Membrane segregation and downregulation of raft markers during sarcolemmal differentiation in skeletal muscle cells

被引:23
作者
Draeger, A [1 ]
Monastyrskaya, K
Burkhard, FC
Wobus, AM
Moss, SE
Babiychuk, EB
机构
[1] Univ Bern, Inst Anat, Dept Cell Biol, CH-3012 Bern, Switzerland
[2] Univ Hosp Bern, Dept Urol, Bern, Switzerland
[3] Inst Plant Genet & Crop Plant Res, In Vitro Differentiat Grp, Gatersleben, Germany
[4] UCL, Inst Ophthalmol, Dept Cell Biol, London WC1E 6BT, England
[5] Kiev Taras Schevchenko Univ, Inst Physiol, Kiev, Ukraine
关键词
calcium; transverse tubular system; membrane microdomains; annexins; caveolin;
D O I
10.1016/S0012-1606(03)00398-1
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Muscle contraction implies flexibility in combination with force resistance and requires a high degree of sarcolemmal organization. Smooth muscle cells differentiate largely from mesenchymal precursor cells and gradually assume a highly periodic sarcolemmal organization. Skeletal muscle undergoes an even more striking differentiation programme, leading to cell fusion and alignment into myofibrils. The lipid bilayer of each cell type is further segregated into raft and non-raft microdomains of distinct lipid composition. Considering the extent of developmental rearrangement in skeletal muscle, we investigated sarcolemmal microdomain organization in skeletal and smooth muscle cells. The rafts in both muscle types are characterized by marker proteins belonging to the annexin family which localize to the inner membrane leaflet, as well as glycosyl-phosphatidyl-inositol (GPI)-anchored enzymes attached to the outer leaflet. We demonstrate that the profound structural rearrangements that occur during skeletal muscle maturation coincide with a striking decrease in membrane lipid segregation, downregulation of annexins 2 and 6, and a significant decrease in raft-associated 5'-nucleotidase activity. The relative paucity of lipid rafts in mature skeletal in contrast to smooth muscle suggests that the organization of sarcolemmal microdomains contributes to the muscle-specific differences in stimulatory responses and contractile properties. (C) 2003 Elsevier Inc. All rights reserved.
引用
收藏
页码:324 / 334
页数:11
相关论文
共 44 条
[1]   Cross-talk between caveolae and glycosylphosphatidylinositol-rich domains [J].
Abrami, L ;
Fivaz, M ;
Kobayashi, T ;
Kinoshita, T ;
Parton, RG ;
van der Goot, FG .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (33) :30729-30736
[2]   Annexin V, annexin VI, S100A1 and S100B in developing and adult avian skeletal muscles [J].
Arcuri, C ;
Giambanco, I ;
Bianchi, R ;
Donato, R .
NEUROSCIENCE, 2002, 109 (02) :371-388
[3]   Annexin VI participates in the formation of a reversible, membrane-cytoskeleton complex in smooth muscle cells [J].
Babiychuk, EB ;
Palstra, RJTS ;
Schaller, J ;
Kämpfer, U ;
Draeger, A .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (49) :35191-35195
[4]   Annexins in cell membrane dynamics:: Ca2+-regulated association of lipid microdomains [J].
Babiychuk, EB ;
Draeger, A .
JOURNAL OF CELL BIOLOGY, 2000, 150 (05) :1113-1123
[5]   Modulating signaling events in smooth muscle: cleavage of annexin 2 abolishes its binding to lipid rafts [J].
Babiychuk, EB ;
Monastyrskaya, K ;
Burkhard, FC ;
Wray, S ;
Draeger, A .
FASEB JOURNAL, 2002, 16 (10) :1177-1184
[6]   Annexin VI is attached to transverse-tubule membranes in isolated skeletal muscle triads [J].
Barrientos, G ;
Hidalgo, C .
JOURNAL OF MEMBRANE BIOLOGY, 2002, 188 (02) :163-173
[7]  
BLOCH RJ, 2002, CLIN ORTHOP S, V403, pS203, DOI DOI 10.1097/01.BLO.0000031982.92980.DA
[8]   Structure and function of sphingolipid- and cholesterol-rich membrane rafts [J].
Brown, DA ;
London, E .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (23) :17221-17224
[9]   Functions of lipid rafts in biological membranes [J].
Brown, DA ;
London, E .
ANNUAL REVIEW OF CELL AND DEVELOPMENTAL BIOLOGY, 1998, 14 :111-136
[10]   3 MUSCULAR-DYSTROPHIES - LOSS OF CYTOSKELETON EXTRACELLULAR-MATRIX LINKAGE [J].
CAMPBELL, KP .
CELL, 1995, 80 (05) :675-679