Mitochondrial anomalies are associated with the induction of intrinsic cell death proteins-BCl2, Bax, cytochrome-c and p53 in mice brain during experimental fatal murine cerebral malaria

被引:22
作者
Kumar, KA [1 ]
Babu, PP [1 ]
机构
[1] Univ Hyderabad, Sch Life Sci, Dept Anim Sci, Hyderabad 500046, Andhra Pradesh, India
关键词
apoptosis; Bcl(2); Bax; cytochrome-c; cytokines; cerebral malaria; mitochondria; p53;
D O I
10.1016/S0304-3940(02)00470-6
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The levels of apoptosis associated proteins Bcl(2), Bax, cytochrome-c and p53 was investigated in mice cerebral cortex and cerebellum, using an experimental model of fatal murine cerebral malaria (FMCM). Owing to the activation of events central to mitochondrial dysfunctions, we monitored the structural integrity of mitochondria in cerebral malaria (CM) infected brain tissue by transmission EM (TEM) studies. Western blot analysis revealed the induction of Bcl(2), Bax, cytochrome-c and p53 in both cortex and cerebellum. The TEM studies revealed extensive vacuolation and swelling of mitochondria in infected brain suggestive of a late stage of degeneration. Our results underscore the activation of an intrinsic cell death pathway as evinced by the induction of mitochondria associated apoptotic proteins Bcl(2), Bax and cytochrome-c and further envisages the induction of p53 as a possible continuation of the post receptor signaling events associated with tumor necrosis factor induction following inflammatory responses during CM. These findings may be crucial to mitochondrial dysfunctions underlying the pathology of FMCM. (C) 2002 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:319 / 323
页数:5
相关论文
共 24 条
[1]   Inhibition of Bax channel-forming activity by Bcl-2 [J].
Antonsson, B ;
Conti, F ;
Ciavatta, A ;
Montessuit, S ;
Lewis, S ;
Martinou, I ;
Bernasconi, L ;
Bernard, A ;
Mermod, JJ ;
Mazzei, G ;
Maundrell, K ;
Gambale, F ;
Sadoul, R ;
Martinou, JC .
SCIENCE, 1997, 277 (5324) :370-372
[2]  
Chresta CM, 1996, CANCER RES, V56, P1834
[3]   Bax-induced caspase activation and apoptosis via cytochrome c release from mitochondria is inhibitable by Bcl-xL [J].
Finucane, DM ;
Bossy-Wetzel, E ;
Waterhouse, NJ ;
Cotter, TG ;
Green, DR .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (04) :2225-2233
[4]  
Foo SY, 1999, TRENDS GENET, V15, P229
[5]  
GARETH T, 1997, BRAIN PATHOL, V7, P569
[6]   TUMOR-NECROSIS-FACTOR (CACHECTIN) AS AN ESSENTIAL MEDIATOR IN MURINE CEREBRAL MALARIA [J].
GRAU, GE ;
FAJARDO, LF ;
PIGUET, PF ;
ALLET, B ;
LAMBERT, PH ;
VASSALLI, P .
SCIENCE, 1987, 237 (4819) :1210-1212
[7]  
GRAU GE, 1986, J IMMUNOL, V137, P1348
[8]   Enforced dimerization of BAX results in its translocation, mitochondrial dysfunction and apoptosis [J].
Gross, A ;
Jockel, J ;
Wei, MC ;
Korsmeyer, SJ .
EMBO JOURNAL, 1998, 17 (14) :3878-3885
[9]   Bax directly induces release of cytochrome c from isolated mitochondria [J].
Jürgensmeier, JM ;
Xie, ZH ;
Deveraux, Q ;
Ellerby, L ;
Bredesen, D ;
Reed, JC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (09) :4997-5002
[10]  
Kim CN, 1997, CANCER RES, V57, P3115