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神经生长因子、蛋白激酶C激活剂及钙离子载体对PC12细胞培养物中Thy-1和神经细胞黏附分子表达影响的比较

Comparison of the effects of NGF, activators of protein kinase C, and a calcium ionophore on the expression of Thy-1 and N-CAM in PC12 cell cultures.

作者信息

Doherty P, Mann D A, Walsh F S

机构信息

Institute of Neurology, Queen Square, London, United Kingdom.

出版信息

J Cell Biol. 1988 Jul;107(1):333-40. doi: 10.1083/jcb.107.1.333.

Abstract

The addition of nerve growth factor (NGF) to PC12 cells induces an approximate doubling in the cell surface expression of the Thy-1 glycoprotein and the neural cell adhesion molecule (N-CAM) after 24 h of culture. Although both responses are measured at the same time point, their sensitivity to NGF differed with half-maximal induction of Thy-1 apparent at NGF concentrations (approximately 0.1 ng/ml NGF) that had little effect on N-CAM expression. Phorbol ester derivatives capable of activating Ca2+/phospholipid-dependent protein kinase (protein kinase C) and the calcium ionophore A23187 were found to mimic the NGF induction of Thy-1, but not N-CAM. Similar results were observed when a synthetic diacylglycerol was added to PC12 cell cultures. Increased expression of Thy-1 consequent to phorbol ester, calcium ionophore, or NGF treatment was associated with an increase in the expression of the mRNA species that encodes Thy-1. Increased expression of Thy-1 consequent to all three treatments was also reduced by treatment with the transcription inhibitor cordycepin. Treatment of PC12 cells with high concentrations of phorbol esters was found to inhibit the NGF induction of Thy-1, but not N-CAM. Whereas the above results are consistent with activation of protein kinase C underlying the NGF induction of Thy-1, the same data are not consistent with this pathway being important in the N-CAM response.

摘要

在PC12细胞中添加神经生长因子(NGF),培养24小时后,Thy-1糖蛋白和神经细胞黏附分子(N-CAM)的细胞表面表达量会增加约一倍。虽然这两种反应是在同一时间点测量的,但它们对NGF的敏感性不同,Thy-1在NGF浓度(约0.1 ng/ml NGF)下出现半数最大诱导,而该浓度对N-CAM表达几乎没有影响。能够激活Ca2+/磷脂依赖性蛋白激酶(蛋白激酶C)的佛波酯衍生物和钙离子载体A23187被发现可模拟NGF对Thy-1的诱导作用,但对N-CAM无此作用。当向PC12细胞培养物中添加合成二酰甘油时,也观察到了类似结果。佛波酯、钙离子载体或NGF处理导致的Thy-1表达增加与编码Thy-1的mRNA种类表达增加有关。用转录抑制剂放线菌素D处理后,这三种处理导致的Thy-1表达增加也均降低。发现用高浓度佛波酯处理PC12细胞可抑制NGF对Thy-1的诱导作用,但对N-CAM无此作用。虽然上述结果与蛋白激酶C的激活是NGF诱导Thy-1的基础一致,但相同数据并不支持该途径在N-CAM反应中起重要作用。

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