessed daily to evaluate the severity and extent of motor function deficits. Score 0, normal motor functions; score 0.5, distal paralysis of the tail; score 1, complete tail paralysis; score 1.5, mild paresis of one or both hind legs; score 2, severe paresis of hind legs; score 2.5, complete paralysis of one hind leg; score 3, complete paralysis of both hind legs; score 3.5, complete paralysis of hind legs and paresis of one front leg. Serum and tissues were sampled after the second peak, 35–36 days after immunization.
Blood was sampled by puncture of the retrobulbar plexus or by cardiac puncture (final sample) into EDTA K+ microvettes for plasma or microvette® 200 Z-gel (Sarstedt) for serum samples. Blood was centrifuged at 3000 rpm for 10 min in a table centrifuge and plasma or serum samples were stored in standard Eppendorf caps at −80 °C until analysis. Tissue from specific brain regions and spinal cord and peripheral tissues (spleen, lymph nodes) were rapidly dissected and snap frozen on dry ice and stored at −80 °C.
Analysis of lysophosphatidic acids
Quantitative LPA analysis was performed with liquid chromatography-electrospray ionization-tandem mass spectrometry (LC-ESI-MS/MS) with a hybrid triple quadrupole-ion trap QTrap 5500 mass spectrometer (AB Sciex, Germany) as described [63, 73] without knowledge of clinical data or treatment groups. Briefly, 2 cycles of liquid-liquid extraction of LPAs were done with 1-buthanol after adding the internal standard LPA17:0 (50 μl sample, 20 μl internal standard in 500 μl 1-butanol). The combined organic phases were dried under a gentle stream of nitrogen at 45 °C and subsequently re-dissolved in 200 μl methanol. A C18 column (Mercury 20 x 2 mm, 3 μm, 100 Å) and precolumn were used for chromatographic separation. A linear gradient was employed at a flow rate of 400 μl/min. Mobile phase A was water with ammonium formate 50 mM and formic acid (100:0.2, v/v) and mobile phase B acetonitrile/formic acid (100:0.1, v/v). The mass spectrometer operated in the negative ion mode and used multiple reaction monitoring (MRM). The mass transitions were m/z 409 → 79 (LPA 16:0), m/z 437 → 153 (LPA 18:0), m/z 431 → 79 (LPA 18:3) and m/z 457 → 153 (LPA 20:4) all with a dwell time of 50 ms. The internal standard method was used for quantification with Analyst Software V1.5 (Applied Biosystems, Germany). The calibration curve was linear over the range of 0.1–500 ng/ml and accuracy was >95%.
Primary cell culture
The spleens were removed and collected in a sterile wire mesh with 40 μm pore size over a Petri dish half filled with RPMI 1640 media and were gently pressed through the mesh using a 5 ml syringe plunger. The mesh was rinsed over the Petri dish with additional media to remove remaining cells. Disaggregated cells were transferred to a 15 ml Falcon tube and centrifuged at 2,000 rpm for 5 min and washed 2x in RPMI. The cell pellet was resuspended in RPMI, treated with erythrocyte lysis buffer for 10 min at room temperature, followed by centrifugation and resuspension in full medium (RPMI 1640 + 10% FBS + 1% Pen/Strep). Cells were plated in 6-well plates at 3x106/2 ml per well. Growth was stimulated with concanavalin A at 1 μg/ml. Cells were kept in an incubator at 37 °C, 95% humidity and 5% CO2 atmosphere and assays were performed after 2d in culture.
Enzyme immune assay of autotaxin
Serum samples or crude protein extracts were mixed with a protease inhibitor cocktail (Roche) and subsequently snap frozen in liquid nitrogen and stored at −80 °C until analysis. Proteins from tissue homogenates and primary cells were extracted in PhosphoSafe Buffer (Sigma Germany) containing a protease inhibitor cocktail (Roche) and PMSF 10 μg/ml. The autotaxin ELISAs were used according to the instructions of the manufacturers (R&D systems for human; MyBioScource for mouse). Samples were diluted 1:2 or 1:10, and 50 μl were subjected to the ELISA. Results in tissue are normalized to mg of protein, which was determined with the Bradford assay.
