Mitochondria are the primary source of the H2O2 signal for glucocorticoid-induced apoptosis of lymphoma cells

被引:20
作者
Tome, Margaret E. [1 ]
Lee, Kristy [1 ]
Jaramillo, Melba C. [1 ]
Briehl, Margaret M. [1 ]
机构
[1] Univ Arizona, Dept Pathol, Tucson, AZ 85724 USA
关键词
apoptosis; lymphoma mitochondria; reactive oxygen species; HYDROGEN-PEROXIDE; CYTOCHROME-C; RESPIRATORY-CHAIN; ACTIVATION; LIPOXYGENASE; INHIBITION; THYMOCYTES; RECEPTOR; RELEASE; GLUCOSE;
D O I
10.3892/etm.2012.595
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Glucocorticoids are a class of steroid hormones commonly used for the treatment of hematological malignancies due to their ability to induce apoptosis in lymphoid cells. An understanding of the critical steps in glucocorticoid-induced apoptosis is required to identify sources of drug resistance. Previously, we found that an increase in hydrogen peroxide is a necessary signal for glucocorticoid-induced apoptosis. In the current study, we found that mitochondria are the source of the signal. Glucocorticoid treatment inhibited Complex I and Complex III of the electron transport chain (ETC). Mitochondrial matrix reactive oxygen species (ROS) increased concomitantly with the oxidation of the mitochondrial glutathione pool. Treatment with Tiron, a superoxide scavenger, inhibited the signal. This suggests that the hydrogen peroxide signal originates as superoxide from the mitochondria and is metabolized to hydrogen peroxide. An inability to generate mitochondrial oxidants in response to glucocorticoids could cause drug resistance.
引用
收藏
页码:237 / 242
页数:6
相关论文
共 31 条
[1]   METABOLIC ALTERATIONS ASSOCIATED WITH PROLIFERATION OF MITOGEN-ACTIVATED LYMPHOCYTES AND OF LYMPHOBLASTOID CELL-LINES - EVALUATION OF GLUCOSE AND GLUTAMINE-METABOLISM [J].
BRAND, K ;
LEIBOLD, W ;
LUPPA, P ;
SCHOERNER, C ;
SCHULZ, A .
IMMUNOBIOLOGY, 1986, 173 (01) :23-34
[2]   Dexamethasone-induced thymocyte apoptosis: Apoptotic signal involves the sequential activation of phosphoinositide-specific phospholipase C, acidic sphingomyelinase, and caspases [J].
Cifone, MG ;
Migliorati, G ;
Parroni, R ;
Marchetti, C ;
Millimaggi, D ;
Santoni, A ;
Riccardi, C .
BLOOD, 1999, 93 (07) :2282-2296
[3]   Reactive oxygen species, cellular redox systems, and apoptosis [J].
Circu, Magdalena L. ;
Aw, Tak Yee .
FREE RADICAL BIOLOGY AND MEDICINE, 2010, 48 (06) :749-762
[4]   Recent insights into the mechanism of glucocorticosteroid-induced apoptosis [J].
Distelhorst, CW .
CELL DEATH AND DIFFERENTIATION, 2002, 9 (01) :6-19
[5]   Electron transfer between cytochrome c and p66Shc generates reactive oxygen species that trigger mitochondrial apoptosis [J].
Giorgio, M ;
Migliaccio, E ;
Orsini, F ;
Paolucci, D ;
Moroni, M ;
Contursi, C ;
Pelliccia, G ;
Luzi, L ;
Minucci, S ;
Marcaccio, M ;
Pinton, P ;
Rizzuto, R ;
Bernardi, P ;
Paolucci, F ;
Pelicci, PG .
CELL, 2005, 122 (02) :221-233
[6]   Investigating mitochondrial redox potential with redox-sensitive green fluorescent protein indicators [J].
Hanson, GT ;
Aggeler, R ;
Oglesbee, D ;
Cannon, M ;
Capaldi, RA ;
Tsien, RY ;
Remington, SJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (13) :13044-13053
[7]  
HARRIS AW, 1973, J IMMUNOL, V110, P431
[8]   The biochemistry of apoptosis [J].
Hengartner, MO .
NATURE, 2000, 407 (6805) :770-776
[9]   Glucocorticoids in T cell apoptosis and function [J].
Herold, MJ ;
McPherson, KG ;
Reichardt, HM .
CELLULAR AND MOLECULAR LIFE SCIENCES, 2006, 63 (01) :60-72
[10]   Crosstalk pathway for inhibition of glucocorticoid-induced apoptosis by T cell receptor signaling [J].
Jamieson, CAM ;
Yamamoto, KR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (13) :7319-7324