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PMID: 2984341 Published · ppublish English Comparative Study Journal Article Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

T cell growth factor required for optimal induction of T cell growth factor receptor expression in phytohemagglutinin-stimulated T cells.

Journal of biological response modifiers ·Vol. 4 ·No. 1 ·1985-02-00 ·Pages 83-95

Reeves WG, Zamkoff KW, Poiesz BJ, Paolozzi FP, Tomar RH, Moore JL, Ruscetti FW

Abstract

Proliferation of normal human T cells in vitro requires activation of resting T cells by lectin or antigen. This stimulation initiates a series of events which includes elaboration of T cell growth factor (TCGF), expression of TCGF receptors, and, ultimately, cellular proliferation. We sought to determine if TCGF was required for expression of the TCGF receptor in phytohemagglutinin (PHA)-stimulated normal human T cells. Utilizing dexamethasone (DEX), a known inhibitor of TCGF production, reductions in T cell proliferation, TCGF production, and TCGF receptor expression, as measured by TCGF adsorption and Tac acquisition, were demonstrated after PHA stimulation. When exogenous partially purified TCGF was added to DEX-containing cultures, the DEX inhibition of proliferation and TCGF receptor expression was completely reversed. These experiments were reproduced utilizing both highly purified TCGF from the Jurkat cell line and purified TCGF synthesized by bacteria from cloned TCGF DNA. Short-term experiments showed TCGF to be capable of restoring Tac antigen expression after DEX inhibition in the absence of cellular proliferation. These results indicate that TCGF is required for optimal expression of Tac antigen-associated TCGF receptors in PHA-activated T cells.

MeSH Terms
Antigens, Surface Dexamethasone/pharmacology Humans In Vitro Techniques Interleukin-2/biosynthesis,immunology Lymphocyte Activation/drug effects Phytohemagglutinins/pharmacology Receptors, Immunologic/biosynthesis Receptors, Interleukin-2 T-Lymphocytes/immunology Tumor Necrosis Factor Receptor Superfamily, Member 7
Chemicals
Antigens, Surface Interleukin-2 Phytohemagglutinins Receptors, Immunologic Receptors, Interleukin-2 Tumor Necrosis Factor Receptor Superfamily, Member 7 Dexamethasone
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Reeves W G
Zamkoff K W
Poiesz B J
Paolozzi F P
Tomar R H
Moore J L
Ruscetti F W
Article Info
Journal
Journal of biological response modifiers
Abbr.
J Biol Response Mod
ISSN
0732-6580
Published
1985-02-00
Pages
83-95
Language
English
Region
United States
NLM ID
8219656
Subset
IM
Grants
NCI NIH HHS · LR23CA32800-01 EI · United States
External Links
PubMed source
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