Journal
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
Volume 99, Issue 15, Pages 9830-9835Publisher
NATL ACAD SCIENCES
DOI: 10.1073/pnas.152571899
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- NCI NIH HHS [T32 CA09140, T32 CA009140] Funding Source: Medline
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An oligonucleotide-based microarray analysis of 9,500 genes and expressed sequence tags (ESTs) demonstrated that the type 1 inositol 1,4,5-trisphosphate receptor (IP3R) was significantly down-regulated in Bcl-X-L-expressing as compared with control cells. This result was confirmed at the mRNA and protein levels by Northern and Western blot analyses of two independent hematopoietic cell lines and murine primary T cells. Bcl-X-L expression resulted in a dose-dependent decrease in IP3R protein. IP3R expression is regulated as part of a mitochondrion-to-nucleus stress-responsive pathway. The uncoupling of mitochondrial oxidative phosphorylation resulted in induction of binding of the transcription factor NFATc2 to the IP3R promoter and transcriptional activation of IP3R. Expression of Bcl-XL led to a decreased induction of both NFATc2 DNA binding to the IP3R promoter and IP3R expression in response to the inhibition of mitochondrial oxidative phosphorylation. The Bcl-X-L-dependent decrease in IP3R expression also correlated with a reduced T cell antigen receptor ligation-induced Ca2+ flux in Bcl-XL transgenic murine T cells, and microsomal vesicles prepared from BCl-X-L-overexpressing cells exhibited lower IN-mediated Ca2+ release capacity. Furthermore, reintroducing IP3R into Bcl-X-L-transfected cells partially reversed Bcl-X-L-dependent anti-apoptotic activity. These results suggest that even under non-apoptotic conditions, expression of Bcl-2-family proteins influences a signaling network that links changes in mitochondrial metabolism to alterations in nuclear gene expression.
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