|
|
||||||||
The Journal of Immunology, Vol 154, Issue 2 599-609, Copyright © 1995 by American Association of Immunologists
ARTICLES |
Y Oshimi and S Miyazaki
Department of Physiology, Tokyo Women's Medical College, Japan.
More than 80% of cells of the human B cell line FMO, which expresses the Fas Ag, underwent apoptosis within 2 h after addition of an anti- Fas mAb. Rises in cytosolic Ca2+ concentration ([Ca2+]i) and their effects were investigated by imaging individual cells continuously and introducing Ca2+ chelators to the outside and/or inside of the cell. The typical Ca2+ response consisted of 1) an early [Ca2+]i rise (basal [Ca2+]i, 85 to 110 nM; peak, 140 to 200 nM; duration, 15 to 20 min), 2) sustained elevation of [Ca2+]i at 140 to 150 nM, 3) a second Ca2+ rise (200 to 500 nM, 15 to 30 min) between 1.5 and 2 h, and 4) a large [Ca2+]i rise (1.2 to 2.0 microM) between 2 and 4 h after addition of mAb. Responses 1, 3, and 4 were mainly caused by Ca2+ entry, and response 2 involved intracellular Ca2+ release from stores. Apoptosis could be induced by mAb even in Ca(2+)-deprived external medium. Chelating cytosolic Ca2+ revealed that the [Ca2+]i rise is a prerequisite for fragmentation of DNA and chromatin, and is also necessary for fragmentation of cells. The critical [Ca2+]i was 140 to 150 nM and a sustained [Ca2+]i rise was more effective. A [Ca2+]i rise itself (without mAb) was ineffective. About 20% of mAb-treated cells showed chromatin condensation at the periphery of the nucleus (possibly an earlier stage of nuclear change) and a bubble-like cell shape even when [Ca2+]i was held below 100 nM. Thus, Ca2+ is mobilized immediately after Fas stimulation and functions as a key factor causing advanced apoptotic changes. Response 4 was related to secondary necrosis.
This article has been cited by other articles:
![]() |
A. L. Wozniak, X. Wang, E. S. Stieren, S. G. Scarbrough, C. J. Elferink, and D. Boehning Requirement of biphasic calcium release from the endoplasmic reticulum for Fas-mediated apoptosis J. Cell Biol., December 4, 2006; 175(5): 709 - 714. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. Maruyama, G. Takemura, N. Tohse, T. Ohkusa, Y. Ikeda, K. Tsuchiya, S. Minatoguchi, M. Matsuzaki, T. Fujiwara, and H. Fujiwara Synchronous progression of calcium transient-dependent beating and sarcomere destruction in apoptotic adult cardiomyocytes Am J Physiol Heart Circ Physiol, April 1, 2006; 290(4): H1493 - H1502. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Gomez-Angelats and J. A. Cidlowski Invited Review: Cell Volume Control and Signal Transduction in Apoptosis Toxicol Pathol, August 1, 2002; 30(5): 541 - 551. [Abstract] [PDF] |
||||
![]() |
R. Maruyama, G. Takemura, T. Aoyama, K. Hayakawa, M. Koda, Y. Kawase, X. Qiu, Y. Ohno, S. Minatoguchi, K. Miyata, et al. Dynamic Process of Apoptosis in Adult Rat Cardiomyocytes Analyzed Using 48-Hour Videomicroscopy and Electron Microscopy : Beating and Rate are Associated with the Apoptotic Process Am. J. Pathol., August 1, 2001; 159(2): 683 - 691. [Abstract] [Full Text] |
||||
![]() |
I. Medana, Z. Li, A. Flugel, J. Tschopp, H. Wekerle, and H. Neumann Fas Ligand (CD95L) Protects Neurons Against Perforin- Mediated T Lymphocyte Cytotoxicity J. Immunol., July 15, 2001; 167(2): 674 - 681. [Abstract] [Full Text] [PDF] |
||||
![]() |
Y. Kawasaki, T. Saito, Y. Shirota-Someya, Y. Ikegami, H. Komano, M.-H. Lee, C. J. Froelich, N. Shinohara, and H. Takayama Cell Death-Associated Translocation of Plasma Membrane Components Induced by CTL J. Immunol., May 1, 2000; 164(9): 4641 - 4648. [Abstract] [Full Text] [PDF] |
||||
![]() |
B. S. Kristal and A. M. Brown Apoptogenic Ganglioside GD3 Directly Induces the Mitochondrial Permeability Transition J. Biol. Chem., August 13, 1999; 274(33): 23169 - 23175. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. N. Orlov, N. Thorin-Trescases, S. V. Kotelevtsev, J. Tremblay, and P. Hamet Inversion of the Intracellular Na+/K+ Ratio Blocks Apoptosis in Vascular Smooth Muscle at a Site Upstream of Caspase-3 J. Biol. Chem., June 4, 1999; 274(23): 16545 - 16552. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. V. Mikhalap, L. M. Shlapatska, A. G. Berdova, C.-L. Law, E. A. Clark, and S. P. Sidorenko CDw150 Associates with Src-Homology 2-Containing Inositol Phosphatase and Modulates CD95-Mediated Apoptosis J. Immunol., May 15, 1999; 162(10): 5719 - 5727. [Abstract] [Full Text] [PDF] |
||||
![]() |
P. Vito, L. Pellegrini, C. Guiet, and L. D'Adamio Cloning of AIP1, a Novel Protein That Associates with the Apoptosis-linked Gene ALG-2 in a Ca2+-dependent Reaction J. Biol. Chem., January 15, 1999; 274(3): 1533 - 1540. [Abstract] [Full Text] [PDF] |
||||
![]() |
B. Felzen, M. Shilkrut, H. Less, I. Sarapov, G. Maor, R. Coleman, R. B. Robinson, G. Berke, and O. Binah Fas (CD95/Apo-1)–Mediated Damage to Ventricular Myocytes Induced by Cytotoxic T Lymphocytes From Perforin-Deficient Mice : A Major Role for Inositol 1,4,5-Trisphosphate Circ. Res., March 9, 1998; 82(4): 438 - 450. [Abstract] [Full Text] [PDF] |
||||
![]() |
F. LANG, G. L. BUSCH, M. RITTER, H. VOLKL, S. WALDEGGER, E. GULBINS, and D. HAUSSINGER Functional Significance of Cell Volume Regulatory Mechanisms Physiol Rev, January 1, 1998; 78(1): 247 - 306. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. P. Sheehan, R. H. Swerdlow, S. W. Miller, R. E. Davis, J. K. Parks, W. D. Parker, and J. B. Tuttle Calcium Homeostasis and Reactive Oxygen Species Production in Cells Transformed by Mitochondria from Individuals with Sporadic Alzheimer's Disease J. Neurosci., June 15, 1997; 17(12): 4612 - 4622. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. B. Scoltock, C. D. Bortner, G. St. J. Bird, J. W. Putney Jr., and J. A. Cidlowski A Selective Requirement for Elevated Calcium in DNA Degradation, but Not Early Events in Anti-Fas-induced Apoptosis J. Biol. Chem., September 22, 2000; 275(39): 30586 - 30596. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |