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PMID: 2783601 Published · ppublish English Journal Article

Derivation of a T cell line that is highly responsive to IL-4 and IL-2 (CT.4R) and of an IL-2 hyporesponsive mutant of that line (CT.4S).

Journal of immunology (Baltimore, Md. : 1950) ·Vol. 142 ·No. 3 ·1989-02-01 ·Pages 800-7

Hu-Li J, Ohara J, Watson C, Tsang W, Paul WE

Abstract

The derivation of subline of CTLL cells that grow in IL-4/B cell stimulatory factor-1 is described. These cells, designated CT.4R cells, were obtained by extended culture of the CTLL line CT.EV in IL-4. CT.4R cells are highly responsive to both IL-4 and IL-2. Mutagenesis of CT.4R cells with ethylmethane sulfonate and selection for lack of expression of the p55 chain of the IL-2R was carried out and a clone was selected that was hyporesponsive to IL-2 but retained full sensitivity to IL-4. These cells, designated CT.4S cells, develop a very meager response to IL-2 at concentrations of 100 U/ml or less although that display vigorous responses to higher IL-2 concentrations. CT.4S cells give measurable responses to 3-10 U/ml (approximately 15-50 pg/ml) of IL-4. CT.4R and CT.4S cells fail to respond to IL-1, IL-3, IL-6, granulocyte-macrophage-CSF, granulocyte-CSF, CSF-1 or IFN-gamma. Thus, CT.4S cells can be used as a sensitive and specific bioassay for IL-4. ID CT.4R cells can be grown in either IL-4 or IL-2. When grown in IL-4, CT.4R cells express small amounts of the p55 chain of the IL-2R but rapidly upregulate their level of expression of p55 when IL-2 is added and rapidly diminish p55 expression when IL-2 is removed. Thus, although IL-2 and IL-4 both stimulate vigorous growth responses by CT.4R cells, they differ in their capacity to induce the expression of the p55 chain implying that their mechanisms of T cell stimulation are not identical.

MeSH Terms
Cell Line Dose-Response Relationship, Immunologic Drug Synergism Humans Interleukin-2/metabolism,pharmacology Interleukin-4 Interleukins/metabolism,pharmacology Lymphocyte Activation/drug effects Mutation Receptors, Interleukin-2/drug effects,immunology,metabolism T-Lymphocytes, Cytotoxic/drug effects,immunology,metabolism
Chemicals
Interleukin-2 Interleukins Receptors, Interleukin-2 Interleukin-4
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Hu-Li J
Laboratory of Immunology, National Institute of Allergy and Infectious Diseases, Bethesda, MD 20892.
Ohara J
Watson C
Tsang W
Paul W E
Article Info
Journal
Journal of immunology (Baltimore, Md. : 1950)
Abbr.
J Immunol
ISSN
0022-1767
Published
1989-02-01
Pages
800-7
Language
English
Region
United States
NLM ID
2985117R
Subset
IM
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