Heme oxygenase-1 and carbon monoxide regulate intestinal homeostasis and mucosal immune responses to the enteric microbiota

Gut Microbes. 2014 Mar-Apr;5(2):220-4. doi: 10.4161/gmic.27290. Epub 2013 Dec 20.

Abstract

Heme oxygenase-1 (HO-1) and its enzymatic by-product carbon monoxide (CO) have emerged as important regulators of acute and chronic inflammation. Mechanisms underlying their anti-inflammatory effects are only partially understood. In this addendum, we summarize current understanding of the role of the HO-1/CO pathway in regulation of intestinal inflammation with a focus on innate immune function. In particular, we highlight our recent findings that HO-1 and CO ameliorate intestinal inflammation through promotion of bacterial clearance. Our work and that of many others support further investigation of this global homeostatic pathway in the human inflammatory bowel diseases (IBDs).

Keywords: Crohn disease; carbon monoxide; heme oxygenase; macrophage; ulcerative colitis.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Colitis, Ulcerative / enzymology
  • Colitis, Ulcerative / immunology
  • Crohn Disease / enzymology
  • Crohn Disease / immunology
  • Heme Oxygenase-1 / metabolism*
  • Humans
  • Immunity, Mucosal / immunology
  • Inflammatory Bowel Diseases / immunology
  • Inflammatory Bowel Diseases / microbiology
  • Intestines / immunology
  • Intestines / microbiology*

Substances

  • Heme Oxygenase-1