首页> 外文期刊>Neuroscience: An International Journal under the Editorial Direction of IBRO >Identification of human SEP1 as a glial cell line-derived neurotrophic factor-inducible protein and its expression in the nervous system.
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Identification of human SEP1 as a glial cell line-derived neurotrophic factor-inducible protein and its expression in the nervous system.

机译:鉴定人SEP1为胶质细胞源性神经营养因子诱导蛋白及其在神经系统中的表达。

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摘要

Glial cell line-derived neurotrophic factor (GDNF) signals through multisubunit receptor complex consisting of RET tyrosine kinase and a glycosylphosphatidylinositol-anchored coreceptor called GDNF family receptor alpha1 (GFRalpha1). In the current study, we cloned a human SEP1 gene as a GDNF-inducible gene using human neuroblastoma cells that express RET and GFRalpha1. The induction of the SEP1 gene showed two peaks at 0.5-2 h and 24-48 h after GDNF stimulation by Northern blotting and quantitative real-time reverse transcriptase polymerase chain reaction. The late induction was also confirmed at protein levels by Western blotting with anti-SEP1 antibody. Immunostaining revealed that the expression of the SEP1 protein was detected in cell body, elongated neurites and growth cone-like structure of neuroblastoma cells treated with GDNF. In addition, we found a high level of SEP1 expression in neurons of the dorsal root and superior cervical ganglia and motor neurons of the spinal cord of mice in which RET is also expressed. SEP1 was co-immunoprecipitated with alpha- and beta-tubulins from the lysate of mouse brain. These results thus suggested that SEP1 is a GDNF-inducible and microtubule-associated protein that may play a role in the nervous system.
机译:胶质细胞源性神经营养因子(GDNF)通过由RET酪氨酸激酶和糖基磷脂酰肌醇固定的共受体GDNF家族受体alpha1(GFRalpha1)组成的多亚基受体复合物发出信号。在当前的研究中,我们使用表达RET和GFRalpha1的人神经母细胞瘤细胞克隆了人SEP1基因作为GDNF诱导基因。通过Northern印迹和定量实时逆转录酶聚合酶链反应在GDNF刺激后,SEP1基因的诱导在0.5-2 h和24-48 h显示两个峰。还通过抗SEP1抗体的蛋白质印迹在蛋白质水平上证实了晚期诱导。免疫染色显示,在用GDNF处理的神经母细胞瘤细胞中,在细胞体,伸长的神经突和生长锥状结构中检测到SEP1蛋白的表达。另外,我们在还表达RET的小鼠的背根和上颈神经节的神经元以及脊髓的运动神经元中发现了高水平的SEP1表达。 SEP1与来自小鼠大脑溶解产物的α-和β-微管蛋白共免疫沉淀。因此,这些结果表明,SEP1是GDNF诱导的微管相关蛋白,可能在神经系统中起作用。

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