Role of RAGE in lipopolysaccharide-induced cytoskeletal changes in mouse pulmonary microvascular endothelial cells.
- Author:
Xiao-Yan ZHOU
1
;
Wei-Jin ZHANG
;
Qiao-Bing HUANG
;
Xiao-Hua GUO
Author Information
- Publication Type:Journal Article
- MeSH: Actins; metabolism; Animals; Cells, Cultured; Cytoskeleton; metabolism; Endothelial Cells; cytology; Lipopolysaccharides; Lung; cytology; Mice; Mice, Knockout; Microvessels; cytology; Phenotype; Receptor for Advanced Glycation End Products; Receptors, Immunologic; genetics; metabolism
- From: Journal of Southern Medical University 2015;35(1):6-11
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo investigate lipopolysaccharide (LPS)-induced changes of cytoskeletal filamentous actin in primary isolated pulmonary microvascular endothelial cells (PMVECs) from wild-type and RAGE knock-out mouse.
METHODSThe lungs of wild-type and RAGE knock-out mice were digested with collagenase type I to obtain endothelial cells purified by anti-CD31-coupled magnetic beads. The PMVEC identified by factor VIII labeling were stimulated with LPS at different concentrations and the changes of filamentous actin were observed by confocal microscopy.
RESULTSThe cultured primary cells showed typical endothelial cell phenotype as examined with factor VIII labeling. LPS stimulation caused rearrangement of the cytoskeletal filament F-actin in wild-type mouse PMVECs with stress fiber formation, but such changes were not obvious in RAGE knock-out mouse PMVECs.
CONCLUSIONMouse PMVECs of a high purity can be obtained by immune magnetic beads. RAGE is involved in LPS-induced destruction of mouse PMVEC cytoskeletons.