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PMID: 10438567 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Annexin V staining due to loss of membrane asymmetry can be reversible and precede commitment to apoptotic death.

Experimental cell research ·Vol. 251 ·No. 1 ·1999-08-25 ·Pages 16-21

Hammill AK, Uhr JW, Scheuermann RH

Abstract

Signal-induced apoptosis is a normal phenomenon in which cells respond to changes in their environment through a cascade of intracellular biochemical changes culminating in cell death. However, it is not clear at what point in this process the cell becomes committed to die. An early biochemical change characteristic of cells undergoing apoptosis is the loss of plasma membrane asymmetry, such that high levels of phosphatidylserine become exposed on the outside cell surface. These cells can be recognized by staining with Annexin V, which binds to phosphatidylserine with high affinity. To investigate the mechanisms controlling signal-induced apoptosis we have examined the response of a B cell lymphoma to crosslinking of the membrane immunoglobulin (mIg) receptor. We have found that many of the cells that stain positive for Annexin V are viable and can resume growth and reestablish phospholipid asymmetry once the signal is removed. These results indicate that Annexin V staining, and thus loss of membrane asymmetry, precedes commitment to apoptotic death in this system.

MeSH Terms
Animals Annexin A5/metabolism Antibodies Apoptosis/drug effects B-Lymphocytes/cytology,immunology,metabolism Cell Count Cell Membrane/metabolism Cell Survival Lymphocyte Activation Mice Phosphatidylserines/metabolism Propidium Receptor Aggregation Receptors, Antigen, B-Cell/metabolism Signal Transduction Trypan Blue Tumor Cells, Cultured
Chemicals
Annexin A5 Antibodies Phosphatidylserines Receptors, Antigen, B-Cell Propidium Trypan Blue
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Hammill A K
Laboratory of Molecular Pathology, Department of Microbiology, University of Texas Southwestern Medical Center, 5323 Harry Hines Boulevard, Dallas, Texas 75235, USA.
Uhr J W
Scheuermann R H
Article Info
Journal
Experimental cell research
Abbr.
Exp Cell Res
ISSN
0014-4827
Published
1999-08-25
Pages
16-21
Language
English
Region
United States
NLM ID
0373226
Subset
IM
Grants
NCI NIH HHS · CA78793 · United States
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