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胶质细胞源性神经营因子诱导的神经突形成受到蛋白激酶抑制剂的刺激,并受到Ras抑制剂的抑制。

GDNF-induced neurite formation was stimulated by protein kinase inhibitors and suppressed by Ras inhibitors.

作者信息

Hiwasa T, Kondo K, Hishiki T, Koshizawa S, Umezawa K, Nakagawara A

机构信息

Department of Biochemistry, School of Medicine, Chiba University, Japan.

出版信息

Neurosci Lett. 1997 Dec 5;238(3):115-8. doi: 10.1016/s0304-3940(97)00861-6.

Abstract

The effects of various inhibitors on the glial cell line-derived neurotrophic factor (GDNF)-induced neurite formation in TGW human neuroblastoma cells were investigated. Treatment of cells with Ser/Thr protein kinase inhibitors such as staurosporine, H-7, H-8 and HA-1004, induced neurite formation without GDNF. On the other hand, tyrosine kinase inhibitors such as erbstatin, genistein and herbimycin A did not produce neurites per se, but effectively enhanced the GDNF-induced neurite formation. A phosphatase inhibitor, okadaic acid, and Ras inhibitors such as oxanosine, damnacanthal and conophylline strongly suppressed the effect of GDNF. These results suggest that a tyrosine protein kinase has a suppressive role in the neurite formation induced by GDNF and that Ras is necessary for the signaling initiated by GDNF.

摘要

研究了各种抑制剂对TGW人神经母细胞瘤细胞中胶质细胞源性神经营养因子(GDNF)诱导的神经突形成的影响。用丝氨酸/苏氨酸蛋白激酶抑制剂(如星形孢菌素、H-7、H-8和HA-1004)处理细胞,可在无GDNF的情况下诱导神经突形成。另一方面,酪氨酸激酶抑制剂(如埃博霉素、染料木黄酮和除莠霉素A)本身不会产生神经突,但能有效增强GDNF诱导的神经突形成。磷酸酶抑制剂冈田酸和Ras抑制剂(如氧杂环丁烷、虎刺醛和锥丝碱)强烈抑制GDNF的作用。这些结果表明,酪氨酸蛋白激酶在GDNF诱导的神经突形成中具有抑制作用,并且Ras是GDNF启动信号所必需的。

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