Calpain-μ is activated in hepatocyte mitochondria during ischemia-reperfusion injury.

被引:3
作者
Miyoshi, H
Sakon, M
Umeshita, K
Eguchi, H
Kishimoto, S
Dono, K
Gotoh, M
Imajoh-Ohmi, S
Monden, M
机构
[1] Osaka Univ, Sch Med, Dept Surg 2, Suita, Osaka 565, Japan
[2] Univ Tokyo, Inst Med Sci, Tokyo, Japan
关键词
ischemia-reperfusion; liver; calpain-mu activation; mitochondria;
D O I
10.1016/S1386-6346(97)00111-3
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Mitochondrial permeability transition (MMPT), a rapid increase in the permeability of the inner mitochondrial membrane to low molecular weight solutes, plays a predominant role in ischemia-reperfusion injury of hepatocytes. Calpain, a Ca2+-dependent neutral proteinase (EC 3, 4, 22, 17) has been considered to be involved in the induction of MMPT, but its activation in mitochondria remains to be proven. By immunoelectron microscopic study with antibodies that specifically recognize the pro-enzyme and intermediate (activated) forms of calpain-mu, its activation at mitochondria was investigated in a 15-min ischemia model of rat liver. Activated calpain-mu was not detected in hepatocytes before ischemia, but was observed primarily in mitochondria 15 min after reperfusion. In contrast, the pro-enzyme form of calpain-mu was detected equally throughout the cytoplasm before ischemia, and no significant change was observed after reperfusion. This data provides the direct evidence that calpain-mu was activated in mitochondria during the ischemia-reperfusion injury of the liver. (C) 1998 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:255 / 259
页数:5
相关论文
共 10 条
[1]   Induction of the mitochondrial permeability transition by protease activity in rats: A mechanism of hepatocyte necrosis [J].
Aguilar, HI ;
Botla, R ;
Arora, AS ;
Bronk, SF ;
Gores, GJ .
GASTROENTEROLOGY, 1996, 110 (02) :558-566
[2]   CALCIUM-ACTIVATED PROTEOLYTIC ACTIVITY IN RAT-LIVER MITOCHONDRIA [J].
BEER, DG ;
HJELLE, JJ ;
PETERSEN, DR ;
MALKINSON, AM .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1982, 109 (04) :1276-1283
[3]   Calpain activation in plasma membrane bleb formation during tert-butyl hydroperoxide-induced rat hepatocyte injury [J].
Miyoshi, H ;
Umeshita, K ;
Sakon, M ;
ImajohOhmi, S ;
Fujitani, K ;
Gotoh, M ;
Oiki, E ;
Kambayashi, J ;
Monden, M .
GASTROENTEROLOGY, 1996, 110 (06) :1897-1904
[4]  
MURATA M, 1994, HEPATOLOGY, V19, P1223, DOI 10.1016/0270-9139(94)90870-2
[5]   PEROXYNITRITE FORMED BY SIMULTANEOUS NITRIC-OXIDE AND SUPEROXIDE GENERATION CAUSES CYCLOSPORINE-A-SENSITIVE MITOCHONDRIAL CALCIUM EFFLUX AND DEPOLARIZATION [J].
PACKER, MA ;
MURPHY, MP .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1995, 234 (01) :231-239
[6]   LIVER-CELL NECROSIS - CELLULAR MECHANISMS AND CLINICAL IMPLICATIONS [J].
ROSSER, BG ;
GORES, GJ .
GASTROENTEROLOGY, 1995, 108 (01) :252-275
[7]   CALPAIN - NEW PERSPECTIVES IN MOLECULAR DIVERSITY AND PHYSIOLOGICAL-PATHOLOGICAL INVOLVEMENT [J].
SAIDO, TC ;
SORIMACHI, H ;
SUZUKI, K .
FASEB JOURNAL, 1994, 8 (11) :814-822
[8]   INTERACTIONS OF ADRIAMYCIN AGLYCONES WITH MITOCHONDRIA MAY MEDIATE ADRIAMYCIN CARDIOTOXICITY [J].
SOKOLOVE, PM .
INTERNATIONAL JOURNAL OF BIOCHEMISTRY, 1994, 26 (12) :1341-1350
[9]  
TAVARES A, 1991, BIOMED BIOCHIM ACTA, V50, P523
[10]   CALPAIN INHIBITION - AN OVERVIEW OF ITS THERAPEUTIC POTENTIAL [J].
WANG, KKW ;
YUEN, PW .
TRENDS IN PHARMACOLOGICAL SCIENCES, 1994, 15 (11) :412-419