Cytosolic and endoplasmic reticulum Ca2+ concentrations determine the extent and the morphological type of apoptosis, respectively

被引:18
作者
Cerella, C
D'Alessio, M
De Nicola, M
Magrini, A
Bergamaschi, A
Ghibelli, L
机构
[1] Univ Roma Tor Vergata, Dipartimento Biol, I-00133 Rome, Italy
[2] Univ Roma Tor Vergata, Cattedra Med Lavoro, I-00133 Rome, Italy
来源
APOPTOSIS: FROM SIGNALING PATHWAYS TO THERAPEUTIC TOOLS | 2003年 / 1010卷
关键词
apoptosis; calcium; endoplasmic reticulum; apoptotic morphology;
D O I
10.1196/annals.1299.011
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
During apoptosis, an increase in cytosolic Ca2+ concentration ([Ca2+](c)) accompanies the depletion of endoplasmic reticulum (ER). The actual roles of each of the two events in apoptosis are difficult to understand. In this work, we have modulated the basal [Ca2+](c) and the thapsigargin (THG)-dependent reticular flux (i.e., by chelating extracellular Ca2+ or by modulating intracellular Ca2+ by 3-aminobenzamide [3-ABA]). We have found that these treatments alter these Ca2+ parameters in a differential way and, accordingly, affect apoptosis differentially. We have found that the increase in [Ca2+](c) is related to the extent of apoptosis, whereas the ER depletion affects the apoptotic nuclear morphology by shifting it towards the cleavage mode.
引用
收藏
页码:74 / 77
页数:4
相关论文
共 4 条
[1]   Magnetic fields increase cell survival by inhibiting apoptosis via modulation of Ca2+ influx [J].
Fanelli, C ;
Coppola, S ;
Barone, R ;
Colussi, C ;
Gualandi, G ;
Volpe, P ;
Ghibelli, L .
FASEB JOURNAL, 1999, 13 (01) :95-102
[2]  
GRYNKIEWICZ G, 1985, J BIOL CHEM, V260, P3440
[3]   EVIDENCE THAT BCL-2 REPRESSES APOPTOSIS BY REGULATING ENDOPLASMIC RETICULUM-ASSOCIATED CA2+ FLUXES [J].
LAM, M ;
DUBYAK, G ;
CHEN, L ;
NUNEZ, G ;
MIESFELD, RL ;
DISTELHORST, CW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (14) :6569-6573
[4]   POSSIBLE INVOLVEMENT OF POLY(ADP-RIBOSYL) POLYMERASE IN TRIGGERING STRESS-INDUCED APOPTOSIS [J].
NOSSERI, C ;
COPPOLA, S ;
GHIBELLI, L .
EXPERIMENTAL CELL RESEARCH, 1994, 212 (02) :367-373