| Literature DB >> 25759911 |
Noel M Rysavy1, Lori M N Shimoda, Alyssa M Dixon, Mark Speck, Alexander J Stokes, Helen Turner, Eric Y Umemoto.
Abstract
Loss of plasma membrane asymmetry is a hallmark of apoptosis, but lipid bilayer asymmetry and loss of asymmetry can contribute to numerous cellular functions and responses that are independent of programmed cell death. Exofacial exposure of phosphatidylserine occurs in lymphocytes and mast cells after antigenic stimulation and in the absence of apoptosis, suggesting that there is a functional requirement for phosphatidylserine exposure in immunocytes. In this review we examine current ideas as to the nature of this functional role in mast cell activation. Mechanistically, there is controversy as to the candidate proteins responsible for phosphatidylserine translocation from the internal to external leaflet, and here we review the candidacies of mast cell PLSCR1 and TMEM16F. Finally we examine the potential relationship between functionally important mast cell membrane perturbations and phosphatidylserine exposure during activation.Entities:
Keywords: ABCA, ABC binding cassette family A; CRAC, calcium release activated channel; GPMV, giant plasma membrane vesicle; ITIM, immunoreceptor tyrosine based inhibitory motif; PLA2, phospholipase A2; PLSCR, phospholipid scramblase; PMA, phorbol 12,13-myristate acetate; RBL, rat basophilic leukemia; RFU, relative fluorescence units; ROI, region of interest; TMEM, transmembrane protein; TMEM16F; WGA, wheat germ agglutinin; mast cells; membrane lipids; phosphatidylserine
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Year: 2014 PMID: 25759911 PMCID: PMC4914033 DOI: 10.1080/19490992.2014.995516
Source DB: PubMed Journal: Bioarchitecture ISSN: 1949-0992