Soluble endostatin is a novel inhibitor of epithelial repair in idiopathic pulmonary fibrosis

A.G. Richter, S. McKeown, S. Rathinam, L. Harper, P. Rajesh, Danny McAuley, R. Heljasvaara, D.R. Thickett

Research output: Contribution to journalArticlepeer-review

52 Citations (Scopus)

Abstract

Background and aim: Aberrant angiogenesis and defective epithelial repair are key features of idiopathic pulmonary fibrosis (IPF). Endostatin is an antiangiogenic peptide with known effects on endothelial cells. This study aimed to establish the levels of endostatin in the bronchoalveolar lavage fluid (BALF) in IPF and to investigate its actions on distal lung epithelial cells (DLEC) and primary type II cells.
Original languageEnglish
Pages (from-to)156-161
Number of pages6
JournalThorax
Volume64
Issue number2
DOIs
Publication statusPublished - Feb 2009

ASJC Scopus subject areas

  • Pulmonary and Respiratory Medicine

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