Plasma membrane reorganization: A glycolipid gateway for microbes

被引:51
|
作者
Aigal, Sahaja [1 ,2 ,3 ]
Claudinon, Julie [1 ,2 ]
Roemer, Winfried [1 ,2 ]
机构
[1] Univ Freiburg, Fac Biol, D-79104 Freiburg, Germany
[2] Univ Freiburg, BIOSS Ctr Biol Signaling Studies, D-79104 Freiburg, Germany
[3] Int Max Planck Res Sch Mol & Cellular Biol IMPRS, Max Planck Inst Immunobiol & Epigenet, D-79108 Freiburg, Germany
来源
基金
欧洲研究理事会;
关键词
Toxin; Virus; Bacterium; Receptor clustering; Membrane invagination; Lipid rafts; ATOMIC-FORCE MICROSCOPY; MUTANT CHOLERA-TOXIN; PSEUDOMONAS-AERUGINOSA; SHIGA TOXIN; LIPID RAFTS; GLOBOTRIAOSYL CERAMIDE; LISTERIA-MONOCYTOGENES; MOLECULAR PATHOGENESIS; MEDIATED ENDOCYTOSIS; ACTIN POLYMERIZATION;
D O I
10.1016/j.bbamcr.2014.11.014
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Ligand-receptor interactions, which represent the core for cell signaling and internalization processes are largely affected by the spatial configuration of host cell receptors. There is a growing piece of evidence that receptors are not homogeneously distributed within the plasma membrane, but are rather pre-clustered in nanodomains, or clusters are formed upon ligand binding. Pathogens have evolved many strategies to evade the host immune system and to ensure their survival by hijacking plasma membrane receptors that are most often associated with lipid rafts. In this review, we discuss the early stage molecular and physiological events that occur following ligand binding to host cell glycolipids. The ability of various biological ligands (e.g. toxins, lectins, viruses or bacteria) that bind to glycolipids to induce their own uptake into mammalian cells by creating negative membrane curvature and membrane invaginations is explored. We highlight recent trends in understanding nanoscale plasma membrane (re-)organization and present the benefits of using synthetic membrane systems. This article is part of a Special Issue entitled: Nanoscale membrane organisation and signalling. (C) 2014 Elsevier B.V. All rights reserved.
引用
下载
收藏
页码:858 / 871
页数:14
相关论文
共 50 条
  • [31] The Importance of Glycolipid Crosslinking in Altering the Membrane Curvature
    Kabbani, Abir
    Raghunathan, Krishnan
    Kenworthy, Anne
    Lencer, Wayne
    Kelly, Christopher V.
    BIOPHYSICAL JOURNAL, 2019, 116 (03) : 165A - 165A
  • [32] Glycolipid Biotinylation on Purple Membrane with Maintained Bioactivity
    Xiang, Yan
    Yang, Meng
    Su, Tao
    Chen, Yuanyuan
    Bi, Lijun
    Hu, Kunsheng
    JOURNAL OF PHYSICAL CHEMISTRY B, 2009, 113 (22): : 7762 - 7766
  • [33] THE GLYCOLIPID ANCHOR OF MEMBRANE-SURFACE PROTEINS
    ROSSE, WF
    SEMINARS IN HEMATOLOGY, 1993, 30 (03) : 219 - 231
  • [34] Membrane interaction and activity of the glycolipid transfer protein
    West, G.
    Nylund, M.
    Slotte, J. P.
    Mattjus, P.
    CHEMISTRY AND PHYSICS OF LIPIDS, 2006, 143 (1-2) : 97 - 98
  • [35] Key contributions of a glycolipid to membrane protein integration
    Shimamoto, Keiko
    Fujikawa, Kohki
    Osawa, Tsukiho
    Mori, Shoko
    Nomura, Kaoru
    Nishiyama, Ken-ichi
    PROCEEDINGS OF THE JAPAN ACADEMY SERIES B-PHYSICAL AND BIOLOGICAL SCIENCES, 2024, 100 (07): : 387 - 413
  • [36] The translocon: A dynamic gateway at the ER membrane
    Johnson, AE
    van Waes, MA
    ANNUAL REVIEW OF CELL AND DEVELOPMENTAL BIOLOGY, 1999, 15 : 799 - 842
  • [37] Glycosyltransferase microarray displayed on the glycolipid LB membrane
    Nagahori, N
    Niikura, K
    Sadamoto, R
    Taniguchi, M
    Yamagishi, A
    Monde, K
    Nishimura, SI
    ADVANCED SYNTHESIS & CATALYSIS, 2003, 345 (6-7) : 729 - 734
  • [38] Nanoscale Analysis of Glycolipid Distribution in the Cell Membrane
    Fujita, Akikazu
    Fujimoto, Toyoshi
    TRENDS IN GLYCOSCIENCE AND GLYCOTECHNOLOGY, 2010, 22 (126-28) : 173 - 181
  • [39] GLYCOLIPID-ANCHORED MEMBRANE-PROTEINS
    BRON, C
    FASEL, N
    BULLETIN DE L INSTITUT PASTEUR, 1991, 89 (01): : 59 - 69
  • [40] Membrane interaction and activity of the glycolipid transfer protein
    West, Gun
    Nylund, Matts
    Slotte, J. Peter
    Mattjus, Peter
    BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 2006, 1758 (11): : 1732 - 1742