Lee Sun Kyong, Sillitoe Roy V, Silva Coralie, Martina Marco, Sekerkova Gabriella
Department of Physiology, Feinberg School of Medicine, Northwestern University, Morton 5-619, Chicago, IL, 60611, USA.
Department of Pathology and Immunology, Baylor College of Medicine, Jan and Dan Duncan Neurological Research Institute of Texas Children's Hospital, Houston, TX, 77030, USA.
Cerebellum. 2015 Oct;14(5):516-27. doi: 10.1007/s12311-015-0673-9.
α-Synuclein has a crucial role in synaptic vesicle release and synaptic membrane recycling. Although its general expression pattern has been described in the cerebellum, the precise cerebellar structures where α-synuclein is localized are poorly understood. To address this question, we used α-synuclein immunohistochemistry in adult mice cerebellar sections. We found that α-synuclein labels glutamatergic but not glycinergic and GABAergic synaptic terminals in the molecular and granule cell layers. α-Synuclein was preferentially expressed in parallel and mossy fiber synaptic terminals that also express vesicular glutamate transporter 1 (VGluT1), while it was not detected in VGluT2-positive climbing fibers. α-Synuclein was particularly enriched in lobules IX and X, a region known to contain a high density of unipolar brush cells (UBCs). To elucidate whether the α-synuclein-positive mossy fibers belong to UBCs, we double-labeled cerebellar sections with antibodies to α-synuclein and UBC-type-specific markers (calretinin for type I and metabotropic glutamate receptor 1α (mGluR1α) for type II UBCs) and took advantage of organotypic cerebellar cultures (in which all mossy fibers are UBC axons) and moonwalker mice (in which almost all UBCs are ablated) and found that both type I and type II UBCs express α-synuclein. In moonwalker mutant cerebella, the α-synuclein/VGluT1 immunolabeling showed a dramatic decrease in the vestibulocerebellum that correlated with the absence of UBC. α-Synuclein appears to be an excellent marker for intrinsic mossy fibers of the VGluT1 subset in conjunction with UBCs of both subtypes.
α-突触核蛋白在突触小泡释放和突触膜循环中起关键作用。尽管其在小脑的一般表达模式已被描述,但α-突触核蛋白在小脑的确切定位结构仍知之甚少。为了解决这个问题,我们在成年小鼠小脑切片中使用了α-突触核蛋白免疫组织化学方法。我们发现,α-突触核蛋白标记分子层和颗粒细胞层中的谷氨酸能突触终末,而不标记甘氨酸能和GABA能突触终末。α-突触核蛋白优先表达于同时表达囊泡谷氨酸转运体1(VGluT1)的平行纤维和苔藓纤维突触终末,而在VGluT2阳性的攀缘纤维中未检测到。α-突触核蛋白在小叶IX和X中特别富集,该区域已知含有高密度的单极刷细胞(UBCs)。为了阐明α-突触核蛋白阳性的苔藓纤维是否属于UBCs,我们用针对α-突触核蛋白和UBC类型特异性标记物(I型用钙视网膜蛋白,II型UBCs用代谢型谷氨酸受体1α(mGluR1α))的抗体对小脑切片进行双重标记,并利用小脑器官型培养物(其中所有苔藓纤维都是UBC轴突)和月球漫步者小鼠(其中几乎所有UBCs都被切除),发现I型和II型UBCs均表达α-突触核蛋白。在月球漫步者突变体小脑中,α-突触核蛋白/VGluT1免疫标记显示前庭小脑中有显著减少,这与UBCs的缺失相关。α-突触核蛋白似乎是与两种亚型的UBCs结合的VGluT1亚群内在苔藓纤维的优良标记物。