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Reduced expression of somatostatin in GABAergic interneurons derived from induced pluripotent stem cells of patients with parkin mutations
Molecular Brain volume 12, Article number: 5 (2019)
Parkinson’s disease (PD) is associated with both motor and non-motor symptoms, including constipation, sensory neuropathy, depression, dementia and sleep disorder. Somatostatin (SST) is considered to be a modulator of GABAergic inhibitory transmission, and its levels are reduced in cerebrospinal fluid of PD patients. In the present study, we evaluated the changes in the expression of SST in GABAergic neurons derived from induced pluripotent stem cells (iPSCs) of PD patients. Neural cells were co-treated with the Wnt antagonist IWP-2 and Shh during neurosphere formation to induce GABA-positive forebrain interneurons. Quantitative analyses showed no significant differences, but slight decreases, in the potency of differentiation into GABAergic neurons derived from iPSCs between healthy control and patients with PARK2 mutations, who have been classified as a type of early-onset familial PD due to mutations in the parkin gene. Under this condition, the mRNA level of SST in GABAergic interneurons derived from iPSCs of PARK2-specific PD patients significantly decreased as neural maturation progressed. We also found that SST-positive GABAergic neurons were clearly reduced in GABAergic neurons derived from iPSCs of patients with PARK2 mutations. These findings suggest that the reduction in the expression level of SST in GABAergic interneurons of PD may, at least partly, lead to complex PD-induced symptoms.
Parkinson’s disease (PD) is a progressive neurodegenerative disorder that afflicts about 4,000,000 patients worldwide . While PD symptoms are mainly due to the progressive degeneration of neuronal cells in the substantia nigra , various other types of neural cells in the central and peripheral autonomic nervous systems also contribute to PD. Although a clinical diagnosis relies on the presence of motor symptoms, including akinesia, rigidity, resting tremor, and postural and balance difficulties, PD is also frequently associated with various non-motor symptoms, such as cognitive dysfunction, mood and psychotic disorder, which negatively affect the patient’s quality of life .
In the central nervous system (CNS), somatostatin (SST) is highly concentrated in a large proportion of GABAergic neurons, where it acts as a co-neurotransmitter or neuromodulator to modulate excitability and neuronal responses [4, 5]. SST has also been recognized as a marker for a particular GABAergic interneuronal subpopulation . The level of SST in cerebrospinal fluid is significantly reduced in PD [7,8,9,10]. However, it has not yet been proven whether GABAergic neurons of PD patients show altered levels of SST.
A potential solution to the difficulty of modeling PD is to use reprogramming technology to generate disease-specific induced pluripotent stem cells (iPSCs). Recently, a method for controlling the regional identity of iPSC-derived neurons along the anteroposterior (A-P) and dorsoventral (D-V) axes was established . In the present study, we evaluated possible changes in the expression level of SST in GABAergic neurons derived from PARK2-specific iPSCs.
Cell culture and neural differentiation
As controls, we used two human iPS cell lines: 201B7 iPSCs purchased from RIKEN BRC and were kindly provided by Dr. Shinya Yamanaka of Kyoto University  and WD39 iPSCs were established by Dr. Yoichi Imaizumi at Keio University. For PARK2 lines, patient A (PA9 and PA22) (female with an exon 2–4 deletion mutation) and patient B (PB2 and PB20) (male with an exon 6–7 deletion mutation) iPSCs were established previously . All of the iPSCs were maintained on feeder cells in iPSC culture media, as described previously . All of the experimental procedures for cell differentiation and analysis were approved by the respective Ethics Committees of Keio University School of Medicine (Approval Number: 20080016) and Hoshi University School of Medicine (Approval Number: 30–006). We applied a previously reported neural differentiation protocol [11, 14] to obtain forebrain GABAergic neurons from human iPSCs. For forebrain GABAergic neural induction, we added a Wnt inhibitor (2 μM IWP-2, FUJIFILM Wako Pure Chemical Corporation, Osaka, Japan) to the culture medium of NPCs from day 0 to day 13 and sonic hedgehog (100 ng/ml Shh, R&D Systems Inc., Minneapolis, MN, USA) and a Shh agonist (1 μM Purmorphamine, Calbiochem, San Diego, CA, USA) to the culture medium of neural progenitor cells (NPCs) from days 2 to 13. Subsequently, NPCs on day 13 were dissociated into single cells using TrypLE™ Select (Thermo Fisher Scientific, Waltham, MA, USA) and seeded on culture dishes coated with poly-L-ornithine (Sigma-Aldrich, St. Louis, MO, USA) and fibronectin (Sigma-Aldrich). For neural differentiation, cells were cultured in KBM Neural Stem Cell medium (KOHJINBIO) containing B27 (Thermo Fisher Scientific), 20 ng/mL brain-derived neurotrophic factor (BDNF, R&D Systems), 20 ng/mL glial cell-derived neurotrophic factor (GDNF, R&D Systems), 200 μM ascorbic acid (Sigma-Aldrich), and 500 μM dibutyryl-cAMP (Sigma-Aldrich).