The lyso-PLD activity of ATX was measured in primary splenocytes of naïve and EAE mice. Cells were incubated for 2 h in 1.1 ml serum free RPMI 1640 medium and then stimulated for another 2 h with PMA 50 ng/ml and ionomycin 500 ng/ml in serum free medium before the autotaxin substrate, C17-LPC was added (100 μM in 1 μl in DMSO). Cell culture supernatants were harvested before adding C17-LPC (baseline) and at 0.5, 1 and 2 h (each sample 100 μl) and cell pellets were collected at 2 h. C17-LPC is converted into the unnatural C17:0-LPA, which was analysed in supernatants and crude cell extracts by LC-MS/MS as described above. LPA18:3 was used as internal standard.
LPA receptor activation with different LPAs
To study the activation profile of heterologously expressed LPA receptors, COS-1 cells were seeded in 96-well plates at a density of 50.000 cells/well. Next day, they were co-transfected with plasmids containing cDNA for a calcium-sensitive bioluminescent fusion protein between aequorin and GFP  and plasmids containing the indicated receptor cDNA or control (empty vector, mock) together with the promiscuous Gα15  at a concentration of 50 ng/well by using FuGENE 6 reagent (Promega) according to manufacturer’s instructions. Forty-eight hours later, cells were loaded with 5 μM coelenterazine h (Invitrogen) in HBSS buffer containing 1.8 mM CaCl2 and 10 mM glucose for 2 h at 37 °C. Measurements were performed by using a luminometric plate reader (Flexstation 3) for 100 s following ligand stimulation. The area under each calcium transient was calculated by using SoftMaxPro software and expressed as area under the curve (AUC). The following lipids were used for stimulation: 1-Palmitoyl-LPA (LPA16:0), 1-oleoyl-LPA (LPA18:1), 1-stearoyl-LPA (LPA18:0), 1-lineoyl-LPA (LPA18:2), 1-arachidonoyl-LPA (LPA20:4). LPA16:0 and 18:1 were from Cayman, the others from AvantiPolar Lipids.
Single cell suspensions were prepared from the spleen, lymph nodes and the lumbar spinal cord. Tissues were rapidly dissected, treated with lysis buffer (DMEM/Accutase (PAA) 1:1, collagenase (3 mg/ml, Sigma), DNAse I (1U/ml, Promega)) for 45 min at 37 °C and followed by mechanical disruption, which was done by forcing the tissue through a nylon mesh with 70 μm pore size (Cell Strainer, BD). For FACS analysis of circulating cells, K+ EDTA blood was used. Blood samples or cell suspensions (100 μl) were mixed with 100 μl HEPES buffer (20 mM HEPES) and 1 ml erythrocyte lysis buffer for 10 min at room temperature and CD16/32 blocking antibody (Fcγ RII/III receptor blocker, BD) for 15 min on ice. Cells were incubated for 20 min at room temperature in staining buffer with the respective fluorochrome labeled antibodies (Additional file 1: Table S1) and were then counted with a flow cytometer (BD FACS Canto II). FACS scans were analyzed with FlowJo 10.08. The controls were FITC, PE, or APC-conjugated rat IgG.
Quantitative RT-PCR analysis of LPA receptors
Total RNA was extracted from homogenized tissue according to the protocol provided in the RNAeasy tissue Mini Kit (Qiagen, Hilden, Germany), and reverse transcribed using poly-dT as a primer to obtain cDNA fragments. QRT-PCR was performed on an ABI prism 7700 TaqMan thermal cycler (Applied Biosystems, Germany) using the SybrGreen detection system with primer sets and probes designed on the TaqMan software (Additional file 2: Table S2). Amplification was achieved at 59 °C for 40 cycles and confirmed with gel electrophoresis. Transcript regulation relative to the housekeeping gene, Gapdh was determined using the relative standard curve method according to the manufacturer’s instructions (Applied Biosystems).
Immunofluorescence analysis of immune cell infiltrates in the spinal cord
Mice were terminally anaesthetized with isoflurane and cardially perfused with cold 0.9% NaCl, followed by 4% paraformaldehyde (PFA) in 1x PBS for fixation. Spinal cord and brain were excised, postfixed in 4% PFA for 2 h, cryoprotected overnight in 20% sucrose at 4 °C, embedded in tissue molds in cryomedium and cut on a cryotome (12 μm). Immunofluorescent stainings were done as described  (antibodies in Additional file 1: Table S1).
