B cell apoptosis triggered by antigen receptor ligation proceeds via a novel caspase-dependent pathway

W Chen, HG Wang, SM Srinivasula… - The Journal of …, 1999 - journals.aai.org
W Chen, HG Wang, SM Srinivasula, ES Alnemri, NR Cooper
The Journal of Immunology, 1999journals.aai.org
In contrast to positive signaling leading to proliferation, the mechanisms involved in negative
signaling culminating in apoptosis after B cell Ag receptor (BCR) ligation have received little
study. We find that apoptosis induced by BCR cross-linking on EBV-negative mature and
immature human B cell lines involves the following sequential, required events: a
cyclosporin A-inhibitable, likely calcineurin-mediated step; and activation of caspase-2,-3,
and-9. Caspase-2 is activated early and plays a major role in the apoptotic pathway, while …
Abstract
In contrast to positive signaling leading to proliferation, the mechanisms involved in negative signaling culminating in apoptosis after B cell Ag receptor (BCR) ligation have received little study. We find that apoptosis induced by BCR cross-linking on EBV-negative mature and immature human B cell lines involves the following sequential, required events: a cyclosporin A-inhibitable, likely calcineurin-mediated step; and activation of caspase-2,-3, and-9. Caspase-2 is activated early and plays a major role in the apoptotic pathway, while caspase-9 is activated later in the apoptotic pathway and most likely functions to amplify the apoptotic signal. Caspase-8 and-1, which are activated by ligation of the CD95 and TNF-R1 death receptors, are not involved. Apoptosis induced by BCR ligation thus proceeds via a previously unreported intracellular signaling pathway.
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