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大鼠黑质纹状体神经元表达胶质细胞系源性神经营养因子受体亚基c-RET。

Nigrostriatal neurons in rat express the glial cell line-derived neurotrophic factor receptor subunit c-RET.

作者信息

Wang Yan-Qin, Bian Gan-Lan, Wei Li-Chun, Cao Rong, Peng Yi-Feng, Chen Liang-Wei

机构信息

Institute of Neurosciences, The Fourth Military Medical University, Xi'an, People's Republic of China.

出版信息

Anat Rec (Hoboken). 2008 Jan;291(1):49-54. doi: 10.1002/ar.20618.

DOI:10.1002/ar.20618
PMID:18085609
Abstract

The substantia nigra neurons expressing c-RET, a glial cell line-derived neurotrophic factor (GDNF) receptor intracellular tyrosine kinase subunit, were investigated in rats by using a double labeling method which combined retrograde horseradish peroxidase (HRP) labeling after injection into the striatum with immunohistochemistry to c-RET. It was revealed that the distribution of c-RET-immunoreactive neurons and HRP-labeled nigrostriatal neurons overlapped. Numerous double-labeled HRP/c-RET neurons were found in the substantia nigra pars compacta with predominate distribution ipsilateral to the injected striatum. Semiquantitative cell count indicated that a large percentage (97%) of HRP-labeled neurons showed c-RET immunoreactivity. Furthermore, double-labeled HRP/c-RET ones constituted only 61% of total c-RET-immunoreactive neurons in the substantia nigra ipsolateral to the injected striatum. Taken together with previous observations on glial cell line-derived neurotrophic factor in the basal ganglia, this study provides evidence that the c-RET protein may mediate biological activity of GDNF family ligands in most of projecting neurons in the substantia nigra pars compacta where the dopaminergic neurons are numerously distributed. Specially, it suggests that c-RET-mediating signaling cascades may play important roles in neuron-glial interaction that support and sustain nigrostriatal neuronal circuits in the basal ganglia.

摘要

采用双重标记法研究大鼠中表达胶质细胞源性神经营养因子(GDNF)受体细胞内酪氨酸激酶亚基c-RET的黑质神经元。该方法是将辣根过氧化物酶(HRP)逆行注射到纹状体后进行标记,并结合c-RET免疫组织化学方法。结果显示,c-RET免疫反应性神经元与HRP标记的黑质纹状体神经元分布重叠。在黑质致密部发现大量双重标记的HRP/c-RET神经元,主要分布在注射侧纹状体的同侧。半定量细胞计数表明,大部分(97%)HRP标记的神经元呈现c-RET免疫反应性。此外,双重标记的HRP/c-RET神经元仅占注射侧纹状体同侧黑质中c-RET免疫反应性神经元总数的61%。结合先前对基底神经节中胶质细胞源性神经营养因子的观察,本研究提供了证据,表明c-RET蛋白可能在多巴胺能神经元大量分布的黑质致密部的大多数投射神经元中介导GDNF家族配体的生物活性。特别地,这表明c-RET介导的信号级联可能在支持和维持基底神经节黑质纹状体神经回路的神经元-胶质细胞相互作用中发挥重要作用。

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Nigrostriatal neurons in rat express the glial cell line-derived neurotrophic factor receptor subunit c-RET.大鼠黑质纹状体神经元表达胶质细胞系源性神经营养因子受体亚基c-RET。
Anat Rec (Hoboken). 2008 Jan;291(1):49-54. doi: 10.1002/ar.20618.
2
Nigrostriatal projecting neurons express GDNF receptor subunit RET in adult rats.黑质纹状体投射神经元在成年大鼠中表达胶质细胞源性神经营养因子受体亚基RET。
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Absence of Ret signaling in mice causes progressive and late degeneration of the nigrostriatal system.小鼠中Ret信号缺失会导致黑质纹状体系统进行性晚期退化。
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ret receptor tyrosine kinase immunoreactivity is altered in glial cell line-derived neurotrophic factor-responsive neurons following lesions of the nigrostriatal and septohippocampal pathways.在黑质纹状体和隔海马通路损伤后,胶质细胞源性神经营养因子反应性神经元中的ret受体酪氨酸激酶免疫反应性发生改变。
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RET expression does not change with age in the substantia nigra pars compacta of rhesus monkeys.在恒河猴黑质致密部中,RET表达不会随年龄变化。
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Intrastriatal administration of human immunodeficiency virus-1 glycoprotein 120 reduces glial cell-line derived neurotrophic factor levels and causes apoptosis in the substantia nigra.纹状体内注射人类免疫缺陷病毒1型糖蛋白120会降低胶质细胞源性神经营养因子水平,并导致黑质细胞凋亡。
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Striatal GDNF administration increases tyrosine hydroxylase phosphorylation in the rat striatum and substantia nigra.纹状体内给予胶质细胞源性神经营因子可增加大鼠纹状体和黑质中酪氨酸羟化酶的磷酸化水平。
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Striatal expression of GDNF and differential vulnerability of midbrain dopaminergic cells.纹状体内胶质细胞源性神经营养因子的表达与中脑多巴胺能细胞的不同易损性
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Injury induced c-Jun expression and phosphorylation in the dopaminergic nigral neurons of the rat: correlation with neuronal death and modulation by glial-cell-line-derived neurotrophic factor.损伤诱导大鼠多巴胺能黑质神经元中c-Jun的表达和磷酸化:与神经元死亡的相关性及胶质细胞源性神经营养因子的调节作用
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Glial cell line-derived neurotrophic factor receptor GFRalpha1 is expressed in the rat striatum during postnatal development.胶质细胞系源性神经营养因子受体GFRalpha1在大鼠出生后发育期间的纹状体中表达。
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