Quantitative real-time PCR
Total RNA was extracted from control and PARK2-derived cells for each developmental stage, iPSCs, NSCs and differentiated neurons, using TRIzol reagent (Thermo Fisher Scientific) and an RNeasy mini Kit (QIAGEN, Venlo, The Netherlands). Complementary DNA was synthesized using a SuperScript® VILO™ cDNA Synthesis Kit (Thermo Fisher Scientific). Gene expression levels were measured by quantitative real-time PCR (qPCR) on a StepOnePlus™ Real-Time PCR System with a 96-well format. Primer sequences are listed in Additional file 1: Table S1: Quantitative PCR was performed with 5 ng cDNA per well in a 10 μl reaction using Fast SYBR® Green Master Mix (Thermo Fisher Scientific). The data were assessed using the ΔΔ Ct method and normalized by β-actin expression.
Differentiated neurons were fixed with 4% paraformaldehyde and 0.1 M phosphate buffer for 20 min at room temperature. After being washed with PBS, samples were blocked with 5% BSA and 0.3% Triton X-100 in PBS for 1 h. Primary antibodies were diluted in 1% BSA and 0.3% Triton X-100 in PBS and applied at 4 °C overnight. This was followed by incubation with appropriate secondary antibodies (Thermo Fisher Scientific) conjugated with AlexaFluor 488, AlexaFluor 546/594 or AlexaFluor 647 (1:1000) for 90 min at room temperature. Samples were mounted with DAPI-Fluoromount-G™ (SouthernBiotech, Birmingham, AL, USA) and immunoreactive cells were visualized using a BZ-X710 (KEYENCE, Osaka, Japan). The primary antibodies used were as follows: anti-β-III tubulin (1:1000, Sigma-Aldrich), anti-GABA (1:1000, Sigma-Aldrich), anti-SST (1:500, Millipore), Anti-Parvalbumin (PV; 1:2000, Sigma-Aldrich).
All data are presented as the mean ± standard error of mean (SEM). The statistical significance of differences was analyzed by GraphPad Prism (GraphPad Software, La Jolla, CA, USA). For the comparison of multiple groups, statistical analysis was performed using one-way analysis of variance (ANOVA) with Bonferroni’s post-hoc test. Probability values less than 0.05 (p < 0.05) were considered to be statistically significant.
