A secreted caspase-3-substrate-cleaving activity at low pH belongs to cathepsin B: a study on primary brain cell cultures

被引:0
作者
M. V. Onufriev
A. A. Yakovlev
A. A. Lyzhin
M. Yu. Stepanichev
L. G. Khaspekov
N. V. Gulyaeva
机构
[1] Russian Academy of Sciences,Institute of Higher Nervous Activity and Neurophysiology
[2] Russian Academy of Sciences,Institute of Theoretical and Experimental Biophysics
[3] Russian Academy of Medical Sciences,Neurology Research Center
来源
Biochemistry (Moscow) | 2009年 / 74卷
关键词
cathepsin B; caspase-3; ischemia/reoxygenation; neurons; glia;
D O I
暂无
中图分类号
学科分类号
摘要
The cysteine proteases caspase-3 and cathepsins are involved in both neuronal plasticity and neuropathology. Using primary neuroglial and glial cerebellar cultures, the pH dependence of cleavage of a synthetic caspase-3 substrate, Ac-DEVD-AMC, was studied. At acidic pH, cathepsin B cleaved Ac-DEVD, this activity being significantly higher than that of caspase-3 at pH 7.4. This activity is blocked by peptide inhibitors of both caspase-3 and cathepsin B. Substitution of culture medium for balanced salt solution stimulated cathepsin B secretion in both types of cultures. Ischemia (oxygen-glucose deprivation) significantly decreased secretion of cathepsin B activities into the culture medium.
引用
收藏
页码:281 / 287
页数:6
相关论文
共 186 条
[1]  
Turk B.(1997)undefined Biol. Chem. 378 141-150
[2]  
Turk V.(2000)undefined Prog. Neurobiol. 62 273-295
[3]  
Turk D.(2003)undefined J. Exp. Med. 197 1323-1334
[4]  
Yamashima T.(2004)undefined J. Cerebr. Blood Flow Metab. 24 1272-1279
[5]  
Boya P.(2001)undefined J. Neurochem. 76 1475-1484
[6]  
Andreau K.(2005)undefined J. Neurochem. 92 1228-1242
[7]  
Poncet D.(1994)undefined Cell 78 761-771
[8]  
Zamzani N.(2004)undefined J. Cerebr. Blood Flow Metab. 24 1119-1132
[9]  
Perfettini J. L.(1998)undefined Cell Death Differ. 5 1051-1061
[10]  
Metivier D.(2001)undefined J. Biol. Chem. 276 32750-32755