Changes in mitochondrial surface charge mediate recruitment of signaling molecules during apoptosis

被引:34
作者
Heit, Bryan [1 ]
Yeung, Tony [1 ]
Grinstein, Sergio [1 ]
机构
[1] Hosp Sick Children, Cell Biol Programme, Toronto, ON M5G 1X8, Canada
来源
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY | 2011年 / 300卷 / 01期
关键词
mitochondria; electrostatic; cardiolipin; lipids; CYTOCHROME-C RELEASE; 10-N-NONYL ACRIDINE-ORANGE; CARDIOLIPIN-BINDING DOMAIN; CONTACT SITES; CELLS; MEMBRANE; LOCALIZATION; PHAGOCYTOSIS; PLATELETS; PROTEINS;
D O I
10.1152/ajpcell.00139.2010
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Heit B, Yeung T, Grinstein S. Changes in mitochondrial surface charge mediate recruitment of signalling molecules during apoptosis. Am J Physiol Cell Physiol 300: C33-C41, 2011. First published October 6, 2010; doi: 10.1152/ajpcell.00139.2010.-Electrostatic interactions with negative lipids contribute to the subcellular localization of polycationic proteins. In situ measurements using cytosolic probes of surface charge indicate that normal mitochondria are not noticeably electronegative. However, during apoptosis mitochondria accrue negative charge and acquire the ability to attract cationic proteins, including K-Ras. The marked increase in the surface charge of mitochondria occurs early in apoptosis, preceding depolarization of their inner membrane, cytochrome c release, and flipping of phosphatidylserine across the plasmalemma. Using novel biosensors, we determined that the increased electronegativity of the mitochondria coincided with and was likely attributable to increased exposure of cardiolipin, which is dianionic. Ectopic (over) expression of cardiolipin-binding proteins precluded the increase in surface charge and inhibited apoptosis, implying that mitochondrial exposure of negatively charged lipids is required for progression of programmed cell death.
引用
收藏
页码:C33 / C41
页数:9
相关论文
共 37 条
[1]  
ARDAIL D, 1990, J BIOL CHEM, V265, P18797
[2]   PKC regulates a farnesyl-electrostatic switch on K-Ras that promotes its association with Bcl-XL on mitochondria and induces apoptosis [J].
Bivona, TG ;
Quatela, SE ;
Bodemann, BO ;
Ahearn, IM ;
Soskis, MJ ;
Mor, A ;
Miura, J ;
Wiener, HH ;
Wright, L ;
Saba, SG ;
Yim, D ;
Fein, A ;
Perez de Castro, I ;
Li, C ;
Thompson, CB ;
Cox, AD ;
Philips, MR .
MOLECULAR CELL, 2006, 21 (04) :481-493
[3]   IDENTIFICATION AND PRIMARY STRUCTURE OF THE CARDIOLIPIN-BINDING DOMAIN OF MITOCHONDRIAL CREATINE-KINASE [J].
CHENEVAL, D ;
CARAFOLI, E .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1988, 171 (1-2) :1-9
[4]   THE DEPENDENCE ON CA2+ OF PHOSPHATIDYLINOSITOL BREAKDOWN AND ENZYME-SECRETION IN RABBIT NEUTROPHILS STIMULATED BY FORMYLMETHIONYLLEUCYLPHENYLALANINE OR IONOMYCIN [J].
COCKCROFT, S ;
BENNETT, JP ;
GOMPERTS, BD .
BIOCHEMICAL JOURNAL, 1981, 200 (03) :501-508
[5]   Location of the myristoylated alanine-rich C-kinase substrate (MARCKS) effector domain in negatively charged phospholipid bicelles [J].
Ellena, JF ;
Burnitz, MC ;
Cafiso, DS .
BIOPHYSICAL JOURNAL, 2003, 85 (04) :2442-2448
[6]   Cardiolipin clusters and membrane domain formation induced by mitochondrial proteins [J].
Epand, Raquel F. ;
Tokarska-Schlattner, Malgorzata ;
Schlattner, Uwe ;
Wallimann, Theo ;
Epand, Richard M. .
JOURNAL OF MOLECULAR BIOLOGY, 2007, 365 (04) :968-980
[7]  
Fernandez MG, 2002, CELL GROWTH DIFFER, V13, P449
[8]   Do mitochondria act as "Cargo boats" in the journey of GD3 to the nucleus during apoptosis? [J].
Garofaloa, Tina ;
Tinari, Antonella ;
Matarrese, Paola ;
Giammarioli, Anna Maria ;
Manganelli, Valeria ;
Ciarlo, Laura ;
Misasi, Roberta ;
Sorice, Maurizio ;
Malorni, Walter .
FEBS LETTERS, 2007, 581 (21) :3899-3903
[9]   Binding of 10-N-nonyl acridine orange to cardiolipin-deficient yeast cells:: Implications for assay of cardiolipin [J].
Gohil, VM ;
Gvozdenovic-Jeremic, J ;
Schlame, M ;
Greenberg, ML .
ANALYTICAL BIOCHEMISTRY, 2005, 343 (02) :350-352
[10]   Cardiolipin provides an essential activating platform for caspase-8 on mitochondria [J].
Gonzalvez, Francois ;
Schug, Zachary T. ;
Houtkooper, Riekelt H. ;
MacKenzie, Elaine D. ;
Brooks, David G. ;
Wanders, Ronald J. A. ;
Petit, Patrice X. ;
Vaz, Frederic M. ;
Gottlieb, Eyal .
JOURNAL OF CELL BIOLOGY, 2008, 183 (04) :681-696