Cell density increases Bcl-2 and Bcl-x expression in addition to survival of cultured cerebellar granule neurons

被引:17
|
作者
Ohga, Y
Zirrgiebel, U
Hamner, S
Michaelidis, TM
Cooper, J
Thoenen, H
Lindholm, D
机构
[1] MAX PLANCK INST PSYCHIAT,DEPT NEUROCHEM,D-82152 PLANEGG,GERMANY
[2] CTR BIOMED,DEPT DEV NEUROSCI,S-75123 UPPSALA,SWEDEN
关键词
D O I
10.1016/0306-4522(96)00204-7
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The proto-oncogene bcl-2 and its family members, bcl-x and bar are recognized as major regulators of cell death and survival, Although Bcl-2 and Bcl-x are expressed in brain, little is known how they are regulated in neurons. Here we have studied the expression of bcl-2, bcl-xL and bar mRNA in rat cerebellar granule neurons cultured under conditions which influence neuron survival, Insulin-like growth factor-1 and brain-derived neurotrophic factor supported the survival of these neurons, but affected neither the expression of bcl-2, bcl-xL nor bar mRNA. In contrast, bcl-2 and bcl-xL mRNAs were up-regulated in cerebellar granule neurons plated at high density exhibiting an increased neuronal survival, Western blots showed that cell density also increased Bcl-2 protein level. However, conditioned medium from dense cultures did not affect the level of bcl-2 mRNA nor survival of the neurons. This suggests that cell density promotes survival and regulates Bcl-2 expression in cerebellar granule neurons through a signaling pathway different from known neurotrophic factors. Copyright (C) 1966 IBRO.
引用
收藏
页码:913 / 917
页数:5
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