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CD40 激活诱导 bcl-x 可挽救小鼠 B 细胞中 sIg 诱导的细胞凋亡。

Induction of bcl-x by CD40 engagement rescues sIg-induced apoptosis in murine B cells.

作者信息

Wang Z, Karras J G, Howard R G, Rothstein T L

机构信息

Department of Medicine, Boston University Medical Center, MA 02118, USA.

出版信息

J Immunol. 1995 Oct 15;155(8):3722-5.

PMID:7561075
Abstract

CD40L, a membrane protein of activated T cells, interacts with the B cell receptor CD40. This interaction has been implicated in the rescue of germinal center B cells from apoptosis and in the rescue of WEHI-231 B lymphoma cells from sIg-induced apoptosis. In this report, we have demonstrated that the signal mediated by CD40L acts upon bcl-x, a bcl-2 homologue. bcl-x expression is strongly enhanced by CD40 receptor engagement, while there is little or no induction by sIg cross-linking. The expression of bax and bcl-2 is not significantly affected by either CD40L or sIg cross-linking. Antisense but not sense phosphorothioate oligonucleotide for bcl-x can partially block this CD40-mediated apoptotic rescue. This result suggests that the up-regulation of bcl-x by CD40L plays an important role in CD40-mediated apoptotic rescue in murine B cells.

摘要

CD40L是活化T细胞的一种膜蛋白,它与B细胞受体CD40相互作用。这种相互作用与从凋亡中拯救生发中心B细胞以及从sIg诱导的凋亡中拯救WEHI-231 B淋巴瘤细胞有关。在本报告中,我们已经证明由CD40L介导的信号作用于bcl-x,一种bcl-2同源物。通过CD40受体结合,bcl-x的表达被强烈增强,而通过sIg交联几乎没有诱导作用。bax和bcl-2的表达不受CD40L或sIg交联的显著影响。针对bcl-x的反义而非有义硫代磷酸酯寡核苷酸可以部分阻断这种CD40介导的凋亡拯救。该结果表明,CD40L对bcl-x的上调在小鼠B细胞的CD40介导的凋亡拯救中起重要作用。

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