Impaired Negative Selection of T Cells in Hodgkin's Disease Antigen CD30–Deficient Mice

نویسندگان

  • Ryuichi Amakawa
  • Anne Hakem
  • Thomas M Kundig
  • Toshifumi Matsuyama
  • John J.L Simard
  • Emma Timms
  • Andrew Wakeham
  • Hans-Willi Mittruecker
  • Henrik Griesser
  • Hiroaki Takimoto
  • Rudolf Schmits
  • Arda Shahinian
  • Pamela S Ohashi
  • Josef M Penninger
  • Tak W Mak
چکیده

CD30 is found on Reed-Sternberg cells of Hodgkin's disease and on a variety of non-Hodgkin's lymphoma cells and is up-regulated on cells after Epstein-Barr virus, human T cell leukemia virus, and HIV infections. We report here that the thymus in CD30-deficient mice contains elevated numbers of thymocytes. Activation-induced death of thymocytes after CD3 cross-linking is impaired both in vitro and in vivo. Breeding the CD30 mutation separately into alpha beta TCR-or gamma delta TCR-transgenic mice revealed a gross defect in negative but not positive selection. Thus, like TNF-receptors and Fas/Apo-1, the CD30 receptor is involved in cell death signaling. It is also an important coreceptor that participates in thymic deletion.

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عنوان ژورنال:
  • Cell

دوره 84  شماره 

صفحات  -

تاریخ انتشار 1996