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PMID: 8943845 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Interleukin-2 (IL-2) upregulates BAG-1 gene expression through serine-rich region within IL-2 receptor beta c chain.

Blood ·Vol. 88 ·No. 11 ·1996-12-01 ·Pages 4118-23

Adachi M, Sekiya M, Torigoe T, Takayama S, Reed JC, Miyazaki T, Minami Y, Taniguchi T, Imai K

Abstract

BAG-1 is a Bci-2-binding protein which functions in protection from apoptotic cell death. Here we provide evidence for interleukin-2 (IL-2)-mediated upregulation of BAG-1 expression. In hematopoietic cell line BAF-B03 F7 cells, gene transfer mediated expression of the IL-2R beta c chain is sufficient to confer proliferation and cell survival responses to IL-2. In these IL-2R beta c-expressing cells, BAG-1 mRNA was dramatically induced by IL-2. The IL-2-mediated induction of BAG-1 expression required the activation of tyrosine kinase(s) and was sensitive to rapamycin as the induction of bcl-2 expression was. Analysis of the transfectants which express mutant IL-2R beta c chains or mutant Janus family protein tyrosine kinase Jak3 lacking the kinase domain showed that the IL-2-mediated BAG-1 gene expression required the serinerich region within the IL-2R beta c chain, but Jak3 activation was dispensable. The signaling pathway for BAG-1 gene expression thus highly resembles that for bcl-2 gene expression, strongly suggesting that their induction shares the same signaling pathway. In addition, deletion of the serine-rich region led to loss of IL-2-mediated protection from apoptotic cell death. Taken together, these studies demonstrate that the serine-rich region of the IL-2R beta c chain mediates the coordinated expression of bcl-2 and BAG-1 genes, thereby contributing to suppression of apoptosis.

MeSH Terms
1-(5-Isoquinolinesulfonyl)-2-Methylpiperazine/analogs & derivatives,pharmacology Animals Apoptosis/drug effects,genetics Carrier Proteins/biosynthesis,genetics Cell Line DNA-Binding Proteins Enzyme Inhibitors/pharmacology Gene Expression Regulation/drug effects Genistein Hematopoietic Stem Cells/drug effects,metabolism Humans Interleukin-2/pharmacology Isoflavones/pharmacology Janus Kinase 3 Lymphocytes/drug effects,metabolism Mice Phosphorylation Phytohemagglutinins/pharmacology Polyenes/pharmacology Protein Processing, Post-Translational Protein-Tyrosine Kinases/antagonists & inhibitors,physiology Proto-Oncogene Proteins c-bcl-2/biosynthesis,genetics RNA, Messenger/biosynthesis,genetics Receptors, Interleukin-2/chemistry,drug effects Serine Signal Transduction/drug effects Sirolimus Stimulation, Chemical Tacrolimus/pharmacology Transcription Factors Transfection
Chemicals
BCL2-associated athanogene 1 protein Carrier Proteins DNA-Binding Proteins Enzyme Inhibitors Interleukin-2 Isoflavones Phytohemagglutinins Polyenes Proto-Oncogene Proteins c-bcl-2 RNA, Messenger Receptors, Interleukin-2 Transcription Factors Serine KN 62 1-(5-Isoquinolinesulfonyl)-2-Methylpiperazine Genistein Protein-Tyrosine Kinases JAK3 protein, human Jak3 protein, mouse Janus Kinase 3 Sirolimus Tacrolimus
Authors & Affiliations
9 authors, click to expand affiliations / ORCID
Adachi M
First Department of Internal Medicine, Sapporo Medical University School of Medicine, Japan.
Sekiya M
Torigoe T
Takayama S
Reed J C
Miyazaki T
Minami Y
Taniguchi T
Imai K
Article Info
Journal
Blood
Abbr.
Blood
ISSN
0006-4971
Published
1996-12-01
Pages
4118-23
Language
English
Region
United States
NLM ID
7603509
Subset
IM
Grants
NCI NIH HHS · CA-67329 · United States
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