TGF-β1 inhibits caspase-3 activation and neuronal apoptosis in rat hippocampal cultures

被引:69
|
作者
Zhu, Y [1 ]
Ahlemeyer, B [1 ]
Bauerbach, E [1 ]
Krieglstein, J [1 ]
机构
[1] Univ Marburg, Inst Pharmakol & Toxikol, D-35032 Marburg, Germany
关键词
TGF-beta; 1; neuronal apoptosis; caspase-3; staurosporine; rat primary hippocampal culture;
D O I
10.1016/S0197-0186(00)00084-X
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The effect of TGF-beta1 an apoptosis varies depending on the cell type, the kind of stimulus and the experimental conditions. The present study attempted to identify whether TGF-beta1 can prevent neuronal apoptosis and interrupt caspase-3 activation in rat primary hippocampal cultures after staurosporine treatment. TGF-beta1 at the concentration of 1 and 10 ng/ml significantly reduced neuronal damage as detected by trypan blue exclusion. Nuclear staining with Hoechst 33258 and TUNEL-staining further demonstrated that TGF-beta1 at the same concentration range effectively diminished neuronal apoptosis 24 h after staurosporine treatment, whereas 0.1 ng/ml of TGF-beta1 did not. Furthermore, TGF-beta1 (1 and 10 ng/ml) markedly inhibited the activation of caspase-3 induced by staurosporine as demonstrated by both caspase-3 activity assay and Western blotting. This study provides evidence that TGF-beta1 is able to efficiently inhibit caspase-3 activation, and thereby protects cultured hippocampal neurons against apoptosis. (C) 2001 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:227 / 235
页数:9
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