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Publication : Clonal deletion and the fate of autoreactive thymocytes that survive negative selection.

First Author  Pobezinsky LA Year  2012
Journal  Nat Immunol Volume  13
Issue  6 Pages  569-78
PubMed ID  22544394 Mgi Jnum  J:186451
Mgi Id  MGI:5432326 Doi  10.1038/ni.2292
Citation  Pobezinsky LA, et al. (2012) Clonal deletion and the fate of autoreactive thymocytes that survive negative selection. Nat Immunol 13(6):569-78
abstractText  Clonal deletion of autoreactive thymocytes is important for self-tolerance, but the intrathymic signals that induce clonal deletion have not been clearly identified. We now report that clonal deletion during negative selection required CD28-mediated costimulation of autoreactive thymocytes at the CD4(+)CD8(lo) intermediate stage of differentiation. Autoreactive thymocytes were prevented from undergoing clonal deletion by either a lack of CD28 costimulation or transgenic overexpression of the antiapoptotic factors Bcl-2 or Mcl-1, with surviving thymocytes differentiating into anergic CD4(-)CD8(-) double-negative thymocytes positive for the T cell antigen receptor alphabeta subtype (TCRalphabeta) that 'preferentially' migrated to the intestine, where they re-expressed CD8alpha and were sequestered as CD8alphaalpha(+) intraepithelial lymphocytes (IELs). Our study identifies costimulation by CD28 as the intrathymic signal required for clonal deletion and identifies CD8alphaalpha(+) IELs as the developmental fate of autoreactive thymocytes that survive negative selection.
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