Nanoclustering as a dominant feature of plasma membrane organization

被引:214
作者
Garcia-Parajo, Maria F. [1 ,2 ]
Cambi, Alessandra [3 ,4 ,5 ]
Torreno-Pina, Juan A. [1 ]
Thompson, Nancy [6 ]
Jacobson, Ken [7 ,8 ]
机构
[1] ICFO Inst Ciencies Foton, Castelldefels 08860, Barcelona, Spain
[2] Inst Catalana Recerca & Estudis Avancats, Barcelona 08010, Spain
[3] Univ Twente, MIRA Inst Biomed Technol & Tech Med, NL-7522 NB Enschede, Netherlands
[4] Univ Twente, MESA Inst Nanotechnol, NL-7522 NB Enschede, Netherlands
[5] Radboud Univ Nijmegen, Radboud Inst Mol Life Sci, Dept Tumor Immunol, Med Ctr, NL-6500 HB Nijmegen, Netherlands
[6] Univ N Carolina, Dept Chem, Chapel Hill, NC 27599 USA
[7] Univ N Carolina, Dept Cell Biol & Physiol, Chapel Hill, NC 27599 USA
[8] Univ N Carolina, Lineberger Canc Res Ctr, Chapel Hill, NC 27599 USA
关键词
Plasma membrane; Protein nanoclustering; Super-resolution microscopy; GPI-ANCHORED PROTEINS; CELL ANTIGEN RECEPTOR; C-TYPE LECTIN; SINGLE-MOLECULE TRACKING; FC-EPSILON-RI; DC-SIGN; LIPID RAFTS; INFLUENZA HEMAGGLUTININ; NANOSCALE ORGANIZATION; H-RAS;
D O I
10.1242/jcs.146340
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Early studies have revealed that some mammalian plasma membrane proteins exist in small nanoclusters. The advent of super-resolution microscopy has corroborated and extended this picture, and led to the suggestion that many, if not most, membrane proteins are clustered at the plasma membrane at nanoscale lengths. In this Commentary, we present selected examples of glycosylphosphatidyl-anchored proteins, Ras family members and several immune receptors that provide evidence for nanoclustering. We advocate the view that nanoclustering is an important part of the hierarchical organization of proteins in the plasma membrane. According to this emerging picture, nanoclusters can be organized on the mesoscale to form microdomains that are capable of supporting cell adhesion, pathogen binding and immune cell-cell recognition amongst other functions. Yet, a number of outstanding issues concerning nanoclusters remain open, including the details of their molecular composition, biogenesis, size, stability, function and regulation. Notions about these details are put forth and suggestions are made about nanocluster function and why this general feature of protein nanoclustering appears to be so prevalent.
引用
收藏
页码:4995 / 5005
页数:11
相关论文
共 80 条
[1]   Protein oligomerization: How and why [J].
Ali, MH ;
Imperiali, B .
BIOORGANIC & MEDICINAL CHEMISTRY, 2005, 13 (17) :5013-5020
[2]   Cell biology - A role for lipid shells in targeting proteins to caveolae, rafts, and other lipid domains [J].
Anderson, RGW ;
Jacobson, K .
SCIENCE, 2002, 296 (5574) :1821-1825
[3]   Galectin-1 is a novel structural component and a major regulator of H-Ras nanoclusters [J].
Belanis, Liron ;
Plowman, Sarah J. ;
Rotblat, Barak ;
Hancock, John F. ;
Kloog, Yoel .
MOLECULAR BIOLOGY OF THE CELL, 2008, 19 (04) :1404-1414
[4]   Microdomains of the C-type lectin DC-SIGN are portals for virus entry into dendritic cells [J].
Cambi, A ;
de Lange, F ;
van Maarseveen, NM ;
Nijhuis, M ;
Joosten, B ;
van Dijk, EMHP ;
de Bakker, BI ;
Fransen, JAM ;
Bovee-Geurts, PHM ;
van Leeuwen, FN ;
Van Hulst, NF ;
Figdor, CG .
JOURNAL OF CELL BIOLOGY, 2004, 164 (01) :145-155
[5]   Organization of the integrin LFA-1 in nanoclusters regulates its activity [J].
Cambi, Alessandra ;
Joosten, Ben ;
Koopman, Marjolein ;
de Lange, Frank ;
Beeren, Inge ;
Torensma, Ruurd ;
Fransen, Jack A. ;
Garcia-Parajo, Maria ;
van Leeuwen, Frank N. ;
Figdor, Carl G. .
MOLECULAR BIOLOGY OF THE CELL, 2006, 17 (10) :4270-4281
[6]   Signalling complexes and clusters: functional advantages and methodological hurdles [J].
Cebecauer, Marek ;
Spitaler, Martin ;
Serge, Arnauld ;
Magee, Anthony I. .
JOURNAL OF CELL SCIENCE, 2010, 123 (03) :309-320
[7]   Transient anchorage of cross-linked glycosyl-phosphatidylinositol-anchored proteins depends on cholesterol, Src family kinases, caveolin, and phosphoinositides [J].
Chen, Yun ;
Thelin, William R. ;
Yang, Bing ;
Milgram, Sharon L. ;
Jacobson, Ken .
JOURNAL OF CELL BIOLOGY, 2006, 175 (01) :169-178
[8]   The transmembrane protein CBP plays a role in transiently anchoring small clusters of Thy-1, a GPI-anchored protein, to the cytoskeleton [J].
Chen, Yun ;
Veracini, Laurence ;
Benistant, Christine ;
Jacobson, Ken .
JOURNAL OF CELL SCIENCE, 2009, 122 (21) :3966-3972
[9]   Nanoscale organization of the pathogen receptor DC-SIGN mapped by single-molecule high-resolution fluorescence microscopy [J].
de Bakker, Baerbel I. ;
de lange, Frank ;
Cambi, Alessandra ;
Korterik, Jeroen P. ;
van Dijk, Erik M. H. P. ;
van Hulst, Niek F. ;
Figdor, Carl G. ;
Garcia-Parajo, Maria F. .
CHEMPHYSCHEM, 2007, 8 (10) :1473-1480
[10]   Tetraspanin CD82 controls the association of cholesterol-dependent microdomains with the actin cytoskeleton in T lymphocytes: relevance to co-stimulation [J].
Delaguillaumie, A ;
Harriague, J ;
Kohanna, S ;
Bismuth, G ;
Rubinstein, E ;
Seigneuret, M ;
Conjeaud, H .
JOURNAL OF CELL SCIENCE, 2004, 117 (22) :5269-5282