FEBS Letters
Volume 582, Issue 27 , Pages 3711-3718, 12 November 2008

Lipid rafts and T-lymphocyte function: Implications for autoimmunity

Edited by Sandro Sonnino

  • Panagiotis S. Kabouridis

      Affiliations

    • William Harvey Research Institute, Queen Mary’s School of Medicine & Dentistry, University of London, Charterhouse Square, London EC1M 6BQ, United Kingdom
    • Corresponding Author InformationCorresponding author. Fax: +44 (0) 20 7882 6076.
  • ,
  • Elizabeth C. Jury

      Affiliations

    • Centre for Rheumatology, Royal Free & University College Medical School, University College London, London W1P 4JF, United Kingdom

Received 4 September 2008; received in revised form 6 October 2008; accepted 7 October 2008. published online 17 October 2008.

Abstract 

Experimental evidence indicates that the mammalian cell membrane is compartmentalized. A structural feature that supports membrane segmentation implicates assemblies of selected lipids broadly referred to as lipid rafts. In T-lymphocytes, lipid rafts are implicated in signalling from the T-cell antigen receptor (TCR) and in localization and function of proteins residing proximal to the receptor. This review summarizes the current literature that deals with lipid raft involvement in T-cell activation and places particular emphasis in recent studies investigating lipid rafts in autoimmunity. The potential of lipid rafts as targets for the development of a new class of immune-modulating compounds is discussed.

Keywords: Lipid raft, T-cell receptor, Autoimmunity

To access this article, please choose from the options below

Login to an existing account or Register a new account.

  • Purchase this article for 31.50 USD (You must login/register to purchase this article)

    Online access for 24 hours. The PDF version can be downloaded as your permanent record.

  • Subscribe to this title

    Get unlimited online access to this article and all other articles in this title 24/7 for one year.

  • Claim access now

    For current subscribers with Society Membership or Account Number.

  • Visit SciVerse ScienceDirect to see if you have access via your institution.
 

PII: S0014-5793(08)00816-8

doi:10.1016/j.febslet.2008.10.006

FEBS Letters
Volume 582, Issue 27 , Pages 3711-3718, 12 November 2008