Tiled images of individual sections were captured with equal filter and acquisition parameters to assure comparability independent of genotype or treatment and subsequently stitched to cover the complete ventral horn of the spinal cord. Iba1+ and CD11b + microglia/macrophages in the gray matter and white matter were quantified using the particle counter plugin of FIJI ImageJ. After 8bit conversion, the background was subtracted and the intensity threshold set using the IJ_IsoData algorithm implemented in FIJI. For the particle counter, size inclusions were set to 5–575 μm2. Average particles sizes were 20 μm2 and 28 μm2 for Iba1+ and CD11b + particles, respectively. Three or more non-overlapping images of 3 mice were analyzed per group.
Data are presented as scatter plots with mean ± standard deviation or box plots where the box is the interquartile range and the whiskers show minimum and maximum. Data were analyzed with SPSS 23 and GraphPad Prism 6.0. LPA concentrations were compared between groups using analyses of variance (ANOVA), t-tests or Mann-Whitney U tests according to the data structure and distribution. Trends were analyzed using the Jonckheere-Terpstra trend test. Further analyses consisted of correlation (Spearman’s ρ) and χ2 statistics. To assess differences of all LPAs simultaneously, total concentrations were transformed to z-scores according to the equation z = X - μ/σ, where X is the individual value, μ the mean and σ the standard deviation, followed by two-way ANOVA with the within subject factor “LPA” and the between subjects factor “group”, i.e. healthy versus MS in patients and naïve, EAE, EAE-fingolimod, EAE-NTZ in mice. Time courses for LPAs were submitted to analysis of variance for repeated measurements (rm-ANOVA). The within subject factor was ‘time’. Gender was introduced as a between-subject factor and age as covariate. In the case of significant results in the ANOVA, groups were mutually compared with t-tests. The alpha level was set at 0.05 for all comparisons and corrected for multiple testing according to the procedures of Dunnett or Bonferroni.
Reduction of serum LPAs in MS patients and EAE mice
Concentrations of LPAs with different chain lengths and phosphorylation (LPA16:0, 18:0, 18:2, 18:3 and 20:4) were obtained in the serum of 102 MS patients and 301 healthy controls with equal distribution of sexes (χ2 test: p = 0.410). All LPAs were significantly reduced in MS patients (two tailed, unpaired Student’s t-tests P < 0.0001 for each LPA; Fig. 1a). Similar results were obtained with two-way ANOVA using “LPA” by “group” (for “group”: F (1, 356) = 81.83, P < 0.0001; for the interaction “LPA x group” F (5, 1780) = 58.23; P < 0.0001) and subsequent Bonferroni posthoc analyses. As healthy subjects were younger than MS patients (Demographic Table 1) the analysis was repeated for subsets of gender and age matched patients and controls > 30 years. The subgroups encompassed 65 MS patients and 36 controls aged 41.0 ± 7.6 and 38.5 ± 7.7 years, respectively (t-test for age: p = 0.119). Still, all LPAs were significantly reduced in MS patients (LPA16:0 P = 0.015, 18:0 P = 0.020, 18:1 P <0.0001, 18:2 P = 0.002, 18:3 P = 0.003, 20:4 P < 0.0001). Linear regression analyses did not show a significant association of the sum of all LPAs with age or body mass index (BMI) in healthy controls (correlation coefficients for age: -3.643, P = 0.141, BMI −6.680, P = 0.181) or age in MS patients (R2 = 2.435, P = 0.115). BMI data of MS patients were not available.
The LPA pattern of MS patients was compared with that of SJL/J mice in the EAE model of multiple sclerosis (Fig. 1b). Blood was sampled during the second interval 35 days after immunization, where no signs of the disease were detectable. This agrees with majority of patients who mostly had a stable RRMS. Similar to MS patients, EAE mice had significantly reduced LPA serum concentrations compared with control SJL/J mice (2-way ANOVA for “group” F (1, 18) = 7.412, P = 0.0140, for interaction “group x LPA” F (5, 90) = 4.667, P = 0.0008).
