Skip to main content

Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

  • Article
  • Published:

Heme oxygenase: A novel target for the modulation of inflammatory response

Abstract

Chronic inflammatory diseases place a heavy social and economic burden on the resources of many nations, but the number of safe and effective treatments is limited. To date, the major research effort has concentrated on those mediators responsible for the initiation and maintenance of the pathological process. In contrast, little attention has been focused on endogenous factors responsible for the resolution of the inflammation. Heme oxygenase ((HO); EC 1.14.99.3) is the rate–limiting enzyme in the catabolism of heme to biliverdin (which is converted to bilirubin by biliverdin reductase), free iron and carbon monoxide (CO). Two isoforms of HO have been characterized, the constitutive isoform, HO–2, which is the major isoform present under physiological conditions, and the stress–induced isoform, HO–1, which has also been classified as heat–shock protein 32K (ref. 1). Increases in HO activity have been implicated in tissue protection against oxidative stress2. In this communication, we describe the effects of modulating HO during an acute complement–dependent inflammatory response. Elevation of this enzyme resulted in a striking suppression, whereas inhibition of the enzyme led to a potentiation of the inflammatory response. Such novel enzyme modulation has application on the one hand to the treatment of inflammatory diseases and on the other hand to immunosuppressed states in which the impaired ability to mount an adequate inflammatory response may result in death from opportunistic infections.

This is a preview of subscription content, access via your institution

Access options

Buy this article

Prices may be subject to local taxes which are calculated during checkout

Similar content being viewed by others

References

  1. Maines, M.D. Heme oxygenase: Function, multiplicity, regulatory mechanisms, and clinical application. FASEB J. 2, 2557–2568 (1988).

    Article  CAS  Google Scholar 

  2. Nath, K.A. et al. Induction of heme oxygenase is a rapid, protective response in rhabdomyolysis in the rat. J. Clin. Invest. 90, 267–270 (1992).

    Article  CAS  Google Scholar 

  3. Capasso, F., Dunn, C.J., Yamamoto, S., Willoughby, D.A. & Giroud, R.A. Further studies on carrageenan-induced pleurisy in rats. J. Pathol. 116, 117–124 (1975).

    Article  CAS  Google Scholar 

  4. Cantoni, L., Rossi, C., Rizzardini, M., Gadina, M. & Ghezzi, P. Interleukin-1 and tumor necrosis factor induce hepatic haem oxygenase. Biochem. J. 279, 891–894 (1991).

    Article  CAS  Google Scholar 

  5. Keyse, S.M. & Tyrrell, R.M. Heme oxygenase is the major 32-kDa stress protein induced in the human skin fibroblasts by UV radiation, hydrogen peroxide and sodium arsenite. Proc. Natl. Acad. Sci. USA 86, 99–103 (1991).

    Article  Google Scholar 

  6. Polla, B.S., Stubbe, H., Kantengwa, S., Maridonneau-Parini, I. & Jacquier-Sarlin, M.R. Differential induction of stress proteins and functional effects of heat shock in human phagocytes. Inflammation 19, 363–371 (1995).

    Article  CAS  Google Scholar 

  7. Stacker, R., Yamamoto, Y. & McDonagh, A.F. Bilirubin is an antioxidant of possible physiological importance. Science 235, 1043–1046 (1987).

    Article  Google Scholar 

  8. Nakagami, T., Toyomura, K., Kinoshita, T. & Morisawa, S.A. A beneficial role of bile pigments as an endogenous tissue protector: Anti-complement effects of biliverdin and conjugated bilirubin. Biochim. Biophys. Acta. 1158, 189–193 (1993).

    Article  CAS  Google Scholar 

  9. Marks, G.S., Brien, J.F., Nakatsu, K. & McLaughlin, B.E. Does carbon monoxide have a physiological function? Trends Pharmacol. Sci. 12, 185–188 (1991).

    Article  CAS  Google Scholar 

  10. Morita, T., Perrella, M.A., Lee, M. & Kourembanas, S. Smooth muscle Cell-derived carbon-monoxide is a regulator of vascular cGMP. Proc. Natl. Acad. Sci. USA 92, 1475–1479 (1995).

    Article  CAS  Google Scholar 

  11. White, K.A. & Marietta, M.A. Nitric oxide synthase is a cytochrome P450 type hemoprotein. Biochemistry 31, 6627–6631 (1992).

    Article  CAS  Google Scholar 

  12. Martasek, P., Schwartzman, M.L. & Goodman, A.I. Hemin and L-arginine regulation of blood pressure in spontaneous hypersensitive rats. J. Am. Soc. Nephrol. 2, 1078–1084 (1993).

    Google Scholar 

  13. Tomlinson, A. et al. Cyclo-oxygenase and nitric oxide synthase isoforms in rat carrageenin-induced pleurisy. Br. J. Pharmac. 113, 693–698 (1994).

    Article  CAS  Google Scholar 

  14. Vane, J.R. et al. Inducible isoforms of cyclo-oxygenase and nitric oxide synthase in inflammation. Proc. Natl. Acad. Sci. USA 91, 2046–2050 (1994).

    Article  CAS  Google Scholar 

  15. Willis, D., Tomlinson, A., Frederick, R., Paul-Clark, M.J. & Willoughby, D.A. Modulation of heme oxygenase activity in rat brain and spleen by inhibitors and donors of nitric oxide. Biochem. Biophys. Res. Comtn. 214, 1152–1156 (1995).

    Article  CAS  Google Scholar 

  16. Levere, R.D. et al. Elevated levels of heme oxygenase-1 activity and mRNA in peripheral blood adherent cells of acquired immunodeficiency syndrome patients. Am. J. Hematol. 43, 19–23 (1993).

    Article  CAS  Google Scholar 

  17. Sierra, E.S. & Nutter, L.M.A. A microassay for heme oxygenase activity using thin-layer chromatography. Anal. Biochem. 200, 27–30 (1992).

    CAS  Google Scholar 

  18. Bradford, M.M. A rapid and sensitive method for the quantisation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal. Biochem. 72, 248–254 (1976).

    Article  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Willis, D., Moore, A., Frederick, R. et al. Heme oxygenase: A novel target for the modulation of inflammatory response. Nat Med 2, 87–90 (1996). https://doi.org/10.1038/nm0196-87

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1038/nm0196-87

This article is cited by

Search

Quick links

Nature Briefing

Sign up for the Nature Briefing newsletter — what matters in science, free to your inbox daily.

Get the most important science stories of the day, free in your inbox. Sign up for Nature Briefing