RECEPTOR TYROSINE KINASE SPECIFIC FOR THE SKELETAL-MUSCLE LINEAGE - EXPRESSION IN EMBRYONIC MUSCLE, AT THE NEUROMUSCULAR-JUNCTION, AND AFTER INJURY

被引:361
作者
VALENZUELA, DM
STITT, TN
DISTEFANO, PS
ROJAS, E
MATTSSON, K
COMPTON, DL
NUNEZ, L
PARK, JS
STARK, JL
GIES, DR
THOMAS, S
LEBEAU, MM
FERNALD, AA
COPELAND, NG
JENKINS, NA
BURDEN, SJ
GLASS, DJ
YANCOPOULOS, GD
机构
[1] NYU, MED CTR, SKIRBALL INST, NEW YORK, NY 10016 USA
[2] UNIV CHICAGO, DEPT MED, HEMATOL ONCOL SECT, CHICAGO, IL 60637 USA
[3] NATL CANC INST, FREDERICK CANC RES CTR, ABL BASIC RES PROGRAM, MAMMALIAN GENET LAB, FREDERICK, MD 21703 USA
关键词
D O I
10.1016/0896-6273(95)90146-9
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
While a number of growth factors have been described that are highly specific for particular cell lineages, neither a factor nor a receptor uniquely specific to the skeletal muscle lineage has previously been described. Here we identify a receptor tyrosine kinase (RTK) specific to skeletal muscle, which we term ''MuSK'' for muscle-specific kinase. MuSK is expressed at low levels in proliferating myoblasts and is induced upon differentiation and fusion, In the embryo, it is specifically expressed in early myotomes and developing muscle. MUSK is then dramatically down-regulated in mature muscle, where it remains prominent only at the neuromuscular junction; MuSK is thus the only known RTK that localizes to the neuromuscular junction. Strikingly, MuSK expression is dramatically induced throughout the adult myofiber after denervation, block of electrical activity, or physical immobilization. In humans, MuSK maps to chromosome 9q31.3-32, which overlaps with the region reported to contain the Fukuyama muscular dystrophy mutation. Identification of MUSK introduces a novel receptor-factor system that seems sure to play an important and selective role in many aspects of skeletal muscle development and function.
引用
收藏
页码:573 / 584
页数:12
相关论文
共 41 条
  • [21] HISTOGENESIS OF RAT INTERCOSTAL MUSCLE
    KELLY, AM
    ZACKS, SI
    [J]. JOURNAL OF CELL BIOLOGY, 1969, 42 (01) : 135 - +
  • [22] AN EXTENDED FAMILY OF PROTEIN-TYROSINE KINASE GENES DIFFERENTIALLY EXPRESSED IN THE VERTEBRATE NERVOUS-SYSTEM
    LAI, C
    LEMKE, G
    [J]. NEURON, 1991, 6 (05) : 691 - 704
  • [23] THE INSULIN-RECEPTOR - STRUCTURE, FUNCTION, AND SIGNALING
    LEE, JS
    PILCH, PF
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY, 1994, 266 (02): : C319 - C334
  • [24] REGULATION OF MUSCLE-CELL GROWTH AND DIFFERENTIATION BY THE MYOD FAMILY OF HELIX-LOOP-HELIX PROTEINS
    LI, L
    OLSON, EN
    [J]. ADVANCES IN CANCER RESEARCH, 1992, 58 : 95 - 119
  • [25] MASIAKOWSKI P, 1992, J BIOL CHEM, V267, P26181
  • [26] MCMAHAN UJ, 1990, COLD SH Q B, V55, P407
  • [27] CYTOKINE RECEPTORS AND SIGNAL TRANSDUCTION
    MIYAJIMA, A
    KITAMURA, T
    HARADA, N
    YOKOTA, T
    ARAI, K
    [J]. ANNUAL REVIEW OF IMMUNOLOGY, 1992, 10 : 295 - 331
  • [28] INTERPLAY BETWEEN PROLIFERATION AND DIFFERENTIATION WITHIN THE MYOGENIC LINEAGE
    OLSON, EN
    [J]. DEVELOPMENTAL BIOLOGY, 1992, 154 (02) : 261 - 272
  • [29] THE ORGANOGENESIS OF MURINE STRIATED-MUSCLE - A CYTOARCHITECTURAL STUDY
    ONTELL, M
    KOZEKA, K
    [J]. AMERICAN JOURNAL OF ANATOMY, 1984, 171 (02): : 133 - 148
  • [30] MAPPING CHROMOSOME BAND 11Q23 IN HUMAN ACUTE-LEUKEMIA WITH BIOTINYLATED PROBES - IDENTIFICATION OF 11Q23 TRANSLOCATION BREAKPOINTS WITH A YEAST ARTIFICIAL CHROMOSOME
    ROWLEY, JD
    DIAZ, MO
    ESPINOSA, R
    PATEL, YD
    VANMELLE, E
    ZIEMIN, S
    TAILLONMILLER, P
    LICHTER, P
    EVANS, GA
    KERSEY, JH
    WARD, DC
    DOMER, PH
    LEBEAU, MM
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (23) : 9358 - 9362