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;
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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.
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页码:281 / 287
页数:6
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