Protein kinase Cα is a calpain target in cultured embryonic muscle cells

被引:0
作者
B. Aragon
S. Poussard
S. Dulong
K. Touyarot
E. Dargelos
J.J. Brustis
D. Levieux
A. Ducastaing
P. Cottin
机构
来源
Molecular and Cellular Biochemistry | 2002年 / 231卷
关键词
protein kinase C; calpains; myogenesis; phorbol myristate acetate; down-regulation;
D O I
暂无
中图分类号
学科分类号
摘要
Previously we isolated a μ-calpain/PKCα complex from skeletal muscle which suggested tight interactions between the Ca2+-dependent protease and the kinase in this tissue. Our previous studies also underlined the involvement of ubiquitous calpains in muscular fusion and differentiation. In order to precise the relationships between PKCα and ubiquitous calpains in muscle cells, the expression of these two enzymes was first examined during myogenesis of embryonic myoblasts in culture.
引用
收藏
页码:97 / 106
页数:9
相关论文
共 349 条
[1]  
Huang Y(2001)The calpain family and human disease Trends Mol Med 7 355-361
[2]  
Wang KKW(1998)Calpain: A protease in search of a function? Biochem Biophys Res Commun 247 193-203
[3]  
Carafoli E(1991)Calcium-activated neutral protease (calpain) system: Structure, function and regulation Physiol Rev 71 813-847
[4]  
Molinari M(1997)Evidence for participation of a calpain-like cysteine protease in cell cycle progression through late G1 phase Biochem Biophys Res Comm 236 555-558
[5]  
Croall DE(1998)A novel aspect of calpain activation FEBS Lett 433 1-4
[6]  
Demartino GN(1995)Mutation in the proteolytic enzyme calpain 3 cause limb-girdle muscular dystrophy type 2A Cell 81 27-40
[7]  
Mellgren RL(2000)Genetic variation in the gene encoding calpain-10 is associated with type 2 diabetes mellitus Nat Genet 26 163-175
[8]  
Suzuki K(1992)Intracellular signalling by hydrolysis phospholipids and activation of protein kinase C Science 258 607-614
[9]  
Sorimachi H(1996)Protein kinase C and its substrates Mol Cell Endocrinol 116 1-29
[10]  
Richard I(1988)The structure expression and properties of additional members of the protein kinase C family J Biol Chem 263 6927-6932