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PMID: 3132502 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Protein phosphorylation mediated by IL-2/IL-2 receptor beta-chain interaction.

Journal of immunology (Baltimore, Md. : 1950) ·Vol. 141 ·No. 1 ·1988-07-01 ·Pages 174-9

Ishii T, Takeshita T, Numata N, Sugamura K

Abstract

We previously found that IL-2 rapidly induced protein phosphorylation of a 67-kDa (pp67) and four 63-kDa (pp63s) cellular proteins in various T cells. Here, we show that the IL-2-stimulated phosphorylation is mediated by the IL-2R beta-chain composed of the high affinity IL-2R, and induced by activation of Ca2+/phospholipid-dependent protein kinase C (PKC). The IL-2-stimulated phosphorylation was always observed in various T cell lines bearing high affinity IL-2R, but never observed in cells which express only low affinity IL-2R consisted of alpha-chain alone. When the expression of high affinity IL-2R was modified by anti-IL-2R mAb for reducing the affinity to 8- to 10-fold lower without affecting the sites of IL-2R, the effective dose of IL-2 on phosphorylation of pp67 increased 8 to 10 times. When cells were treated with pronase, approximately 95% sites of low affinity IL-2R were selectively decreased, but the IL-2 dose dependency for pp67 phosphorylation was little affected. These data exactly suggest that protein phosphorylation in response to IL-2 such as pp67 and pp63s, is mediated by high affinity but not low affinity IL-2R. Furthermore, the IL-2-stimulated phosphorylation of these proteins was also observed in MLA 144 cells which express only low affinity IL-2R consisting of beta-chain alone. In addition, various phorbol esters and tumor promoters, which activate PKC, were also demonstrated to induce the phosphorylation of a pp67 and pp63s in these T cell lines. Therefore, the present study suggests that IL-2/IL-2R beta-chain interaction triggers the phosphorylation of pp67 and pp63s, where the PKC may have an important role.

MeSH Terms
Animals Antibodies, Monoclonal/physiology Cell Line Humans Hylobates Interleukin-2/metabolism,physiology Molecular Weight Phosphoproteins/metabolism Phosphorylation Pronase/pharmacology Protein Kinase C/metabolism Receptors, Immunologic/immunology,physiology Receptors, Interleukin-2 T-Lymphocytes/metabolism
Chemicals
Antibodies, Monoclonal Interleukin-2 Phosphoproteins Receptors, Immunologic Receptors, Interleukin-2 Protein Kinase C Pronase
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Ishii T
Department of Bacteriology, Tohoku University School of Medicine, Sendai, Japan.
Takeshita T
Numata N
Sugamura K
Article Info
Journal
Journal of immunology (Baltimore, Md. : 1950)
Abbr.
J Immunol
ISSN
0022-1767
Published
1988-07-01
Pages
174-9
Language
English
Region
United States
NLM ID
2985117R
Subset
IM
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