Rel-dependent induction of A1 transcription is required to protect B cells from antigen receptor ligation-induced apoptosis
Details
Publication Year 1999-02-15,Volume 13,Issue #4,Page 400-411
Journal Title
GENES & DEVELOPMENT
Publication Type
Journal Article
Abstract
In response to different extracellular signals, Rel/NF-kappa B transcription factors are critical regulators of apoptosis in a variety of cell types. Here we show that in normal B and T cells, expression of the Bcl-2 prosurvival homolog, Al, is rapidly induced in a Rel-dependent manner by mitogens. In B-cell lines derived from c-rel(-/-) mice, which like primary cells lacking Rel undergo apoptosis in response to antigen receptor ligation, constitutive expression of an A1 transgene inhibits this pathway to cell death. These findings are the first to show that Rel/NF-kappa B regulates physiologically the expression of a Bcl-2-like protein that is critical for the control of cell survival during lymphocyte activation.
Publisher
COLD SPRING HARBOR LAB PRESS
Keywords
NF-KAPPA-B; TUMOR NECROSIS FACTOR; V-REL; ESTROGEN-RECEPTOR; GENE-EXPRESSION; FUSION PROTEIN; BONE-MARROW; DEATH; BCL-2; PHOSPHORYLATION
Terms of Use/Rights Notice
Refer to copyright notice on published article.


Creation Date: 1999-02-15 12:00:00
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