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PMID: 8372354 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

IRS-1: essential for insulin- and IL-4-stimulated mitogenesis in hematopoietic cells.

Science (New York, N.Y.) ·Vol. 261 ·No. 5128 ·1993-09-17 ·Pages 1591-4

Wang LM, Myers MG, Sun XJ, Aaronson SA, White M, Pierce JH

Abstract

Although several interleukin-3 (IL-3)-dependent cell lines proliferate in response to IL-4 or insulin, the 32D line does not. Insulin and IL-4 sensitivity was restored to 32D cells by expression of IRS-1, the principal substrate of the insulin receptor. Although 32D cells possessed receptors for both factors, they lacked the IRS-1--related protein, 4PS, which becomes phosphorylated by tyrosine in insulin- or IL-4--responsive lines after stimulation. These results indicate that factors that bind unrelated receptors can use similar mitogenic signaling pathways in hematopoietic cells and that 4PS and IRS-1 are functionally similar proteins that are essential for insulin- and IL-4--induced proliferation.

MeSH Terms
Animals Cell Division/drug effects Cell Line Hematopoietic Stem Cells/cytology,drug effects Insulin/pharmacology Insulin Receptor Substrate Proteins Interleukin-4/pharmacology Phosphoproteins/metabolism Phosphorylation Receptor, Insulin/metabolism Receptors, Interleukin-4 Receptors, Mitogen/metabolism Transfection Tyrosine/metabolism
Chemicals
Insulin Insulin Receptor Substrate Proteins Phosphoproteins Receptors, Interleukin-4 Receptors, Mitogen Interleukin-4 Tyrosine Receptor, Insulin
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Wang L M
Laboratory of Cellular and Molecular Biology, National Cancer Institute, Bethesda, MD 20892.
Myers M G
Sun X J
Aaronson S A
White M
Pierce J H
Article Info
Journal
Science (New York, N.Y.)
Abbr.
Science
ISSN
0036-8075
Published
1993-09-17
Pages
1591-4
Language
English
Region
United States
NLM ID
0404511
Subset
IM
Grants
NIDDK NIH HHS · DK-43808 · United States
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