Striated muscle cytoarchitecture: An intricate web of form and function

被引:429
作者
Clark, KA [1 ]
McElhinny, AS
Beckerle, MC
Gregorio, CC
机构
[1] Univ Utah, Huntsman Canc Inst, Salt Lake City, UT 84112 USA
[2] Univ Utah, Dept Biol, Salt Lake City, UT 84112 USA
[3] Univ Arizona, Dept Cell Biol & Anat, Tucson, AZ 85724 USA
[4] Univ Arizona, Dept Mol & Cellular Biol, Tucson, AZ 85724 USA
关键词
sarcomere; cytoskeleton; Z-line; thick filament; thin filament;
D O I
10.1146/annurev.cellbio.18.012502.105840
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Striated muscle is an intricate, efficient, and precise machine that contains complex interconnected cytoskeletal networks critical for its contractile activity. The individual units of the sarcomere, the basic contractile unit of myofibrils, include the thin, thick, titin, and nebulin filaments. These filament systems have been investigated intensely for some time, but the details of their functions, as well as how they are connected to other cytoskeletal elements, are just beginning to be elucidated. These investigations have advanced significantly in recent years through the identification of novel sarcomeric and sarcomeric-associated proteins and their subsequent functional analyses in model systems. Mutations in these cytoskeletal components account for a large percentage of human myopathies, and thus insight into the normal functions of these proteins has provided a much needed mechanistic understanding of these disorders. In this review, we highlight the components of striated muscle cytoarchitecture with respect to their interactions, dynamics, links to signaling pathways, and functions. The exciting conclusion is that the striated muscle cytoskeleton, an exquisitely tuned, dynamic molecular machine, is capable of responding to subtle changes in cellular physiology.
引用
收藏
页码:637 / 706
页数:74
相关论文
共 473 条
[1]   Myoadenylate deaminase deficiency with progressive muscle weakness and atrophy caused by new missense mutations in AMPD1 gene: case report in a Japanese patient [J].
Abe, M ;
Higuchi, I ;
Morisaki, H ;
Morisaki, T ;
Osame, M .
NEUROMUSCULAR DISORDERS, 2000, 10 (07) :472-477
[2]   Growth and muscle defects in mice lacking adult myosin heavy chain genes [J].
AcakpoSatchivi, LJR ;
Edelmann, W ;
Sartorius, C ;
Lu, BD ;
Wahr, PA ;
Watkins, SC ;
Metzger, JM ;
Leinwand, L ;
Kucherlapati, R .
JOURNAL OF CELL BIOLOGY, 1997, 139 (05) :1219-1229
[3]  
ADAMS JC, 1993, DEVELOPMENT, V117, P1183
[4]   A novel marker for vertebrate embryonic heart, the EH-myomesin isoform [J].
Agarkova, I ;
Auerbach, D ;
Ehler, E ;
Perriard, JC .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (14) :10256-10264
[5]   Cardiac ankyrin repeat protein is a novel marker of cardiac hypertrophy - Role of M-CAT element within the promoter [J].
Aihara, Y ;
Kurabayashi, M ;
Saito, Y ;
Ohyama, Y ;
Tanaka, T ;
Takeda, S ;
Tomaru, K ;
Sekiguchi, K ;
Arai, M ;
Nakamura, T ;
Nagai, R .
HYPERTENSION, 2000, 36 (01) :48-53
[6]   Different pathways regulate expression of the skeletal myosin heavy chain genes [J].
Allen, DL ;
Sartorius, CA ;
Sycuro, LK ;
Leinwand, LA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (47) :43524-43533
[7]   Identification of a novel tropomodulin isoform, skeletal tropomodulin, that caps actin filament pointed ends in fast skeletal muscle [J].
Almenar-Queralt, A ;
Lee, A ;
Conley, CA ;
de Pouplana, LR ;
Fowler, VM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (40) :28466-28475
[8]   Skeletal muscle-specific myosin binding protein-H is expressed in Purkinje fibers of the cardiac conduction system [J].
Alyonycheva, T ;
CohenGould, L ;
Siewert, C ;
Fischman, DA ;
Mikawa, T .
CIRCULATION RESEARCH, 1997, 80 (05) :665-672
[9]  
AMPE C, 1999, GUIDEBOOK CYTOSKELET, P11
[10]   A common variant of the AMPD1 gene predicts improved cardiovascular survival in patients with coronary artery disease [J].
Anderson, JL ;
Habashi, J ;
Carlquist, JF ;
Muhlestein, JB ;
Horne, BD ;
Bair, TL ;
Pearson, RR .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2000, 36 (04) :1248-1252