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PMID: 3509878 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

High affinity interleukin 2 receptors in HTLV-1-infected T cells can mediate signals for gene expression.

Virus genes ·Vol. 1 ·No. 1 ·1987-11-00 ·Pages 35-47

Sakitani M, Nakamura M, Fujii M, Sugamura K, Hinuma Y

Abstract

The expression of transcripts of the c-myb and c-myc protooncogenes and the interleukin 2 receptor (IL-2R) gene in human T cells infected with human T-cell leukemia virus type 1 (HTLV-1) after exposure to interleukin 2 (IL-2) were examined. Infection with HTLV-1 is known to be associated with constitutive expression of IL-2R, although infected cells do not require IL-2 for growth. Northern blot analysis showed that expression of the mRNAs of the c-myb, c-myc, and IL-2R genes were markedly increased by addition of IL-2 into the cultures, indicating that IL-2R transduced signals for gene expression in these cells as in normal T cells. Studies on distinct HTLV-1-infected T cell clones that differed in numbers of high-affinity IL-2R, showed that the extents of increase in mRNA expression by IL-2 were correlated with the number of high-affinity IL-2R. This correlation was confirmed by demonstration that the levels of mRNA expression were proportional to the numbers of IL-2-bound high-affinity but not low-affinity receptors. Thus, the signals induced by IL-2 for gene expression may be through high-affinity IL-2R.

MeSH Terms
Blotting, Northern Cell Line Gene Expression Regulation Human T-lymphotropic virus 1/genetics Humans Interleukin-2/metabolism Kinetics RNA, Messenger/analysis,metabolism Receptors, Interleukin-2/genetics,metabolism Recombinant Proteins/biosynthesis Signal Transduction T-Lymphocytes/metabolism,microbiology
Chemicals
Interleukin-2 RNA, Messenger Receptors, Interleukin-2 Recombinant Proteins
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Sakitani M
Institute for Virus Research, Kyoto University, Japan.
Nakamura M
Fujii M
Sugamura K
Hinuma Y
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Article Info
Journal
Virus genes
Abbr.
Virus Genes
ISSN
0920-8569
Published
1987-11-00
Pages
35-47
Language
English
Region
United States
NLM ID
8803967
Subset
IM
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