Differentiation of human iPSCs to GABAergic neurons
It has been demonstrated that the A-P identity of iPSC-derived neural progenitors can be controlled by Wnt signaling during neurosphere formation . We applied this previously reported method to generate a GABAergic neuron-enriched culture by treating iPSCs-derived cells with the Porcupine inhibitor IWP-2 , which leads to the formation of forebrain cells, including GABAergic neurons [11, 16]. In addition, Shh activation converted the D-V identity from dorsal to ventral without perturbing the A-P identity . Since GABAergic neurons originate from the medial ganglionic eminence (MGE), we treated cells with the Shh protein and purmorphamine during neurosphere formation (Fig. 1a, b). When neurotrophic factors including BDNF were used for neural maturation, NPCs differentiated into GABAergic neurons (Fig. 1a, b). We next investigated the expression of cell-type-specific markers during differentiation from iPSCs. We confirmed that iPSCs expressed an undifferentiated cell-marker, Oct3/4, while NPCs expressed the neural stem cell marker Nestin (Fig. 1c). Moreover, the GABA-producing enzyme, glutamate decarboxylase (GAD1/67) gradually increased as cell differentiation progressed (Fig. 1c). There were no significant differences of the expression levels of Oct3/4, Nestin and GAD1/67 between control and PD (PA and PB) lines (Fig. 1c). Although we observed a slight increase in the mRNA level of GRIN2B, which is an excitatory neuronal marker, in Day 30 culture neurons compared to that in iPSCs (Fig. 1c, ***p < 0.001 vs. control), GAD1/67 expression was observed with higher levels in control and PARK2 (PA and PB) iPSCs-derived neurons. We also observed the expression of telencephalon-specific D-V markers. The MGE markers ASCL1 and NKX6.2 were highly expressed in NPCs derived from control and PARK2 (PA and PB)-specific iPSCs (Fig. 1e). After 30 days of neural maturation, the differentiated cells were labeled by antibodies to βIII-tubulin (a neuron-specific marker) and GABA (GABAergic neuronal marker) (Fig. 1f). About 80% of βIII-tubulin-positive neurons expressed GABA, indicating successful GABAergic neuronal differentiation (Fig. 1g). Quantitative analyses showed no differences in the potency of differentiation into GABAergic neurons derived from iPSCs between healthy control and PARK2 patients at 30 days (Fig. 1g).
Characterization of GABAergic neurons derived from PARK2-specific iPSCs
Cortical interneurons are conventionally categorized based on neuropeptide and Ca2+ binding protein expression . To characterize GABAergic neurons, we investigated the expression of GABAergic interneuron-specific markers in differentiated cells derived from control and PARK2 (PA and PB)-specific iPSCs. We found that only SST was highly expressed, while the expression of other markers, including PV, nitric oxide synthase (NOS) 1, vasoactive intestinal polypeptide (VIP), cholecystokinin (CCK), calretinin (CR), calbindin (CB), reelin (RELN), neuropeptide Y (NPY) and 5-hydroxytryptamine receptor 3A (HTR3A), was very low in differentiated GABAergic neurons (Fig. 2a). Although SST-positive GABAergic neurons were detected at different levels in differentiated cells derived from control and PARK2 (PA and PB)-specific iPSCs, no PV-positive GABAergic neurons were observed in differentiated cells derived from iPSCs from either source (Fig. 2b). These results suggest that forebrain neurons derived from control and PARK2-specific iPSCs resemble GABAergic interneurons.
Decreased expression of SST in PARK2-specific iPSCs-derived GABAergic neurons
We next investigated possible changes in the expression of SST at 60 days after neural differentiation from control and PARK2-specific iPSCs. We observed a significant decrease in mRNA levels of SST in PARK2 (PA and PB)-specific iPSCs-derived GABAergic neurons at 60 days of differentiation (Fig. 3a, **p < 0.01, ***p < 0.001 vs. control). In GABAergic neurons derived from PARK2-specific iPSCs, the number of SST-positive GABAergic neurons was significantly reduced (Fig. 3c, d), which was also confirmed by the reduction in fluorescence intensity of SST (Fig. 3e). Under these conditions, no significant differences, but slight decreases, in mRNA levels of GAD1/67 in GABAergic neurons were found between healthy control and PARK2 (PA and PB) patients (Fig. 3e). In addition, we found the tendency of the reduction in SST expression normalized with GAD1/67 expression (Additional file 2: Figure S1).
