DEVELOPMENTAL EXPRESSION OF THE PROTEIN-KINASE-C FAMILY IN RAT HIPPOCAMPUS

被引:41
|
作者
JIANG, XL
NAIK, MU
HRABE, J
SACKTOR, TC
机构
[1] SUNY HLTH SCI CTR,DEPT PHARMACOL,MOLEC NEUROSCI LAB,BROOKLYN,NY 11203
[2] SUNY HLTH SCI CTR,DEPT NEUROL,BROOKLYN,NY 11203
[3] YESHIVA UNIV ALBERT EINSTEIN COLL MED,DEPT NEUROSCI,BRONX,NY 10461
来源
DEVELOPMENTAL BRAIN RESEARCH | 1994年 / 78卷 / 02期
关键词
PROTEIN KINASE M; ZETA; SYNAPTIC PLASTICITY; PHOSPHORYLATION; LONG-TERM POTENTIATION;
D O I
10.1016/0165-3806(94)90038-8
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Protein kinase C (PKC) is a heterogeneous family of ten or more isoforms which plays an important role in neuronal signal transduction. Isoforms from all subclasses are prominently expressed in the rat hippocampus, as demonstrated by immunoblot with isozyme-specific antisera: Ca2+-dependent (alpha, beta I, beta II and gamma), Ca2+-independent (delta, epsilon and a newly characterized PKC related to eta) and atypical(zeta). In addition, the zeta isoform is also found as the free, constitutively active catalytic domain, protein kinase M zeta (PKM zeta). Two distinct patterns of expression of PKC isozymes in rat hippocampus are found during development from E18 to P28. PKC zeta, PKM zeta and PKC delta are present at birth and their expression does not increase postnatally. In contrast, the other isoforms are expressed only at low levels at birth and then increase in the first 4 weeks postnatally. These two patterns of expression suggest distinct functions for PKC isozymes during development.
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页码:291 / 295
页数:5
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