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PMID: 9846704 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Defective IL-2-mediated IL-2 receptor alpha chain expression in Stat3-deficient T lymphocytes.

International immunology ·Vol. 10 ·No. 11 ·1998-11-00 ·Pages 1747-51

Akaishi H, Takeda K, Kaisho T, Shineha R, Satomi S, Takeda J, Akira S

Abstract

Stat3, a member of signal transducers and activators of transcription (STAT), is activated by a variety of cytokines. Recently, mice lacking Stat3 specifically in T cells have been generated and shown to be defective in IL-6-induced proliferation due to the impairment in IL-6-mediated prevention of apoptosis. In the present study, we show that Stat3-deficient T cells are partially defective in IL-2-induced proliferation. Stat3-deficient T cells show impaired IL-2-mediated IL-2 receptor (IL-2R) alpha chain expression. When Stat3-deficient T cells are stimulated with high-dose IL-2, these T cells express IL-2Ralpha and proliferate to similar extents as wild-type T cells. These demonstrate that Stat3 activation is required for efficient T cell proliferation by IL-2 through IL-2Ralpha induction. Taken together, these findings demonstrate that Stat3 activation in T cells is responsible for IL-2- and IL-6-induced proliferation through distinct mechanisms.

MeSH Terms
Animals Apoptosis DNA-Binding Proteins/physiology Interleukin-2/pharmacology Lymphocyte Activation/drug effects Mice Milk Proteins Receptors, Interleukin-2/biosynthesis STAT3 Transcription Factor STAT5 Transcription Factor Signal Transduction T-Lymphocytes/cytology,immunology,metabolism Trans-Activators/physiology
Chemicals
DNA-Binding Proteins Interleukin-2 Milk Proteins Receptors, Interleukin-2 STAT3 Transcription Factor STAT5 Transcription Factor Stat3 protein, mouse Trans-Activators
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Akaishi H
Department of Biochemistry, Hyogo College of Medicine, Nishinomiya, Japan.
Takeda K
Kaisho T
Shineha R
Satomi S
Takeda J
Akira S
Article Info
Journal
International immunology
Abbr.
Int Immunol
ISSN
0953-8178
Published
1998-11-00
Pages
1747-51
Language
English
Region
England
NLM ID
8916182
Subset
IM
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