The sarcomeric Z-disc: a nodal point in signalling and disease

被引:180
作者
Frank, Derk
Kuhn, Christian
Katus, Hugo A.
Frey, Norbert
机构
[1] Heidelberg Univ, Dept Cardiol, D-69120 Heidelberg, Germany
[2] Heidelberg Univ, Dept Internal Med 3, D-69120 Heidelberg, Germany
来源
JOURNAL OF MOLECULAR MEDICINE-JMM | 2006年 / 84卷 / 06期
关键词
striated muscle; Sarcomere; Z-disc; heart; skeletal muscle; myopathy; cardiomyopathy; stretch receptor; muscle dystrophy; cell biology;
D O I
10.1007/s00109-005-0033-1
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The perception of the Z-disc in striated muscle has undergone significant changes in the past decade. Traditionally, the Z-disc has been viewed as a passive constituent of the sarcomere, which is important only for the cross-linking of thin filaments and transmission of force generated by the myofilaments. The recent discovery of multiple novel molecular components, however, has shed light on an emerging role for the Z-disc in signal transduction in both cardiac and skeletal muscles. Strikingly, mutations in several Z-disc proteins have been shown to cause cardiomyopathies and/or muscular dystrophies. In addition, the elusive cardiac stretch receptor appears to localize to the Z-disc. Various signalling molecules have been shown to interact with Z-disc proteins, several of which shuttle between the Z-disc and other cellular compartments such as the nucleus, underlining the dynamic nature of Z-disc-dependent signalling. In this review, we provide a systematic view on the currently known Z-disc components and the functional significance of the Z-disc as an interface between biomechanical sensing and signalling in cardiac and skeletal muscle functions and diseases.
引用
收藏
页码:446 / 468
页数:23
相关论文
共 288 条
[131]  
Lane P. W., 1985, MOUSE NEWS LETT, V73, P18
[132]   The kinase domain of titin controls muscle gene expression and protein turnover [J].
Lange, S ;
Xiang, FQ ;
Yakovenko, A ;
Vihola, A ;
Hackman, P ;
Rostkova, E ;
Kristensen, J ;
Brandmeier, B ;
Franzen, G ;
Hedberg, B ;
Gunnarsson, LG ;
Hughes, SM ;
Marchand, S ;
Sejersen, T ;
Richard, I ;
Edström, L ;
Ehler, E ;
Udd, B ;
Gautel, M .
SCIENCE, 2005, 308 (5728) :1599-1603
[133]   Subcellular targeting of metabolic enzymes to titin in heart muscle may be mediated by DRAL/FHL-2 [J].
Lange, S ;
Auerbach, D ;
McLoughlin, P ;
Perriard, E ;
Schäfer, BW ;
Perriard, JC ;
Ehler, E .
JOURNAL OF CELL SCIENCE, 2002, 115 (24) :4925-4936
[134]   CELL TYPE-SPECIFIC ASSOCIATION BETWEEN 2 TYPES OF SPECTRIN AND 2 TYPES OF INTERMEDIATE FILAMENTS [J].
LANGLEY, RC ;
COHEN, CM .
CELL MOTILITY AND THE CYTOSKELETON, 1987, 8 (02) :165-173
[135]   Integrin activation and focal complex formation in cardiac hypertrophy [J].
Laser, M ;
Willey, CD ;
Jiang, WJ ;
Cooper, G ;
Menick, DR ;
Zile, MR ;
Kuppuswamy, D .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (45) :35624-35630
[136]   IMMUNOLOGICAL CHARACTERIZATION OF SUBUNIT OF 100 A FILAMENTS FROM MUSCLE-CELLS [J].
LAZARIDES, E ;
HUBBARD, BD .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1976, 73 (12) :4344-4348
[137]   Regulation of muscle mass by myostatin [J].
Lee, SJ .
ANNUAL REVIEW OF CELL AND DEVELOPMENTAL BIOLOGY, 2004, 20 :61-86
[138]   Desmin mutation responsible for idiopathic dilated cardiomyopathy [J].
Li, DX ;
Tapscoft, T ;
Gonzalez, O ;
Burch, PE ;
Quiñones, MA ;
Zoghbi, WA ;
Hill, R ;
Bachinski, LL ;
Mann, DL ;
Roberts, R .
CIRCULATION, 1999, 100 (05) :461-464
[139]   Atrogin-1/rnuscle atrophy F-box inhibits calcineurin-dependent cardiac hypertrophy by participating in an SCF ubiquitin ligase complex [J].
Li, HH ;
Kedar, V ;
Zhang, CL ;
McDonough, H ;
Arya, R ;
Wang, DZ ;
Patterson, C .
JOURNAL OF CLINICAL INVESTIGATION, 2004, 114 (08) :1058-1071
[140]   Desmin is essential for the tensile strength and integrity of myofibrils but not for myogenic commitment, differentiation, and fusion of skeletal muscle [J].
Li, ZL ;
Mericskay, M ;
Agbulut, O ;
ButlerBrowne, G ;
Carlsson, L ;
Thornell, LE ;
Babinet, C ;
Paulin, D .
JOURNAL OF CELL BIOLOGY, 1997, 139 (01) :129-144