[Role of RAGE in lipopolysaccharide-induced cytoskeletal changes in mouse pulmonary microvascular endothelial cells]

Nan Fang Yi Ke Da Xue Xue Bao. 2015 Jan;35(1):6-11.
[Article in Chinese]

Abstract

Objective: To 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.

Methods: The 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.

Results: The 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.

Conclusion: Mouse PMVECs of a high purity can be obtained by immune magnetic beads. RAGE is involved in LPS-induced destruction of mouse PMVEC cytoskeletons.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 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
  • Receptors, Immunologic / metabolism*

Substances

  • Actins
  • Lipopolysaccharides
  • Receptor for Advanced Glycation End Products
  • Receptors, Immunologic