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PMID: 6197462 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Modulation of cell-mediated cytotoxicity function after alteration of fatty acid composition in vitro.

Journal of immunology (Baltimore, Md. : 1950) ·Vol. 132 ·No. 1 ·1984-01-00 ·Pages 81-7

Bialick R, Gill R, Berke G, Clark WR

Abstract

Fatty acids incorporated into cytotoxic T lymphocytes (CTL) during in vitro stimulation can enhance or inhibit the subsequent expression of cell-mediated cytotoxicity, depending on the class of fatty acid. Unsaturated fatty acids enhance cytolysis, whereas saturated fatty acids inhibit it. The effects of fatty acids on cytolysis can be mediated in the absence of cell division, thus eliminating relative clonal amplification or contraction as a basis for the observed effects. Nevertheless, the net result of fatty acid alteration is an increase (unsaturated fatty acids) or decrease (saturated fatty acids) in the frequency, in the treated immune population, of CTL capable of lysing target cells. These observations are best explained by a model in which fatty acid incorporated into cell membrane phospholipids results in a direct recruitment into or out of the pool of CTL within the immune population capable of lysing target cells under the conditions employed to assay cytotoxicity.

MeSH Terms
Animals Cell Count Cell Division Cytotoxicity Tests, Immunologic/methods Cytotoxicity, Immunologic/drug effects Epitopes Fatty Acids, Nonesterified/metabolism,pharmacology Female Immunity, Cellular Immunologic Memory Lymphocyte Activation Mice Mice, Inbred BALB C Mice, Inbred C57BL Mice, Inbred DBA T-Lymphocytes, Cytotoxic/immunology,metabolism
Chemicals
Epitopes Fatty Acids, Nonesterified
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Bialick R
Gill R
Berke G
Clark W R
Article Info
Journal
Journal of immunology (Baltimore, Md. : 1950)
Abbr.
J Immunol
ISSN
0022-1767
Published
1984-01-00
Pages
81-7
Language
English
Region
United States
NLM ID
2985117R
Subset
IM
Grants
PHS HHS · 14747 · United States
NCI NIH HHS · 3T32 CA 09030 · United States
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