Control of endothelial barrier function by regulating vascular endothelial-cadherin

Vestweber D, Broermann A, Schulte D

Forschungsartikel (Zeitschrift)

Zusammenfassung

Purpose of review Proper control of endothelial cell contacts is the basis for maintenance of the vascular barrier function. Loss of this function leads to leak of fluid and protein from the vasculature and extensive leaks cause shock and death. The endothelial barrier also controls the entry of leukocytes into tissue and it is believed that leukocytes target endothelial cell contacts to reach sites of inflammation. Recent findings Within the last 2 years several new molecular players and molecular interactions have been identified that either help in stabilizing the endothelial contacts or mediate their opening if triggered by the appropriate stimuli. Novel signaling mechanisms have been identified that regulate endothelial cell contacts. Whether, how and to what extent the complex of the endothelial specific adhesion molecule vascular endothelial-cadherin and its associated catenins is involved in these processes will be a major focus of this article. Summary Endothelial cell contacts are regulated by a complex interplay between various receptors and signaling mediators that control the plasticity of the cytoskeleton and the function of junctional adhesion molecules. Knowing and understanding the essential players of this network will allow development of agents that could prevent breakdown of the vascular permeability barrier in shock or that could block leukocyte extravasation and thereby antagonize inflammation.

Details zur Publikation

FachzeitschriftCurrent Opinion in Hematology
Jahrgang / Bandnr. / Volume17
Ausgabe / Heftnr. / Issue3
Seitenbereich230-236
StatusVeröffentlicht
Veröffentlichungsjahr2010 (31.05.2010)
Sprache, in der die Publikation verfasst istEnglisch
Stichwörterendothelial cell contacts leukocyte extravasation vascular endothelial-cadherin vascular permeability lung microvascular endothelia blood-vessel development phosphatase ve-ptp tyrosine phosphorylation cell-cell growth-factor paracellular pathway beta-catenin transcellular migration adherens junctions

Autor*innen der Universität Münster

Vestweber, Dietmar
Max-Planck-Institut für Molekulare Biomedizin