Pericyte requirement for anti-leak action of angiopoietin-1 and vascular remodeling in sustained inflammation.

Journal Article (Journal Article)

Blood vessel leakiness is an early, transient event in acute inflammation but can also persist as vessels undergo remodeling in sustained inflammation. Angiopoietin/Tie2 signaling can reduce the leakiness through changes in endothelial cells. The role of pericytes in this action has been unknown. We used the selective PDGF-B-blocking oligonucleotide aptamer AX102 to determine whether disruption of pericyte-endothelial crosstalk alters vascular leakiness or remodeling in the airways of mice under four different conditions: i) baseline, ii) acute inflammation induced by bradykinin, iii) sustained inflammation after 7-day infection by the respiratory pathogen Mycoplasma pulmonis, or iv) leakage after bradykinin challenge in the presence of vascular stabilization by the angiopoietin-1 (Ang1) mimic COMP-Ang1 for 7 days. AX102 reduced pericyte coverage but did not alter the leakage of microspheres from tracheal blood vessels at baseline or after bradykinin; however, AX102 exaggerated leakage at 7 days after M. pulmonis infection and increased vascular remodeling and disease severity at 14 days. AX102 also abolished the antileakage effect of COMP-Ang1 at 7 days. Together, these findings show that pericyte contributions to endothelial stability have greater dependence on PDGF-B during the development of sustained inflammation, when pericyte dynamics accompany vascular remodeling, than under baseline conditions or in acute inflammation. The findings also show that the antileakage action of Ang1 requires PDGF-dependent actions of pericytes in maintaining endothelial stability.

Full Text

Duke Authors

Cited Authors

  • Fuxe, J; Tabruyn, S; Colton, K; Zaid, H; Adams, A; Baluk, P; Lashnits, E; Morisada, T; Le, T; O'Brien, S; Epstein, DM; Koh, GY; McDonald, DM

Published Date

  • June 2011

Published In

Volume / Issue

  • 178 / 6

Start / End Page

  • 2897 - 2909

PubMed ID

  • 21550017

Pubmed Central ID

  • PMC3124300

Electronic International Standard Serial Number (EISSN)

  • 1525-2191

Digital Object Identifier (DOI)

  • 10.1016/j.ajpath.2011.02.008

Language

  • eng

Conference Location

  • United States