Connexin 43 confers resistance to hydrogen peroxide-mediated apoptosis

被引:59
作者
Giardina, Sarah F. [1 ]
Mikami, Maya [1 ]
Goubaeva, Farida [1 ]
Yang, Jay [1 ]
机构
[1] Columbia Univ Coll Phys & Surg, Dept Anesthesiol, New York, NY 10032 USA
关键词
connexin; 43; apoptosis; C6; glioma; primary astrocytes; siRNA knockdown; hydrogen peroxide; apoptosis signal-regulating kinase I;
D O I
10.1016/j.bbrc.2007.08.066
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The current study aimed to understand the anti-apoptotic effect of overexpressed gap junction forming protein connexin (Cx) 43 in C6 glioma cells. C6 cells exposed to hydrogen peroxide (H2O2) or staurosporine demonstrated morphological and biochemical changes consistent with apoptosis, whereas C6 cells expressing Cx43 demonstrated relative resistance to H2O2, but not to staurosporine. This selective protection against H2O2 was due to inhibition of caspase-3 activation in Cx43 expressing cells. siRNA knockdown experiments in rat primary astrocytes confirmed the presence of endogenous Cx43-mediated anti-apoptotic effect. Cx43 interacts with the upstream apoptosis signal-regulating kinase I known to mediate H2O2-induced apoptosis providing a possible mechanism for protection. These findings provided new evidence for regulation of the mitogen activated protein kinase pathway and apoptosis by Cx43 implicating this protein in intracellular signaling beyond its role as a gap junction forming protein on the plasma membrane. (c) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:747 / 752
页数:6
相关论文
共 24 条
[1]   Transfer of biologically important molecules between cells through gap junction channels [J].
Alexander, DB ;
Goldberg, GS .
CURRENT MEDICINAL CHEMISTRY, 2003, 10 (19) :2045-2058
[2]   Gap junctions: the "kiss of death" and the "kiss of life" [J].
Andrade-Rozental, AF ;
Rozental, R ;
Hopperstad, MG ;
Wu, JK ;
Vrionis, FD ;
Spray, DC .
BRAIN RESEARCH REVIEWS, 2000, 32 (01) :308-315
[3]   Protein kinase C-α and -ε modulate connexin-43 phosphorylation in human heart [J].
Bowling, N ;
Huang, XD ;
Sandusky, GE ;
Fouts, RL ;
Mintze, K ;
Esterman, M ;
Allen, PD ;
Maddi, R ;
McCall, E ;
Vlahos, CJ .
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 2001, 33 (04) :789-798
[4]   Clustering of connexin 43-enhanced green fluorescent protein gap junction channels and functional coupling in living cells [J].
Bukauskas, FF ;
Jordan, K ;
Bukauskiene, A ;
Bennett, MVL ;
Lampe, PD ;
Laird, DW ;
Verselis, VK .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (06) :2556-2561
[5]   Regulation of epidermal growth factor-induced connexin 43 gap junction communication by big mitogen-activated protein kinase 1/ERK5 but not ERK1/2 kinase activation [J].
Cameron, SJ ;
Malik, S ;
Akaike, M ;
Lerner-Marmarosh, N ;
Yan, C ;
Lee, JD ;
Abe, J ;
Yang, J .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (20) :18682-18688
[6]   Activation of apoptosis signal regulating kinase 1 (ASK1) by the adapter protein Daxx [J].
Chang, HY ;
Nishitoh, H ;
Yang, XL ;
Ichijo, H ;
Baltimore, D .
SCIENCE, 1998, 281 (5384) :1860-1863
[7]   The ε subtype of protein kinase C is required for cardiomyocyte connexin-43 phosphorylation [J].
Doble, BW ;
Ping, PP ;
Kardami, E .
CIRCULATION RESEARCH, 2000, 86 (03) :293-301
[8]   Proliferation, differentiation and apoptosis in connexin43-null osteoblasts [J].
Furlan, F ;
Lecanda, F ;
Screen, J ;
Civitelli, R .
CELL COMMUNICATION AND ADHESION, 2001, 8 (4-6) :367-371
[9]   Multicolor and electron microscopic imaging of connexin trafficking [J].
Gaietta, G ;
Deerinck, TJ ;
Adams, SR ;
Bouwer, J ;
Tour, O ;
Laird, DW ;
Sosinsky, GE ;
Tsien, RY ;
Ellisman, MH .
SCIENCE, 2002, 296 (5567) :503-507
[10]   Array analysis of gene expression in connexin-43 null astrocytes [J].
Iacobas, DA ;
Maldonado, MU ;
Iacobas, S ;
Scemes, E ;
Spray, DC .
PHYSIOLOGICAL GENOMICS, 2003, 15 (03) :177-190