Estrogen deficiency induces bone loss by increasing T cell proliferation and lifespan through IFN-gamma-induced class II transactivator.

نویسندگان

  • Simone Cenci
  • Gianluca Toraldo
  • M Neale Weitzmann
  • Cristiana Roggia
  • Yuhao Gao
  • Wei Ping Qian
  • Oscar Sierra
  • Roberto Pacifici
چکیده

Expansion of the pool of tumor necrosis factor (TNF)-alpha-producing T cells is instrumental for the bone loss induced by estrogen deficiency, but the responsible mechanism is unknown. Here we show that ovariectomy up-regulates IFN-gamma-induced class II transactivator, a multitarget immune modulator, resulting in increased antigen presentation by macrophages, enhanced T cell activation, and prolonged lifespan of active T cells. Up-regulation of class II transactivator derives from increased production of IFN-gamma by T helper 1 cells, resulting from enhanced secretion of IL-12 and IL-18 by macrophages. The resulting T cell expansion and bone loss are prevented in vivo by both blockade of antigen presenting cell-induced T cell activation, and silencing of IFN-gamma receptor signaling. Thus, increased IFN-gamma-induced class II transactivator expression and the resulting enhanced T cell proliferation and lifespan are critical to the bone wasting effect of estrogen deficiency.

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عنوان ژورنال:
  • Proceedings of the National Academy of Sciences of the United States of America

دوره 100 18  شماره 

صفحات  -

تاریخ انتشار 2003