CHARACTERIZATION AND DIFFERENTIAL EXPRESSION OF PROTEIN-KINASE-C ISOFORMS IN PC12 CELLS - DIFFERENTIATION PARALLELS AN INCREASE IN PKC BETA(II)

被引:73
作者
WOOTEN, MW
SEIBENHENER, ML
SOH, Y
EWALD, SJ
WHITE, KR
LLOYD, ED
OLIVIER, A
PARKER, PJ
机构
[1] AUBURN UNIV,ALABAMA AGR EXPT STN,DEPT CHEM,AUBURN,AL 36849
[2] AUBURN UNIV,ALABAMA AGR EXPT STN,DEPT POULTRY SCI,AUBURN,AL 36849
[3] AUBURN UNIV,ALABAMA AGR EXPT STN,DEPT PATHOBIOL,AUBURN,AL 36849
[4] IMPERIAL CANC RES FUND,PROT PHOSPHORYLAT LAB,LONDON WC2A 3PX,ENGLAND
关键词
PROTEIN KINASE-C; ISOFORM; DIFFERENTIATION; NERVE GROWTH FACTOR; PC12;
D O I
10.1016/0014-5793(92)80025-C
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
Nerve growth factor (NGF) treatment of PC12 cells induced a 2.8-fold increase in protein kinase C activity concomitant with differentiation and acquisition of neurites. PKC protein isoforms were separated by sequential chromatography on DEAE-Sephacel/hydroxylapatite. A broad peak of PKC activity eluted which corresponded to the alpha PKC isoform. In control cells, message for all six PKC isoforms was detected and expressed as epsilon > zeta = gamma > delta > beta > alpha. Western blot of whole cell lysates revealed a large increase in the beta(II), while slight changes were observed for the other five PKC isoforms during treatment (1-14 days) with HGF (50 ng/ml). In parallel, coordinate changes in the expression of the individual transcripts for the six isoforms occurred during NGF treatment. Induction and accumulation of PKC beta(II) may play a role in maintenance of neuronal morphology.
引用
收藏
页码:74 / 78
页数:5
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