LPAR preferences of different LPAs
Relapse associated LPA changes in MS patients and spontaneous EAE
To further assess the effect of relapse and medication in MS patients we analyzed time courses of LPAs in a subset of MS patients over a period of several months to years (Fig. 2). The patients participated in clinical efficacy studies of fingolimod (FTY720) or natalizumab (NTZ). Regulations of LPAs were again congruent. The concentrations of the unsaturated LPAs, LPA18:1, 18:2 and 20:4, i.e. the receptor-activating LPAs, (Fig. 1d) were averaged to show the individual time courses. The patients clustered in two groups: in the first, clinical relapses were associated with elevated LPA concentrations, whereas in the second group the opposite was true, i.e. LPAs were particularly low during relapses, which were in part refractory relapses.
The highly variable course of the disease in MS patients is not well mimicked by the immunization-induced EAE model. Therefore, we used the spontaneous EAE model in TCR1640 transgenic mice, which spontaneously develop a T- and B-cell dependent EAE to monitor and compare stage-associated LPA alterations in plasma and spinal cord tissue. The time courses of the clinical scores mimic the highly variable human disease (Fig. 2 bottom). We observed a mild increase in plasma LPAs during the first peak and a stronger increase in the first interval that was followed by a decrease in the late stage of the disease (Fig. 2b), the latter similar to the situation in patients. We used plasma instead of serum for this experiment to exclude the impact of platelets. LPA concentrations in plasma are about 5–10 fold lower than in serum. The increase during the 1st interval was associated with a stage-dependent increase in the lumbar spinal cord (Fig. 2c) i.e. in a ‘symptom-free’ period reflecting the resolution of inflammation.
Effects of treatments on LPA changes
Patients with RRMS normally receive prophylactic treatment to reduce the frequency and number of relapses. Two of the latest available drugs are the sphingosine-1-phosphate analog, fingolimod and the alpha-4 integrin (VLA4) targeting monoclonal antibody, natalizumab. To assess the effect of treatment we compared serum LPAs in medication-subgroups in MS patients and EAE mice and the clinical EAE courses in SJL/J mice receiving these treatments (Fig. 3). LPA concentrations in serum of patients treated with fingolimod or natalizumab were significantly lower than in patients not receiving medication, or receiving beta interferon or other drugs including glatiramer, azathioprine, repeated glucocorticoid cycles or fumarate (two-way ANOVA for factor ‘medication’ F (4, 103) = 3.012468, P = 0.0214 and ‘medication x LPA’ F (20, 515) = 2.267692, P = 0.0014; posthoc Dunnett results in Fig. 3a, b). The additional LPA lowering effect was also observed in fingolimod or natalizumab treated EAE mice (Fig. 3c–e). Comparison of EAE versus EAE & Fingolimod was highly significant for LPA18:2 and the sum of all LPAs (one-way ANOVA F (2, 22) = 7.995962, P = 0.0025, posthoc in Fig. 3d), but the trend was also visible for LPA16:0, 18:1, 18:3 and 20:4 (Jonckheere’s trend tests for these LPAs all P < 0.001). Similarly, natalizumab treated mice had significantly lower LPA levels than vehicle treated mice (Fig. 3e). We used NTZ although it has been raised against human Itga4, which has 85% identity with mouse Itga4. NTZ treatment in SJL/J mice, consisting in 3 injections at d11, 14, 19, reduced the clinical scores whereas fingolimod, which is highly active in C57BL6 mice, had only minor effects in SJL/J mice as shown before  (Fig. 3 f, g).
LPAs and autotaxin in ICD10 subgroups of patients
We compared levels of LPAs in disease subgroups according to the clinical ICD10 score (Fig. 4a). In all MS subgroups, serum LPA levels were significantly lower than in healthy controls and subgroups were similar, but patients with acute relapse tended to have higher levels (n.s.) than the other patient groups, which is in line with the individual time courses of patients in cluster-1 (Fig. 2). Extracellular LPAs are mainly produced by autotaxin and we found a linear association of LPAs with autotaxin concentrations both in healthy subjects and MS patients (Fig. 4b). However, ICD10 subgroup associations with serum autotaxin were rather inverse to those of LPAs (Fig. 4c). In RR-EAE, serum autotaxin levels were unaltered during the ‘symptom-free’ second interval (Fig. 4d) but autotaxin levels were increased in the spleen, possibly reflecting local upregulation. Ex vivo, ATX activity in primary splenocytes was similar in control and EAE mice (Fig. 4e), but the maximum stimulation effect of PMA/Ionomycin was significantly reduced in splenocytes from natalizumab treated mice (Fig. 4e). Inhibition of ATX with PF8380 mainly reduced unsaturated LPAs in plasma in naïve mice (Fig. 4 f), again suggesting that saturated and unsaturated LPAs were differentially regulated.
