Inhibition of protein palmitoylation, raft localization, and T cell signaling by 2-bromopalmitate and polyunsaturated fatty acids Journal Article


Authors: Webb, Y.; Hermida-Matsumoto, L.; Resh, M. D.
Article Title: Inhibition of protein palmitoylation, raft localization, and T cell signaling by 2-bromopalmitate and polyunsaturated fatty acids
Abstract: The ability of the Src family kinases Fyn and Lck to participate in signaling through the T cell receptor is critically dependent on their dual fatty acylation with myristate and palmitate. Here we identify a palmitate analog, 2-bromopalmitate, that effectively blocks Fyn fatty acylation in general and palmitoylation in particular. Treatment of COS-1 cells with 2- bromopalmitate blocked myristoylation and palmitoylation of Fyn and inhibited membrane binding and localization of Fyn to detergent-resistant membranes (DRMs). In Jurkat T cells, 2-bromopalmitate blocked localization of the endogenous palmitoylated proteins Fyn, Lck, and LAT to DRMs. This resulted in impaired signaling through the T cell receptor as evidenced by reductions in tyrosine phosphorylation, calcium release, and activation of mitogen- activated protein kinase. We also examined the ability of long chain polyunsaturated fatty acids (PUFAs) to inhibit protein fatty acylation. PUFAs have been reported to inhibit T cell signaling by excluding Src family kinases from DRMs. Here we show that the PUFAs arachidonic acid and eicosapentaenoic acid inhibit Fyn palmitoylation and consequently block Fyn localization to DRMs. We propose that inhibition of protein palmitoylation represents a novel mechanism by which PUFAs exert their immunosuppressive effects.
Keywords: signal transduction; mitogen activated protein kinase; proto-oncogene proteins; nonhuman; t-lymphocytes; animal cell; animals; enzyme activation; cos cells; animalia; t lymphocyte receptor; protein processing, post-translational; cell fractionation; mitogen-activated protein kinases; src-family kinases; arachidonic acid; t lymphocyte activation; biological transport; jurkat cells; acylation; palmitoylation; icosapentaenoic acid; proto-oncogene proteins c-fyn; calcium mobilization; palmitic acid; palmitates; lymphocyte specific protein tyrosine kinase p56(lck); polyunsaturated fatty acid; fatty acids, unsaturated; 2 bromopalmitic acid; humans; priority journal; article; cell compartmentation
Journal Title: Journal of Biological Chemistry
Volume: 275
Issue: 1
ISSN: 0021-9258
Publisher: American Society for Biochemistry and Molecular Biology  
Date Published: 2000-01-07
Start Page: 261
End Page: 270
Language: English
DOI: 10.1074/jbc.275.1.261
PUBMED: 10617614
PROVIDER: scopus
DOI/URL:
Notes: Export Date: 18 November 2015 -- Source: Scopus
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  1. Yael Webb
    4 Webb
  2. Marilyn D Resh
    120 Resh