PD is a neurodegenerative disease that is characterized by motor dysfunctions such as tremor, slowness, stiffness, and balance problems. These symptoms are associated with a progressive loss of dopaminergic (DAnergic) neurons in the substantia nigra. However, other classical neurotransmitters such as acetylcholine, glutamate and GABA also play a crucial role in PD-related motor coordination [18,19,20]. On the other hand, PD patients also have non-motor symptoms which are undoubtedly accompanied by a deficit of GABA [21, 22]. In our previous study, we successfully generated DAnergic neuron-enriched culture by treatment with shh, CHIR and purmorphamine during neurosphere formation . By using these cells, we demonstrated that an iPSCs-based model of PARK2 recapitulated the vulnerability of DAnergic neurons with a significant increase in ROS production [23, 24] and ghrelin receptor dysfunction . Recent reports have suggested that the A-P identity, ranging from the telencephalon to the spinal cord, can be controlled by treatment with three factors, IWP-2, CHIR, and RA, during neurosphere formation . In addition to DAnergic neurons, we also generated GABAergic interneuron-enriched culture by treatment of PARK2-specific iPSCs-derived cells with IWP-2, Shh protein and purmorphamine . The molecular composition of GABAergic neurons was diverse, and included the expression of calcium-binding proteins PV, CR and CB, and neuropeptides, such as SST, NPY, CCK and VIP . In recent studies, different subgroups of GABAergic interneurons, including CR, CB, CCK, PV, SST and NPY, have been identified by immunohistochemistry and systematically counted in the anterior cingulate, prelimbic and infralimbic cortices . To characterize the present GABAergic neurons derived from iPSCs, we investigated the expression of subtype-specific markers. As a result, only SST was highly expressed, while other markers (PV, NOS1, VIP, CCK, CR, CB, RELN, NPY and HTR3A) were seen at very low levels.
SST, which inhibits several biologically active substances such as growth hormone (GH) and insulin [28, 29], is abundant throughout the CNS . SST acts as a neurotransmitter (co-transmitter) or neuromodulator and plays a role in the fine-tuning of neuronal activity and synaptic plasticity. The changes in GABAergic function in neural microcircuits could result in modulation of the excitatory-inhibitory imbalance via the release of SST. It has been considered that the decreased SST levels in the frontal and entorhinal cortex as well as the hippocampus lead to the cognitive deficits in patients with PD . Furthermore, the expression levels of CB, SST and CCK, which are markers of inhibitory neuronal subpopulations in GABAergic interneurons of the frontal cortex, are known to be negatively correlated with age . In the present study, we found that the mRNA level of SST and the number of SST-positive GABAergic neurons were clearly decreased in GABAergic interneurons derived from PARK2 patient-specific iPSCs. In the previous study, PARK2 mutations lost the ability to suppress MAO transcription and resulted in elevation of oxidative stress in PARK2 iPS-derived DAnergic neurons . A recent study suggested that SST exerted neuroprotective effects against the lipopolysaccharide (LPS)-mediated loss of TH-positive DA neurons in the substantia nigra of a PD model . Although further studies are needed to investigate the role of SST in the dysfunction of the neural network in PD, we hypothesize that PARK2 mutations somehow could affect the gene transcription and mitochondrial dysfunction in SST-expressing GABAergic neurons.
In conclusion, the present study clearly indicated that the level of SST was reduced in differentiated GABAergic interneurons from PARK2-specific iPSCs derived from PD patients. We propose that the deficiency of SST in GABAergic neurons of the frontal cortex may lead to the motor and/or non-motor symptoms of PD via the regulation of the excitatory-inhibitory imbalance of the neural network.
Brain-derived neurotrophic factor
Bovine serum albumin
Central nervous system
Fetal bovine serum
Gamma amino butyric acid
Glutamate decarboxylase 1/67
Glial cell-derived neurotrophic factor
5-hydroxytryptamine receptor 3A
Induced pluripotent stem cell
Nitric oxide synthase
Neural progenitor cell
Vasoactive intestinal polypeptide
Dorsey ER, Constantinescu R, Thompson JP, Biglan KM, Holloway RG, Kieburtz K, et al. Projected number of people with Parkinson disease in the most populous nations, 2005 through 2030. Neurology. 2007;68(5):384–6.
Masliah E, Rockenstein E, Veinbergs I, Mallory M, Hashimoto M, Takeda A, et al. Dopaminergic loss and inclusion body formation in alpha-synuclein mice: implications for neurodegenerative disorders. Science. 2000;287(5456):1265–9.
Chaudhuri KR, Healy DG, Schapira AH. National Institute for clinical E. Non-motor symptoms of Parkinson's disease: diagnosis and management. Lancet Neurol. 2006;5(3):235–45.
Viollet C, Lepousez G, Loudes C, Videau C, Simon A, Epelbaum J. Somatostatinergic systems in brain: networks and functions. Mol Cell Endocrinol. 2008;286(1–2):75–87.
Liguz-Lecznar M, Urban-Ciecko J, Kossut M. Somatostatin and somatostatin-containing neurons in shaping neuronal activity and plasticity. Front Neural Circuits. 2016;10:48.
