Differential redistribution of protein kinase C isoforms by cyclic AMP in HL60 cells

被引:14
作者
Miguel, BG
Calcerrada, MC
Mata, F
Aller, P
Clemente, R
Catalán, RE
Martínez, AM
机构
[1] Univ Autonoma Madrid, CSIC, Ctr Biol Mol Severo Ochoa, Dept Mol Biol, E-28049 Madrid, Spain
[2] Univ Complutense Madrid, Fac Biol, Dept Bioquim & Biol Mol 1, E-28040 Madrid, Spain
[3] CSIC, Ctr Invest Biol, E-28006 Madrid, Spain
关键词
protein kinase C isoforms; translocation; nucleus; cultured promyelocytic HL60 cells;
D O I
10.1006/bbrc.2000.3194
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
In this study we have analyzed the distribution of protein kinase C isoforms in cytosol, membrane, and nucleus in HL60 cells. Furthermore, we have studied the redistribution of these isoforms after cyclic AMP treatment. Protein kinase C localization and cyclic AMP-induced translocation was demonstrated by Western blot analysis. Cytosol, membrane and nucleus in HL60 cells expressed the abundance of protein kinase C alpha, beta I, beta II, delta, lambda, and zeta isoforms. After cyclic AMP treatment, the amount of protein kinase C beta I and zeta increased only in the nucleus, while protein kinase C delta increased in the three fractions tested. These effects were dependent on the cyclic AMP concentration and duration of action. Our results suggest the existence of cross-talk between the cyclic AMP system and protein kinase C in HL60 cells. Taking into account the processes regulated by protein kinase C, these findings also suggest that cyclic AMP plays a regulatory role in various cellular responses in HL60 cells, such as differentiation and gene expression. The increase observed in PRC delta was due to cyclic AMP-dependent protein kinase C activation, and the synthesis of enzyme was probably activated by the nucleotide, (C) 2000 Academic Press.
引用
收藏
页码:596 / 602
页数:7
相关论文
共 38 条
[21]  
LOZANO J, 1994, J BIOL CHEM, V269, P19200
[22]  
MACFARLANE DE, 1994, J BIOL CHEM, V269, P4327
[23]  
MAKOWSKE M, 1988, J BIOL CHEM, V263, P3402
[24]  
Martelli AM, 1999, J CELL BIOCHEM, V74, P499, DOI 10.1002/(SICI)1097-4644(19990915)74:4<499::AID-JCB1>3.3.CO
[25]  
2-O
[26]  
MASMOUDI A, 1989, J BIOL CHEM, V264, P1172
[27]   INTRACELLULAR SIGNALING BY HYDROLYSIS OF PHOSPHOLIPIDS AND ACTIVATION OF PROTEIN-KINASE-C [J].
NISHIZUKA, Y .
SCIENCE, 1992, 258 (5082) :607-614
[28]   PROTEIN KINASES .5. PROTEIN-KINASE-C AND LIPID SIGNALING FOR SUSTAINED CELLULAR-RESPONSES [J].
NISHIZUKA, Y .
FASEB JOURNAL, 1995, 9 (07) :484-496
[29]  
OLSON EN, 1993, CELL GROWTH DIFFER, V4, P699
[30]   THE CATALYTIC SUBUNIT OF CAMP-DEPENDENT PROTEIN-KINASE INDUCES EXPRESSION OF GENES CONTAINING CAMP-RESPONSIVE ENHANCER ELEMENTS [J].
RIABOWOL, KT ;
FINK, JS ;
GILMAN, MZ ;
WALSH, DA ;
GOODMAN, RH ;
FERAMISCO, JR .
NATURE, 1988, 336 (6194) :83-86