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白细胞介素-21诱导静止和活化的原代B细胞凋亡。

IL-21 induces the apoptosis of resting and activated primary B cells.

作者信息

Mehta Devangi S, Wurster Andrea L, Whitters Matthew J, Young Deborah A, Collins Mary, Grusby Michael J

机构信息

Department of Immunology and Infectious Diseases, Harvard School of Public Health, and Genetics Institute, Wyeth Research, Cambridge, MA 02140, USA.

出版信息

J Immunol. 2003 Apr 15;170(8):4111-8. doi: 10.4049/jimmunol.170.8.4111.

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.

摘要

细胞因子通过控制B细胞的活力,在调节B细胞的发育和内环境稳定中发挥重要作用。在本研究中,我们发现最近描述的T细胞衍生细胞因子IL-21可诱导静止的原代小鼠B细胞凋亡。此外,用IL-4、LPS或抗CD40抗体激活原代B细胞并不能阻止IL-21介导的凋亡。IL-21诱导的凋亡与Bcl-2家族的两个抗凋亡成员Bcl-2和Bcl-x(L)表达下调相关。此外,Bcl-x(L)或Bcl-2表达的重建可保护原代B细胞免受IL-21诱导的凋亡。此外,用抗CD40抗体对B细胞进行短期预激活可通过上调Bcl-x(L)赋予其对IL-21介导凋亡的保护作用。这些研究揭示了一条通过IL-21R介导B细胞凋亡的新途径,并表明IL-21可能在调节B细胞内环境稳定中发挥作用。

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