Wonders CP, Anderson SA. The origin and specification of cortical interneurons. Nat Rev Neurosci. 2006;7(9):687–96.
Ionov ID, Pushinskaya II. Somatostatin antagonist induces catalepsy in the aged rat. Psychopharmacology. 2013;227(2):273–6.
Dupont E, Christensen SE, Hansen AP, de Fine Olivarius B, Orskov H. Low cerebrospinal fluid somatostatin in Parkinson disease: an irreversible abnormality. Neurology. 1982;32(3):312–4.
Epelbaum J, Ruberg M, Moyse E, Javoy-Agid F, Dubois B, Agid Y. Somatostatin and dementia in Parkinson's disease. Brain Res. 1983;278(1–2):376–9.
Strittmatter M, Hamann GF, Strubel D, Cramer H, Schimrigk K. Somatostatin-like immunoreactivity, its molecular forms and monoaminergic metabolites in aged and demented patients with Parkinson's disease--effect of L-Dopa. J Neural Transm (Vienna). 1996;103(5):591–602.
Imaizumi K, Sone T, Ibata K, Fujimori K, Yuzaki M, Akamatsu W, et al. Controlling the regional identity of hPSC-derived neurons to uncover neuronal subtype specificity of neurological disease phenotypes. Stem Cell Reports. 2015;5(6):1010–22.
Takahashi K, Tanabe K, Ohnuki M, Narita M, Ichisaka T, Tomoda K, et al. Induction of pluripotent stem cells from adult human fibroblasts by defined factors. Cell. 2007;131(5):861–72.
Imaizumi Y, Okada Y, Akamatsu W, Koike M, Kuzumaki N, Hayakawa H, et al. Mitochondrial dysfunction associated with increased oxidative stress and alpha-synuclein accumulation in PARK2 iPSC-derived neurons and postmortem brain tissue. Mol Brain. 2012;5:35.
Fujimori K, Matsumoto T, Kisa F, Hattori N, Okano H, Akamatsu W. Escape from pluripotency via inhibition of TGF-beta/BMP and activation of Wnt signaling accelerates differentiation and aging in hPSC progeny cells. Stem Cell Reports. 2017;9(5):1675–91.
Chen B, Dodge ME, Tang W, Lu J, Ma Z, Fan CW, et al. Small molecule-mediated disruption of Wnt-dependent signaling in tissue regeneration and cancer. Nat Chem Biol. 2009;5(2):100–7.
Yuan F, Fang KH, Cao SY, Qu ZY, Li Q, Krencik R, et al. Efficient generation of region-specific forebrain neurons from human pluripotent stem cells under highly defined condition. Sci Rep. 2015;5:18550.
Petilla Interneuron Nomenclature G, Ascoli GA, Alonso-Nanclares L, Anderson SA, Barrionuevo G, Benavides-Piccione R, et al. Petilla terminology: nomenclature of features of GABAergic interneurons of the cerebral cortex. Nat Rev Neurosci. 2008;9(7):557–68.
Yu X, He GR, Sun L, Lan X, Shi LL, Xuan ZH, et al. Assessment of the treatment effect of baicalein on a model of parkinsonian tremor and elucidation of the mechanism. Life Sci. 2012;91(1–2):5–13.
O'Gorman Tuura RL, Baumann CR, Baumann-Vogel H. Beyond dopamine: GABA, glutamate, and the axial symptoms of Parkinson disease. Front Neurol. 2018;9:806.
Manyam BV. Low CSF gamma-aminobutyric acid levels in Parkinson's disease. Effect of levodopa and carbidopa. Arch Neurol. 1982;39(7):391–2.
Blaszczyk JW. Parkinson's disease and neurodegeneration: GABA-collapse hypothesis. Front Neurosci. 2016;10:269.
Tong Q, Xu Q, Xia Q, Yuan Y, Zhang L, Sun H, et al. Correlations between plasma levels of amino acids and nonmotor symptoms in Parkinson’s disease. J Neural Transm. 2014;122(3):411–7.
