Herpesvirus entry mediator regulates hypoxia-inducible factor-1α and erythropoiesis in mice

J Clin Invest. 2011 Dec;121(12):4810-9. doi: 10.1172/JCI57332. Epub 2011 Nov 14.

Abstract

Erythropoiesis, the production of red blood cells, must be tightly controlled to ensure adequate oxygen delivery to tissues without causing thrombosis or stroke. Control of physiologic and pathologic erythropoiesis is dependent predominantly on erythropoietin (EPO), the expression of which is regulated by hypoxia-inducible factor (HIF) activity in response to low oxygen tension. Accumulating evidence indicates that oxygen-independent mediators, including inflammatory stimuli, cytokines, and growth factors, also upregulate HIF activity, but it is unclear whether these signals also result in EPO production and erythropoiesis in vivo. Here, we found that signaling through herpesvirus entry mediator (HVEM), a molecule of the TNF receptor superfamily, promoted HIF-1α activity in the kidney and subsequently facilitated renal Epo production and erythropoiesis in vivo under normoxic conditions. This Epo upregulation was mediated by increased production of NO by renal macrophages. Hvem-deficient mice displayed impaired Epo expression and aggravated anemia in response to erythropoietic stress. These data reveal that HVEM signaling functions to promote HIF-1α activity and Epo production, and thus to regulate erythropoiesis. Furthermore, our findings suggest that this molecular mechanism could represent a therapeutic target for Epo-responsive diseases, including anemia.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Antibodies, Monoclonal / immunology
  • Antibodies, Monoclonal / pharmacology
  • Cell Hypoxia
  • Erythropoiesis / physiology*
  • Erythropoietin / biosynthesis*
  • Erythropoietin / genetics
  • Female
  • Gene Expression Profiling
  • Hypoxia-Inducible Factor 1, alpha Subunit / biosynthesis*
  • Hypoxia-Inducible Factor 1, alpha Subunit / genetics
  • Kidney / metabolism*
  • Macrophages / metabolism
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Nitric Oxide / physiology
  • Oxygen / physiology
  • Radiation Chimera
  • Receptors, Tumor Necrosis Factor, Member 14 / agonists
  • Receptors, Tumor Necrosis Factor, Member 14 / deficiency
  • Receptors, Tumor Necrosis Factor, Member 14 / genetics
  • Receptors, Tumor Necrosis Factor, Member 14 / immunology
  • Receptors, Tumor Necrosis Factor, Member 14 / physiology*
  • Signal Transduction / physiology

Substances

  • Antibodies, Monoclonal
  • Hypoxia-Inducible Factor 1, alpha Subunit
  • Receptors, Tumor Necrosis Factor, Member 14
  • Tnfrsf14 protein, mouse
  • Erythropoietin
  • Nitric Oxide
  • Oxygen