Three-dimensional reconstruction of the membrane skeleton at the plasma membrane interface by electron tomography

被引:266
作者
Morone, Nobuhiro
Fujiwara, Takahiro
Murase, Kotono
Kasai, Rinshi S.
Ike, Hiroshi
Yuasa, Shigeki
Usukura, Jiro
Kusumi, Akihiro [1 ]
机构
[1] Japan Sci & Technol Agcy, Kusumi Membrane Org Project, Exploratory Res Adv Technol, Nagoya, Aichi 4600012, Japan
[2] Nagoya Univ, Dept Cell Biol & Anat, Grad Sch Med, Nagoya, Aichi 466, Japan
[3] Natl Ctr Neurol & Psychiat, Dept Ultrastruct Res, Natl Inst Neurosci, Tokyo 1878502, Japan
[4] Kyoto Univ, Membrane Mech Project, Int Cooperat Res Project, Japan Sci & Technol Agcy,Inst Frontier Med Sci, Kyoto 6068507, Japan
关键词
D O I
10.1083/jcb.200606007
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Three-dimensional images of the undercoat structure on the cytoplasmic surface of the upper cell membrane of normal rat kidney fibroblast (NRK) cells and fetal rat skin keratinocytes were reconstructed by electron tomography, with 0.85-nm-thick consecutive sections made similar to 100 nm from the cytoplasmic surface using rapidly frozen, deeply etched, platinum-replicated plasma membranes. The membrane skeleton (MSK) primarily consists of actin. laments and associated proteins. The MSK covers the entire cytoplasmic surface and is closely linked to clathrin-coated pits and caveolae. The actin. laments that are closely apposed to the cytoplasmic surface of the plasma membrane ( within 10.2 nm) are likely to form the boundaries of the membrane compartments responsible for the temporary confinement of membrane molecules, thus partitioning the plasma membrane with regard to their lateral diffusion. The distribution of the MSK mesh size as determined by electron tomography and that of the compartment size as determined from high speed single-particle tracking of phospholipid diffusion agree well in both cell types, supporting the MSK fence and MSK-anchored protein picket models.
引用
收藏
页码:851 / 862
页数:12
相关论文
共 68 条
[1]   AGORINS - MAJOR STRUCTURAL PROTEINS OF THE PLASMA-MEMBRANE SKELETON OF P815 TUMOR-CELLS [J].
APGAR, JR ;
MESCHER, MF .
JOURNAL OF CELL BIOLOGY, 1986, 103 (02) :351-360
[2]   Ankyrins and cellular targeting of diverse membrane proteins to physiological sites [J].
Bennett, V ;
Chen, LS .
CURRENT OPINION IN CELL BIOLOGY, 2001, 13 (01) :61-67
[3]   SPECTRIN-BASED MEMBRANE SKELETON - A MULTIPOTENTIAL ADAPTER BETWEEN PLASMA-MEMBRANE AND CYTOPLASM [J].
BENNETT, V .
PHYSIOLOGICAL REVIEWS, 1990, 70 (04) :1029-1065
[4]   INTERACTION OF CYTOSKELETAL PROTEINS ON THE HUMAN-ERYTHROCYTE MEMBRANE [J].
BRANTON, D ;
COHEN, CM ;
TYLER, J .
CELL, 1981, 24 (01) :24-32
[5]   EFFECT OF HYDRODYNAMIC INTERACTIONS ON THE DIFFUSION OF INTEGRAL MEMBRANE-PROTEINS - DIFFUSION IN PLASMA-MEMBRANES [J].
BUSSELL, SJ ;
KOCH, DL ;
HAMMER, DA .
BIOPHYSICAL JOURNAL, 1995, 68 (05) :1836-1849
[6]   THE EFFECT OF HYDRODYNAMIC INTERACTIONS ON THE TRACER AND GRADIENT DIFFUSION OF INTEGRAL MEMBRANE-PROTEINS IN LIPID BILAYERS [J].
BUSSELL, SJ ;
HAMMER, DA ;
KOCH, DL .
JOURNAL OF FLUID MECHANICS, 1994, 258 :167-190
[7]   TRANSFORMATIONS IN STRUCTURE OF CYTOPLASMIC GROUND SUBSTANCE IN ERYTHROPHORES DURING PIGMENT AGGREGATION AND DISPERSION .1. STUDY USING WHOLE-CELL PREPARATIONS IN STEREO HIGH-VOLTAGE ELECTRON-MICROSCOPY [J].
BYERS, HR ;
PORTER, KR .
JOURNAL OF CELL BIOLOGY, 1977, 75 (02) :541-558
[8]   MECHANOCHEMISTRY OF PROTEIN 4.1S SPECTRIN-ACTIN-BINDING DOMAIN - TERNARY COMPLEX INTERACTIONS, MEMBRANE-BINDING, NETWORK INTEGRATION, STRUCTURAL STRENGTHENING [J].
DISCHER, DE ;
WINARDI, R ;
SCHISCHMANOFF, PO ;
PARRA, M ;
CONBOY, JG ;
MOHANDAS, N .
JOURNAL OF CELL BIOLOGY, 1995, 130 (04) :897-907
[9]   LATERAL MOVEMENTS OF MEMBRANE-GLYCOPROTEINS RESTRICTED BY DYNAMIC CYTOPLASMIC BARRIERS [J].
EDIDIN, M ;
KUO, SC ;
SHEETZ, MP .
SCIENCE, 1991, 254 (5036) :1379-1382
[10]  
Fujimoto K, 1996, J CELL SCI, V109, P2453