Angiopoietin-2 sensitizes endothelial cells to TNF-α and has a crucial role in the induction of inflammation

U Fiedler, Y Reiss, M Scharpfenecker, V Grunow… - Nature medicine, 2006 - nature.com
U Fiedler, Y Reiss, M Scharpfenecker, V Grunow, S Koidl, G Thurston, NW Gale…
Nature medicine, 2006nature.com
Abstract The angiopoietins Ang-1 and Ang-2 have been identified as ligands of the receptor
tyrosine kinase Tie-2 (refs.,). Paracrine Ang-1–mediated activation of Tie-2 acts as a
regulator of vessel maturation and vascular quiescence,. In turn, the antagonistic ligand Ang-
2 acts by an autocrine mechanism,, and is stored in endothelial Weibel-Palade bodies from
where it can be rapidly released upon stimulation. The rapid release of Ang-2 implies
functions of the angiopoietin-Tie system beyond its established role during vascular …
Abstract
The angiopoietins Ang-1 and Ang-2 have been identified as ligands of the receptor tyrosine kinase Tie-2 (refs. ,). Paracrine Ang-1–mediated activation of Tie-2 acts as a regulator of vessel maturation and vascular quiescence,. In turn, the antagonistic ligand Ang-2 acts by an autocrine mechanism,, and is stored in endothelial Weibel-Palade bodies from where it can be rapidly released upon stimulation. The rapid release of Ang-2 implies functions of the angiopoietin-Tie system beyond its established role during vascular morphogenesis as a regulator of rapid vascular responses. Here we show that mice deficient in Ang-2 (encoded by the gene Angpt2) cannot elicit an inflammatory response in thioglycollate-induced or Staphylococcus aureus–induced peritonitis, or in the dorsal skinfold chamber model. Recombinant Ang-2 restores the inflammation defect in Angpt2−/− mice. Intravital microscopy showed normal TNF-α–induced leukocyte rolling in the vasculature of Angpt2−/−mice, but rolling cells did not firmly adhere to activated endothelium. Cellular experiments showed that Ang-2 promotes adhesion by sensitizing endothelial cells toward TNF-α and modulating TNF-α–induced expression of endothelial cell adhesion molecules. Together, these findings identify Ang-2 as an autocrine regulator of endothelial cell inflammatory responses. Ang-2 thereby acts as a switch of vascular responsiveness exerting a permissive role for the activities of proinflammatory cytokines.
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