Mitochondrial lipid alterations during Fas- and radiation-induced apoptosis

被引:58
作者
Matsko, CM
Hunter, OC
Rabinowich, H
Lotze, MT
Amoscato, AA [1 ]
机构
[1] Univ Pittsburgh, Ctr Biotechnol & Bioengn, Mass Spectrometry Fac, Pittsburgh, PA 15219 USA
[2] Univ Pittsburgh, Sch Med, Dept Pathol, Pittsburgh, PA 15261 USA
[3] Univ Pittsburgh, Sch Med, Dept Surg, Pittsburgh, PA 15261 USA
[4] Univ Pittsburgh, Inst Canc, Pittsburgh, PA 15213 USA
关键词
phosphatidylglycerol; cardiolipin; ceramide; mitochondria; apoptosis;
D O I
10.1006/bbrc.2001.5696
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
In the present study, we investigated the dynamic alterations in mitochondrial lipids occurring during Fas- and radiation-induced cell death. Cross-linking of CD-95 on Fas-sensitive Jurkat cells produced rapid increases in two species of mitochondrial phosphatidylglycerol. By 2.5 h, phosphatidylglycerol decreases below basal levels, concomitant with an increase in mitochondrial ceramide. In addition, between 1.5 and 3.0 h after anti-Fas crosslinking, there is a continued loss of mitochondrial cardiolipin. When gamma irradiation was used to induce apoptosis, similar lipid changes occurred, although with somewhat slower kinetics. Fas-resistant Jurkat cells exhibited phosphatidylglycerol as the dominant lipid species in their mitochondria. Following Fas ligation, there is a transient decrease in phosphatidylglycerol, but cardiolipin and ceramide remained unchanged. The high basal levels of PG in Fas-resistant cells and the increase in PG levels in Fas-sensitive cells undergoing apoptosis was determined to be due to increased PGP synthase activity. Thus, critical mitochondrial lipids could potentially serve as novel targets in regulating the apoptotic process. (C) 2001 Academic Press.
引用
收藏
页码:1112 / 1120
页数:9
相关论文
共 55 条
[1]  
AVE K, 1983, J BIOL CHEM, V258, P11793
[2]   RESOLUTION OF GRANULES FROM RABBIT HETEROPHIL LEUKOCYTES INTO DISTINCT POPULATIONS BY ZONAL SEDIMENTATION [J].
BAGGIOLINI, M ;
HIRSCH, JG ;
DEDUVE, C .
JOURNAL OF CELL BIOLOGY, 1969, 40 (02) :529-+
[3]  
Banki K, 1999, J IMMUNOL, V162, P1466
[4]   TISSUE FRACTIONATION STUDIES .17. INTRACELLULAR DISTRIBUTION OF MONOAMINE OXIDASE ASPARTATE AMINOTRANSFERASE ALANINE AMINOTRANSFERASE D-AMINO ACID OXIDASE + CATALASE IN RAT-LIVER TISSUE [J].
BAUDHUIN, P ;
BEAUFAY, H ;
SELLINGER, OZ ;
RAHMANLI, Y ;
DEDUVE, C ;
WATTIAUX, R ;
JACQUES, P .
BIOCHEMICAL JOURNAL, 1964, 92 (01) :179-+
[5]  
BERGMEYER HU, 1983, METHOD ENZYMAT AN, V2, P130
[6]   RECENT PROGRESS ON REGULATION OF THE MITOCHONDRIAL PERMEABILITY TRANSITION PORE - A CYCLOSPORINE-SENSITIVE PORE IN THE INNER MITOCHONDRIAL-MEMBRANE [J].
BERNARDI, P ;
BROEKEMEIER, KM ;
PFEIFFER, DR .
JOURNAL OF BIOENERGETICS AND BIOMEMBRANES, 1994, 26 (05) :509-517
[7]  
Bobyleva V, 1997, BIOCHEM MOL BIOL INT, V41, P469
[8]   Mitochondrial cytochrome c release in apoptosis occurs upstream of DEVD-specific caspase activation and independently of mitochondrial transmembrane depolarization [J].
Bossy-Wetzel, E ;
Newmeyer, DD ;
Green, DR .
EMBO JOURNAL, 1998, 17 (01) :37-49
[9]   Neural apoptosis [J].
Bredesen, DE .
ANNALS OF NEUROLOGY, 1995, 38 (06) :839-851
[10]   Quantitative analysis of biological membrane lipids at the low picomole level by nano-electrospray ionization tandem mass spectrometry [J].
Brugger, B ;
Erben, G ;
Sandhoff, R ;
Wieland, FT ;
Lehmann, WD .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (06) :2339-2344