Neuregulins: functions, forms, and signaling strategies

被引:841
作者
Falls, DL [1 ]
机构
[1] Emory Univ, Dept Neurol, Ctr Neurodegenerat Disorders, Rm 2105,1510 Clifton Rd, Atlanta, GA 30322 USA
关键词
neuregulin; acetylcholine receptor-inducing activity; glial growth factor; heregulin; neu differentiation factor; sensory and motor neuron-derived factor; ErbB receptor tyrosine kinase; schizophrenia; neuromuscular synapse; cell-cell signaling proteins; juxtacrine signaling; paracrine signaling; transmembrane ligands; proteolytic process; shredding;
D O I
10.1016/S0014-4827(02)00102-7
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The neuregulins (NRGs) are cell-cell signaling proteins that are ligands for receptor tyrosine kinases of the ErbB family. The neuregulin family of genes has four members: NRG1, NRG2, NRG3, and NRG4. Relatively little is known about the biological functions of the NRG2, 3, and 4 proteins, and they are considered in this review only briefly. The NRG1 proteins play essential roles in the nervous system, heart, and breast. There is also evidence for involvement of NRG signaling in the development and function of several other organ systems, and in human disease, including the pathogenesis of schizophrenia and breast cancer. There are many NRG1 isoforms, raising the question "Why so many neuregulins?" Study of mice with targeted mutations ("knockout mice") has demonstrated that isoforms differing in their N-terminal region or in their epidermal growth factor (EGF)-like domain differ in their in vivo functions. These differences in function might arise because of differences in expression pattern or might reflect differences in intrinsic biological characteristics. While differences in expression pattern certainly contribute to the observed differences in in vivo functions, there are also marked differences in intrinsic characteristics that may tailor isoforms for specific signaling requirements, a theme that will be emphasized in this review. (C) 2003 Elsevier Science (USA). All rights reserved.
引用
收藏
页码:14 / 30
页数:17
相关论文
共 187 条
  • [1] Adlkofer K, 2000, GLIA, V29, P104, DOI 10.1002/(SICI)1098-1136(20000115)29:2<104::AID-GLIA2>3.0.CO
  • [2] 2-2
  • [3] ALIMANDI M, 1995, ONCOGENE, V10, P1813
  • [4] Anton ES, 1997, DEVELOPMENT, V124, P3501
  • [5] AVILA MA, 1995, ONCOGENE, V10, P963
  • [6] Vascular endothelial growth factor up-regulation via p21-activated kinase-1 signaling regulates heregulin-β1-mediated angiogenesis
    Bagheri-Yarmand, R
    Vadlamudi, RK
    Wang, RA
    Mendelsohn, J
    Kumar, R
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (50) : 39451 - 39457
  • [7] BAO J, 1999, SOC NEUR ABSTR, V25
  • [8] Axonal control of oligodendrocyte development
    Barres, BA
    Raff, MC
    [J]. JOURNAL OF CELL BIOLOGY, 1999, 147 (06) : 1123 - 1128
  • [9] Neuregulin expression in PNS neurons: isoforms and regulation by target interactions
    Bermingham-McDonogh, O
    Xu, YT
    Marchionni, MA
    Scherer, SS
    [J]. MOLECULAR AND CELLULAR NEUROSCIENCE, 1997, 10 (3-4) : 184 - 195
  • [10] ADAMs: focus on the protease domain
    Black, RA
    White, JM
    [J]. CURRENT OPINION IN CELL BIOLOGY, 1998, 10 (05) : 654 - 659