Neutrophil heat shock protein expression and activation correlate with increased apoptosis following transmigration through the endothelial barrier

Citation
Sn. Hennigan et al., Neutrophil heat shock protein expression and activation correlate with increased apoptosis following transmigration through the endothelial barrier, SHOCK, 12(1), 1999, pp. 32-38
Citations number
31
Categorie Soggetti
Cardiovascular & Hematology Research
Journal title
SHOCK
ISSN journal
10732322 → ACNP
Volume
12
Issue
1
Year of publication
1999
Pages
32 - 38
Database
ISI
SICI code
1073-2322(199907)12:1<32:NHSPEA>2.0.ZU;2-G
Abstract
Polymorphonuclear leukocytes (PMN) undergo endothelial transmigration upon activation or in response to a chemoattractant Such cells are stressed and have an increased capacity to incite tissue injury, Little is known about t he effect of transmigration on PMN stress gene responses, PMN activation, a nd ultimately programmed cell death (apoptosis). Human endothelial cells (E CV-304) were plated onto transwell membranes to form an endothelial monolay er and PMN transendothelial migration through this endothelial barrier was examined. Chemotaxis was induced by formyl-methionyl-leucyl-phenylalanine ( fMLP). Flow cytometry was used to determine PMN receptor expression (CD11b, CD14, CD16, CD18, CD54), phagocytosis, and apoptosis, Heat shock protein ( Hsp) expression was evaluated by Western blotting. fMLP-induced PMN transen dothelial migration resulted in increased adhesion receptor expression and phagocytosis. Migrated PMN also had an increased rate of apoptosis as evalu ated by uptake of propidium iodide and decreased Fc gamma R III (CD16) expr ession. Increased PMN apoptosis coincided with induction of Hsp72 following transmigration. Thus, naive PMN that migrate through endothelium in respon se to a chemoattractant undergo activation as represented by increased phag ocytosis and expression of adhesion receptors.