Medical Journals

Phosphatidylserine Exposure in B Lymphocytes: a Role for Lipid Packing.

Authors:
  • Elliott James I
  • Sardini Alessandro
  • Cooper Joanne C
  • Alexander Denis R
  • Davanture Suzel
  • Chimini Giovanna
  • Higgins Christopher F

From: Medical Research council (MRC) Clinical Sciences Centre, Faculty of Medicine, Imperial College, Hammersmith Hospital Campus, Du Cane Rd, London, W12 0NN, United Kingdom. james.elliott@csc.mrc.ac.uk

Blood

  • Publish Date: Sep 2006
  • ISSN: 0006-4971
  • Volume: 108
  • Issue: 5
  • Pages: 1611-7
  • Medium: Print
  • Language: English
  • Citation (JAMA): Elliott James I, Sardini Alessandro, Cooper Joanne C, et al. Phosphatidylserine Exposure in B Lymphocytes: a Role for Lipid Packing.. Blood Sep 2006;108:1611-7

Abstract

Plasma membrane lipids are usually distributed asymmetrically, with phosphatidylserine (PS) confined to the inner leaflet. PS exposure at the outer leaflet occurs early in apoptosis, but it is also constitutive on some nonapoptotic cell populations where it plays a role in cell signaling. How PS is transported (“flopped”) to the cell surface is unknown. Contrary to previous reports that normal murine B lymphocytes lack lipid asymmetry, we show that PS is normally restricted to the inner leaflet of these cells. PS exposure on normal B cells did, however, occur spontaneously ex vivo. Consistent with the hypothesis that loss of PS asymmetry is regulated by CD45, PS is constitutively exposed on viable, CD45-deficient B cells. We show that calcium-stimulated PS exposure in B cells is strain variable, ABCA1 independent, and both preceded by and dependent on a decrease in lipid packing. This decrease in lipid packing is concomitant with cell shrinkage and consequent membrane distortion, both of which are potently inhibited by blockers of volume-regulatory K+ and Cl- ion channels. Thus, changes in plasma membrane organization precede PS translocation. The data suggest a model in which PS redistribution may occur by a translocase-independent mechanism at energetically favorable sites of membrane perturbation where lipid packing is decreased.

Mesh Headings (Keywords): Animals, B-Lymphocytes, Biological Transport, Flow Cytometry, Lipids, Lymphocyte Activation, Mice, Mice, Inbred C57BL, Phosphatidylinositols


Check for Full Text / PubMed Unique Identifier (PMID): 16684961


This abstract is part of PubMed, a service of the U.S. National Library of Medicine. PubMed includes more than 17 million citations from MEDLINE and other life science journals for biomedical articles. See Copyright and Disclaimers.

Linked medical terms appearing on this page are added by Healia to help readers find more information and are not part of the original PubMed document.

The data herein was last updated on July 8th, 2008 and may not reflect the most current and accurate data available from NLM.


Advertisements

About | Privacy Policy | Business Solutions | Advertise | Contact | Add Healia to your site

©2012. Healia / Meredith Corporation  

Use of this site constitutes acceptance of our Terms of Service and Privacy Policy. All content on this Web site, including medical opinion and any other health-related information, is for informational purposes only and should not be used for a specific diagnosis or individual treatment plan for any situation. Use of this site and the information contained herein does not create a doctor-patient relationship. Always seek the direct advice of your doctor in connection with any questions or issues you may have regarding your own health or the health of others.