MyD88 and Src are differentially regulated in Kupffer cells of males and proestrus females following hypoxia

Mol Med. 2006 Apr-Jun;12(4-6):65-73. doi: 10.2119/2006-00030.Zheng.

Abstract

Hypoxia produces sex dimorphic immune responses in males and proestrus females. Because Kupffer cells are the major source of proinflammatory cytokines, studies were conducted to discern IL-6 production in mouse Kupffer cells following hypoxia. Hypoxia enhances TLR4 expression in Kupffer cells irrespective of sex. However, MyD88 and Src expression in Kupffer cells decreased significantly after hypoxia in proestrus females, whereas Src protein expression and phosphorylation increased in males in concurrence with differences in IL-6 production. 17beta-estradiol administration elevated MyD88 and Src expression in males to levels in normoxic proestrus females. Administration of Src inhibitor in hypoxic males prevented increased IL-6 production. Thus, differential regulation of MyD88 and Src in males and females plays an important role in sex-specific immune response following hypoxia.

Publication types

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

MeSH terms

  • Animals
  • Cell Culture Techniques
  • Cells, Cultured
  • Estradiol / pharmacology
  • Female
  • Hypoxia / immunology*
  • Interleukin-6 / analysis
  • Interleukin-6 / biosynthesis
  • Kupffer Cells / drug effects
  • Kupffer Cells / immunology*
  • Male
  • Mice
  • Mice, Inbred C3H
  • Myeloid Differentiation Factor 88 / genetics
  • Myeloid Differentiation Factor 88 / metabolism*
  • Phosphorylation
  • Proestrus / immunology*
  • Pyrazoles / pharmacology
  • Pyrimidines / pharmacology
  • Sex Characteristics*
  • Toll-Like Receptor 4 / immunology
  • Toll-Like Receptor 4 / metabolism
  • src-Family Kinases / antagonists & inhibitors
  • src-Family Kinases / metabolism*

Substances

  • 4-amino-5-(4-methylphenyl)-7-(tert-butyl)pyrazolo(3,4-d)pyrimidine
  • Interleukin-6
  • Myd88 protein, mouse
  • Myeloid Differentiation Factor 88
  • Pyrazoles
  • Pyrimidines
  • Toll-Like Receptor 4
  • Estradiol
  • src-Family Kinases