IL-21 induces the apoptosis of resting and activated primary B cells |
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Authors: | Mehta Devangi S Wurster Andrea L Whitters Matthew J Young Deborah A Collins Mary Grusby Michael J |
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Affiliation: | Department of Immunology and Infectious Diseases, Harvard School of Public Health, and Genetics Institute, Wyeth Research, Cambridge, MA 02140, USA. |
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Abstract: | Cytokines play an important role in regulating the development and homeostasis of B cells by controlling their viability. In this study, we show that the recently described T cell-derived cytokine IL-21 induces the apoptosis of resting primary murine B cells. In addition, the activation of primary B cells with IL-4, LPS, or anti-CD40 Ab does not prevent IL-21-mediated apoptosis. The induction of apoptosis by IL-21 correlates with a down-regulation in the expression of Bcl-2 and Bcl-x(L), two antiapoptotic members of the Bcl-2 family. Furthermore, the reconstitution of Bcl-x(L) or Bcl-2 expression protects primary B cells from IL-21-induced apoptosis. In addition, a short-term preactivation of B cells with anti-CD40 Ab confers protection from IL-21-mediated apoptosis through the up-regulation of Bcl-x(L). These studies reveal a novel pathway that mediates B cell apoptosis via the IL-21R and suggest that IL-21 may play a role in regulating B cell homeostasis. |
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