LPA receptor subtypes in immune cells
EAE in LPAR2 deficient mice and therapeutic effects of LPAR2 agonist
The present study revealed a deficit of extracellular peripheral LPAs in MS patients and in EAE mice, whereas spinal cord LPAs increased during the remyelination phase in EAE. The apparent peripheral LPA deficiency was associated with impaired homing of LPAR2+ T-cells to the spleen and intensified clinical signs of EAE in LPAR2−/− mice. Conversely, mice treated with an LPAR2 agonist were partially protected from the disease. Together these loss- and gain-of-function experiments suggest that LPAs have protective functions in MS and EAE (i) by increasing lymphocyte homing and (ii) possibly, by promoting remyelination. The latter idea is suggested by previous studies showing that LPAR1 is highly expressed by oligodendrocytes  and essentially contributes to myelination , Schwann cell migration  and proper cortical development [17, 20]. Hence, individual time courses of LPAs may point to changes in disease activity.
It is presently not clear whether different LPAs have specific functions, prefer specific LPARs or are preferentially produced by autotaxin or phospholipase A in the settings examined here. Mostly, we found congruent regulations of all LPAs with linear relationships between LPAs, but the in vitro studies in COS cells suggest that unsaturated LPAs are the major LPAR activators. Indeed, the disease-course associated fluctuations of the unsaturated LPAs matched the individual activity of the disease, were affected by natalizumab and fingolimod, and were exclusively reduced by autotaxin inhibition. While our data mainly suggest protective functions, LPAs may also trigger pro-inflammatory cellular responses [39, 41], depending on the receptor and the source. For example, platelet-derived LPAs trigger the degranulation of neutrophils  that contribute to MS pathology  and a recent study observed a reduction of EAE manifestations with an autotaxin inhibitor that blocks its catalytic phosphodiesterase activity . The individual LPA time courses of our patients did not give a clear answer, because patients clustered in 2 groups, one with high levels of LPAs during relapse, the other with particularly low levels, which were in part refractory relapses non-responding to treatments. Glucocorticoids, which are frequently administered during relapses may interfere with the ‘natural’ LPA course, because they may inhibit autotaxin  and sPLA2 , the latter actually being unfavorable for the immune regulatory functions of regulatory T-cells (T-regs) . The observed regulation of autotaxin points to a functional dichotomy but the functions of ATX for myelination [14, 19], although likely mediated by its MORPHO domain and not affected by inhibitors of its phosphodiesterase activity, rather discourages targeting ATX for treatment of MS, supported by our data.
The MS- and EAE-associated reductions of LPAs were further intensified under treatment with fingolimod and natalizumab, affecting mainly unsaturated LPAs. Notably, these effects were seen in MS patients and in the EAE model arguing for genuine effects of natalizumab and fingolimod rather than putative effects caused by higher disease-activity, which is important because fingolimod and natalizumab are highly potent agents restricted to an escalation medication. The effect of fingolimod may be due to autotaxin inhibition . The effects of natalizumab are possibly due to interference with the binding of autotaxin to integrin, which is required for targeting the enzyme to cell surfaces to get access to its substrate, phosphatidylcholine (LPC) , and indeed, the maximum stimulated activity of autotaxin was reduced in splenocytes of natalizumab-treated EAE mice. We used natalizumab in the EAE experiments to match the human data. NTZ was raised against human Itga4, which is 85% identical with the mouse protein, and binds human and mouse Itga4 differently  but prevents T-cell BBB penetration in EAE mice in vivo  and effectively reduced the EAE scores in our mice.
In spontaneous EAE mice, the peripheral LPA loss occurred during a late stage of the disease like in the majority of patients whereas the ‘symptom-free’ interval was associated with LPA increases in the lumbar spinal cord. Hence, the central LPA peak paralleled the resolution of inflammation and time of remyelination. One may interpret this local increase as a sign of protective central effects of LPAs through their receptors on myelinating cells [1, 23, 66] as well as neural stem cells [28, 34, 65, 66]. Consistently, autotaxin is increasingly released at the onset of myelination  and maintains functions of oligodendrocytes , and secreted PLA2 (sPLA2), which is an extracellular source of LPAs, protects oligodendrocytes from cell death , further consistent with LPA’s survival effects on Schwann cells . MS and EAE evoked reductions of LPAs therefore suggest unfavorable adaptations, and medication-evoked further reductions may be side effects compromising LPA-regulated immune cell traffic, but this apparently does not curtail the proven efficacy of fingolimod or natalizumab in human MS [9, 27] but possibly may increase the risk of side effects.
