Regulation of Bcl-xl channel activity by calcium

被引:47
作者
Lam, M
Bhat, MB
Nuñez, G
Ma, JJ
Distelhorst, CW
机构
[1] Case Western Reserve Univ, Dept Physiol & Biophys, Cleveland, OH 44106 USA
[2] Case Western Reserve Univ, Dept Med, Cleveland, OH 44106 USA
[3] Case Western Reserve Univ, Dept Pharmacol, Cleveland, OH 44106 USA
[4] Univ Michigan, Sch Med, Dept Pathol, Ann Arbor, MI 48109 USA
关键词
D O I
10.1074/jbc.273.28.17307
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
Recent studies have demonstrated that the anti-apoptotic proteins, Bcl-2 and Bcl-xl, with the carboxyl terminal hydrophobic domain removed, form cation-selective channels in the lipid bilayer reconstitution system. However, the regulatory properties of these channels are unknown. In this study, we investigated the ion-conducting properties of full length Bcl-xl in the lipid bilayer reconstitution system. Our findings indicate that Bcl-xl forms a cation-selective channel that conducts sodium but not calcium and that Bcl-xl channel activity is reversibly inhibited by luminal calcium with a half-dissociation constant of similar to 60 mu M This calcium-de pendent regulation of the Bcl-xl channel provides new insights into the roles of calcium and Bcl-2-related proteins in the programmed cell death pathway.
引用
收藏
页码:17307 / 17310
页数:4
相关论文
共 35 条
[21]   MEASUREMENT OF MITOCHONDRIAL FREE CA2+ CONCENTRATION IN LIVING SINGLE-RAT CARDIAC MYOCYTES [J].
MIYATA, H ;
SILVERMAN, HS ;
SOLLOTT, SJ ;
LAKATTA, EG ;
STERN, MD ;
HANSFORD, RG .
AMERICAN JOURNAL OF PHYSIOLOGY, 1991, 261 (04) :H1123-H1134
[22]   Fluorescent indicators for Ca2+ based on green fluorescent proteins and calmodulin [J].
Miyawaki, A ;
Llopis, J ;
Heim, R ;
McCaffery, JM ;
Adams, JA ;
Ikura, M ;
Tsien, RY .
NATURE, 1997, 388 (6645) :882-887
[23]   X-ray and NMR structure of human Bcl-x(L), an inhibitor of programmed cell death [J].
Muchmore, SW ;
Sattler, M ;
Liang, H ;
Meadows, RP ;
Harlan, JE ;
Yoon, HS ;
Nettesheim, D ;
Chang, BS ;
Thompson, CB ;
Wong, SL ;
Ng, SC ;
Fesik, SW .
NATURE, 1996, 381 (6580) :335-341
[24]   Bcl-2 potentiates the maximal calcium uptake capacity of neural cell mitochondria [J].
Murphy, AN ;
Bredesen, DE ;
Cortopassi, G ;
Wang, E ;
Fiskum, G .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (18) :9893-9898
[25]  
NGUYEN M, 1993, J BIOL CHEM, V268, P25265
[26]   BCL-2 HETERODIMERIZES IN-VIVO WITH A CONSERVED HOMOLOG, BAX, THAT ACCELERATES PROGRAMMED CELL-DEATH [J].
OLTVAI, ZN ;
MILLIMAN, CL ;
KORSMEYER, SJ .
CELL, 1993, 74 (04) :609-619
[27]   Double identity for proteins of the Bcl-2 family [J].
Reed, JC .
NATURE, 1997, 387 (6635) :773-776
[28]   Channel formation by antiapoptotic protein Bcl-2 [J].
Schendel, SL ;
Xie, ZH ;
Montal, MO ;
Matsuyama, S ;
Montal, M ;
Reed, JC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (10) :5113-5118
[29]   Comparison of the ion channel characteristics of proapoptotic BAX and antiapoptotic BCL-2 [J].
Schlesinger, PH ;
Gross, A ;
Yin, XM ;
Yamamoto, K ;
Saito, M ;
Waksman, G ;
Korsmeyer, SJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (21) :11357-11362
[30]   Bcl-2 prevents apoptotic mitochondrial dysfunction by regulating proton flux [J].
Shimizu, S ;
Eguchi, Y ;
Kamiike, W ;
Funahashi, Y ;
Mignon, A ;
Lacronique, V ;
Matsuda, H ;
Tsujimoto, Y .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (04) :1455-1459