Enhanced expression of 14-3-3 family members in injured motoneurons

被引:42
作者
Namikawa, K [1 ]
Su, QN [1 ]
Kiryu-Seo, S [1 ]
Kiyama, H [1 ]
机构
[1] Asahikawa Med Coll, Dept Anat, Asahikawa, Hokkaido 0788510, Japan
来源
MOLECULAR BRAIN RESEARCH | 1998年 / 55卷 / 02期
基金
日本学术振兴会;
关键词
Raf-1; Erk; Ras; bad; nerve regeneration; differential display; rat;
D O I
10.1016/S0169-328X(98)00012-6
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
An increase in 14-3-3 mRNA expression after hypoglossal nerve injury was demonstrated by RNA finger printing using the arbitrary primed polymerase chain reaction (RAP-PCR). RAP-PCR was carried out to compare differences in mRNA expression between axotomized (6 h after the transection) and normal hypoglossal nuclei in mice. The expression of several gene fragments was increased after nerve injury; one fragment was identified as 14-3-3 which is an activator of Raf-l. Since a family of 14-3-3 genes are identified in the rat, we examined the expression of five members of the rat 14-3-3 family after injury (beta, gamma, zeta, eta and theta). Among these family members, a substantial up-regulation in mRNA expression was observed for the zeta and theta forms. Subsequent emulsion autoradiography of hybridization tissue sections revealed an increase in zeta and theta mRNA in injured motoneurons. Since 14-3-3 has the ability to dimerize and activate Raf-1 the up-regulation of 14-3-3 expression would be expected to facilitate the Ras-Erk signal pathway by Raf-l activation. Our previous results have demonstrated that Shc, Erk1 and Mek1 mRNAs are up-regulated during nerve regeneration, whereas PKA which inhibits the Ras-Erk pathway via Raf-1 was down-regulated. Taken together, the present results suggest that enhancement in expression of molecules involved in the Ras-Erk signaling is required for peripheral nerve regeneration. (C) 1998 Elsevier Science B.V.
引用
收藏
页码:315 / 320
页数:6
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