Fingolimod is supposed to act through a retention of immune cells in the lymphoid organs suggesting that bioactive lipids are key regulators of the interplay of homing and egress . The entry of naive lymphocytes into the lymph nodes occurs at high endothelial venules, requiring attachment and extravasation into the tissue [15, 32]. Although the exact mechanisms of LPA mediated transmigrations are under debate [32, 38] it is conceivable that a permanent reduction of LPAs interferes with the migrating properties [2, 70]. It is presently unknown whether LPAs act on T-cells, endothelial cells, or both, and different models have been proposed. Locally generated LPAs may facilitate T-cell exit from the circulation and entry into lymph nodes via T-cell LPARs , mainly LPAR2 and LPAR5 . The ATX/LPA signaling may also regulate T-cell homing indirectly by acting on LPARs of endothelial cells , which express LPAR1 and LPAR4 . In addition, LPAs modify the cytoskeleton of the endothelial cells necessary to modify their shape and motility, and ATX inhibitors can block lymphocyte extravasation [2, 32]. Regardless of the exact mechanisms involved, the possibility that LPAs promotes T-cell homing and recirculation through lymphoid organs is an exciting new direction and complements the well-recognized role of sphingosine 1-phosphate (S1P) in lymphocyte egress . Hence, LPAs and S1P may act as functional antagonists in this process. The observed decrease of LPAR2 positive T-cells and myeloid cells in the spleen, increase of its mRNA in circulating WBCs and in the lumbar spinal cord, strongly suggest that LPAR2 is one of the crucial receptors. In line with this idea, LPAR2 deficient mice developed stronger EAE than controls and treatment with the LPAR2 agonist reduced clinical signs of EAE, albeit with high variability. In addition to immune effects, both LPA and S1P receptors are widely expressed in the CNS where they are likely to have a range of direct CNS activities relevant to both EAE and MS, as demonstrated by a requirement for astrocyte S1P1 for fingolimod activity in EAE [5, 24] and LPAR1 for myelination . Moreover, promiscuity of lipid ligands as shown by endocannabinoid metabolites acting through LPA receptors  adds further potential to explain variation. Cell-type specific LPAR-deficient mice will help to dissect out specific LPAR functions in the future, and possibly dual agonists may have less variable efficacy.
In summary, we show a reduction of LPAs in serum in patients with multiple sclerosis, individual relapse dependent re-raises or further downregulations, and further reductions under treatment with fingolimod and natalizumab. The alterations are also evident in mice with relapsing-remitting EAE and spontaneous EAE and the LPA loss was associated with reduced lymphocyte homing of LPAR2 positive T-cells. Finally, complete deficiency of LPAR2 aggravated EAE whereas an LPAR2-agonist treatment attenuated the disease. Together, the data suggest that functional deficits of LPA-LPAR2 signaling contribute to the pathophysiology of multiple sclerosis and possibly might be targeted by specific treatments.
We thank Sandra Labocha for technical assistance and Prof. Hartmut Wekerle (Max Planck Institute, Munich, Germany) for providing TCR1640 mice.
This work was financially supported by the Deutsche Forschungsgemeinschaft (CRC1039 A03, A04, A08, Z01 and CRC1080 B05, A03), the Else Kröner Fresenius Foundation (Translational Research Innovation Pharma (TRIP) graduate school, I.T.) and the Landesoffensive für Wissenschaftliche und Ökonomische Exzellenz (LOEWE) Research Center for Translational Medicine and Pharmacology of the State of Hessen. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Conceived and designed the experiments: IT. Performed the experiments: RB, KS, AH, CAM, NdB, NF, ST. Analyzed data: KS, KScho, ST, NF, NdB, JL, IT. Contributed data, clinical samples or other materials: SS, RB, CAM, CF, JC, SW, MP, JV, SO, GG. Wrote the paper and created the figures: IT. Drafting or critically revising parts of the manuscript: all authors. All authors read and approved the final manuscript.
The authors declare that they have no competing interests.
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