Differential expression of bcl-w and bcl-x messenger RNA in the developing and adult rat nervous system

被引:54
作者
Hamnér, S [1 ]
Skoglösa, Y [1 ]
Lindholm, D [1 ]
机构
[1] Dept Neurosci Dev Neurosci, S-75123 Uppsala, Sweden
关键词
brain development; gene regulation; bcl-2; in situ hybridization; neuronal culture; cell death;
D O I
10.1016/S0306-4522(98)00642-3
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The bcl-2 family of proteins comprises both anti-apoptotic and pro-apoptotic members, which play a pivotal role in regulating cell death. Bcl-w is a recently identified member of this family, which was shown to inhibit apoptosis in haemopoietic cell lines. However, the function and expression patterns of bcl-w in the nervous system have so far not been described. We have cloned complementary DNA corresponding to rat bcl-w and analysed the expression of bcl-w messenger RNA during rat brain development, using RNA blotting and in situ hybridization techniques. We also compared the expression patterns of bcl-w with those of bcl-x(L). During brain development, the levels of bcl-w messenger RNA were found to increase, with highest expression located to specific regions of the mature brain, such as hippocampus, cerebellum, piriform cortex and locus coeruleus. Bcl-w messenger RNA was expressed by neurons, as shown with double labeling with neuronal markers. In contrast to bcl-w, bcl-x(L) messenger RNA expression levels were highest during early development, particularly in cortex, hippocampus, thalamus, spinal cord and dorsal root ganglia. During postnatal development the expression of bcl-x(L) messenger RNA decreased and were only detected at low levels in the adult nervous system. As shown earlier for bcl-2, the expression of bcl-w and bcl-x messenger RNA in cultured cerebellar granule cells was not altered by the deprivation of neurotrophic factors. The present results suggest that bcl-w may play an important role in the mature nervous system. (C) 1999 IBRO. Published by Elsevier Science Ltd.
引用
收藏
页码:673 / 684
页数:12
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