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Publication : Alpha (v) integrins license regulatory T cells to apoptotic cells and self-associated antigens.

First Author  Païdassi H Year  2010
Journal  Ann N Y Acad Sci Volume  1209
Pages  68-76 PubMed ID  20958318
Mgi Jnum  J:175327 Mgi Id  MGI:5285146
Doi  10.1111/j.1749-6632.2010.05783.x Citation  Paidassi H, et al. (2010) Alpha (v) integrins license regulatory T cells to apoptotic cells and self-associated antigens. Ann N Y Acad Sci 1209:68-76
abstractText  Defects in apoptotic cell clearance are thought to contribute to autoimmunity by failure to induce tolerance, coupled with accumulation of immunogenic material. However, little is known about the contribution of apoptosis to immune responses at mucosal sites, where regulatory T cells (T(reg) cells) and other immune cells play an essential active role in maintaining tolerance to self-associated antigens. In recent studies, we have found that alpha(v) integrins have an important role in apoptotic cell phagocytosis and induction of T(reg) cells in the intestine, and deletion of alpha(v) from myeloid cells causes colitis associated with failed apoptotic cell removal and loss of T(reg) cells. Our data show that activation of transforming growth factor (TGF)-beta by alpha(v) beta(8) on dendritic cells (DCs) is essential for generating T(reg) cells and inducing mucosal tolerance. These results provide a mechanism by which tolerance to apoptotic cell-derived and -associated antigens is maintained by DC 'licensing' at sites of high TGF-beta expression.
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