Overexpression of RelA Causes G1 Arrest and Apoptosis in a Pro-B Cell Line
NF-κB/Rel family proteins form a network of post-translationally regulated transcription factors that respond to a variety of extracellular stimuli and mediate distinct cellular responses. These responses include cytokine gene expression, regulated cell cycle activation, and both the protection fro...
Saved in:
Published in | The Journal of biological chemistry Vol. 274; no. 13; pp. 8708 - 8716 |
---|---|
Main Authors | , |
Format | Journal Article |
Language | English |
Published |
United States
American Society for Biochemistry and Molecular Biology
26.03.1999
|
Subjects | |
Online Access | Get full text |
Cover
Loading…
Summary: | NF-κB/Rel family proteins form a network of post-translationally regulated transcription factors that respond to a variety
of extracellular stimuli and mediate distinct cellular responses. These responses include cytokine gene expression, regulated
cell cycle activation, and both the protection from and induction of the cell death program. To examine the function of individual
Rel family proteins in B cell development and resolve their role in the signaling of apoptosis, we used a tetracycline-regulated
gene expression system to overexpress either c-Rel or RelA in the transformed pro-B cell line 220-8. Elevated levels of RelA,
but not c-Rel, induced a G 1 cell cycle arrest followed by apoptosis. Both the DNA binding and transactivation domains of RelA were required for this
effect. When RelA was overexpressed in the immature B cell line WEHI 231 or the mature B cell line M12, neither cell cycle
arrest nor apoptosis was evident. The differential effects of elevated RelA levels in these cell lines suggests that susceptibility
to NF-κB-induced apoptosis may reflect a relevant selection event during B cell development. |
---|---|
ISSN: | 0021-9258 1083-351X |
DOI: | 10.1074/jbc.274.13.8708 |