Matsumoto T, Fujimori K, Andoh-Noda T, Ando T, Kuzumaki N, Toyoshima M, et al. Functional neurons generated from T cell-derived induced pluripotent stem cells for neurological disease modeling. Stem Cell Reports. 2016;6(3):422–35.
Suzuki S, Akamatsu W, Kisa F, Sone T, Ishikawa KI, Kuzumaki N, et al. Efficient induction of dopaminergic neuron differentiation from induced pluripotent stem cells reveals impaired mitophagy in PARK2 neurons. Biochem Biophys Res Commun. 2017;483(1):88–93.
Suda Y, Kuzumaki N, Sone T, Narita M, Tanaka K, Hamada Y, et al. Down-regulation of ghrelin receptors on dopaminergic neurons in the substantia nigra contributes to Parkinson's disease-like motor dysfunction. Mol Brain. 2018;11(1):6.
Gentet LJ. Functional diversity of supragranular GABAergic neurons in the barrel cortex. Front Neural Circuits. 2012;6:52.
Czeh B, Vardya I, Varga Z, Febbraro F, Csabai D, Martis LS, et al. Long-term stress disrupts the structural and functional integrity of GABAergic neuronal networks in the medial prefrontal cortex of rats. Front Cell Neurosci. 2018;12:148.
Thorner MO, Vance ML, Hartman ML, Holl RW, Evans WS, Veldhuis JD, et al. Physiological role of somatostatin on growth hormone regulation in humans. Metabolism. 1990;39(9 Suppl 2):40–2.
D'Alessio DA, Sieber C, Beglinger C, Ensinck JW. A physiologic role for somatostatin 28 as a regulator of insulin secretion. J Clin Invest. 1989;84(3):857–62.
Epelbaum J, Guillou JL, Gastambide F, Hoyer D, Duron E, Viollet C. Somatostatin, Alzheimer's disease and cognition: an old story coming of age? Prog Neurobiol. 2009;89(2):153–61.
Mohan A, Thalamuthu A, Mather KA, Zhang Y, Catts VS, Weickert CS, et al. Differential expression of synaptic and interneuron genes in the aging human prefrontal cortex. Neurobiol Aging. 2018;70:194–202.
Jiang H, Ren Y, Yuen EY, Zhong P, Ghaedi M, Hu Z, et al. Parkin controls dopamine utilization in human midbrain dopaminergic neurons derived from induced pluripotent stem cells. Nat Commun. 2012;3:668.
Bai L, Zhang X, Li X, Liu N, Lou F, Ma H, et al. Somatostatin prevents lipopolysaccharide-induced neurodegeneration in the rat substantia nigra by inhibiting the activation of microglia. Mol Med Rep. 2015;12(1):1002–8.
We thank Dr. Yoichi Imaizumi (Keio University) for providing PARK2-specific iPS cells and prof. Shinya Yamanaka (Kyoto University) for providing 201B7 iPS cells.
CI, NK, YS, RK and YO performed experiments; NK, NH, HO and MN supervised the research; CI, YS, NK and MN wrote the manuscript. All authors read and approved the final manuscript.
This work was supported by MEXT-Supported Program for the Strategic Research Foundation at Private Universities, 2014–2018, S1411019 to M.N. This research was supported by Hoshi University.
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All of the data generated and analyzed in this study are included in the published article.
Ethics approval and consent to participate
All of the experimental procedures for cell differentiation and analysis were approved by the respective Ethics Committees of Keio University School of Medicine Approval Number: 20080016) and Hoshi University School of Medicine (Approval Number: 30–006).
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Written informed consent to publish was obtained from the patient and the healthy donor.
The authors declare that they have no competing interests
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Additional file 1:
Table S1. Real-time PCR primer. (PDF 99.6 kb)
Additional file 2:
Figure S1. Expression of SST in GABAergic neurons normalized with GAD1/67 expression. Quantitative gene-expression analysis of SST in control and PARK2 (PA and PB) iPSC-derived GABAergic neurons (day 60) normalized with GAD1/67 expression. (TIFF 97.3 kb)
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Iwasawa, C., Kuzumaki, N., Suda, Y. et al. Reduced expression of somatostatin in GABAergic interneurons derived from induced pluripotent stem cells of patients with parkin mutations. Mol Brain 12, 5 (2019). https://doi.org/10.1186/s13041-019-0426-7
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