Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
3
pubmed:dateCreated
1999-3-4
pubmed:abstractText
The average polymorphonuclear neutrophil (PMN) lives only a day and then dies by apoptosis. We previously found that the calcium-dependent protease calpain is required for apoptosis in several mouse models of cell death. Here we identify calpain, and its endogenous inhibitor calpastatin, as regulators of human neutrophil apoptosis. Cell death triggered by the translation inhibitor cycloheximide is calpain-dependent, as evidenced using either a calpain active site inhibitor (N-acetyl-leucyl-leucyl-norleucinal) or agents that target calpain's calcium binding sites (PD150606, PD151746). No significant effect on cycloheximide-triggered apoptosis was found by using inhibitors of the proteasome or of other papain-like cysteine proteases, providing further evidence that the active site calpain inhibitor prevents apoptosis via its action on calpain. In addition, we find that potentiation of calpain activity by depleting its endogenous inhibitor, calpastatin, is sufficient to cause apoptosis of neutrophils. Nevertheless, apoptosis signalled via the Fas antigen proceeds regardless of the presence of calpain inhibitor. These experiments support a growing body of work, indicating an upstream regulatory role for calpain in many, but not all, forms of apoptotic cell death. They also identify calpastatin as a participant in apoptotic cell death and suggest that for at least one cell type, a decrease in calpastatin is a sufficient stimulus to initiate calpain-dependent apoptosis.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Mar
pubmed:issn
0021-9541
pubmed:author
pubmed:issnType
Print
pubmed:volume
178
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
311-9
pubmed:dateRevised
2007-11-14
pubmed:meshHeading
pubmed-meshheading:9989777-Acrylates, pubmed-meshheading:9989777-Adult, pubmed-meshheading:9989777-Animals, pubmed-meshheading:9989777-Apoptosis, pubmed-meshheading:9989777-Calcium-Binding Proteins, pubmed-meshheading:9989777-Calpain, pubmed-meshheading:9989777-Cell Survival, pubmed-meshheading:9989777-Cells, Cultured, pubmed-meshheading:9989777-Cycloheximide, pubmed-meshheading:9989777-Cysteine Proteinase Inhibitors, pubmed-meshheading:9989777-Humans, pubmed-meshheading:9989777-Kinetics, pubmed-meshheading:9989777-Mice, pubmed-meshheading:9989777-Neutrophils, pubmed-meshheading:9989777-Oligodeoxyribonucleotides, Antisense, pubmed-meshheading:9989777-Protein Biosynthesis, pubmed-meshheading:9989777-RNA, Messenger, pubmed-meshheading:9989777-Thionucleotides, pubmed-meshheading:9989777-Transcription, Genetic
pubmed:year
1999
pubmed:articleTitle
Calpain and calpastatin regulate neutrophil apoptosis.
pubmed:affiliation
Department of Immunology, School of Medicine, University of Colorado Health Sciences Center, Denver 80262, USA. Peg.Squier@uchsc.edu
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S., Research Support, Non-U.S. Gov't