ErbB4 and its isoforms -: Selective regulation of growth factor responses by naturally occurring receptor variants

被引:114
作者
Junttila, TT
Sundvall, M
Määttä, JA
Elenius, K
机构
[1] Univ Turku, Med Res Labs, FIN-20520 Turku, Finland
[2] Univ Turku, Dept Med Biochem & Mol Biol, FIN-20520 Turku, Finland
基金
芬兰科学院;
关键词
D O I
10.1016/S1050-1738(01)00065-2
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
ErbB4 is a member of the epidermal growth factor receptor (EGFR, ErbB) family that mediates responses to neuregulins and other EGF-like growth factors. ErbB4 is a central regulator of cardiovascular and neural development as well as differentiation of the mammary gland. A role for ErbB4 has also been implicated in malignancies and heart diseases. Four structurally and functionally distinct ErbB4 isoforms have recently been identified. One pair of isoforms differs within their extracellular juxtamembrane domains. These juxtamembrane ErbB4 isoforms are either susceptible or resistant to proteolytic processing that release a soluble receptor ectodomain. Another pair of ErbB4 isoforms differs within their cytoplasmic tails. Analysis of the intracellular signal transduction pathways indicates that both cytoplasmic ErbB4 isoforms can couple to the Shc-MAPK signaling pathway, while the other one is incapable of coupling to the phosphoinositide 3-kinase (PI3-K)-Akt pathway. The differences in the activation of signaling cascades are reflected in the cellular responses stimulated via the cytoplasmic isoforms. Both cytoplasmic ErbB4 isoforms can stimulate proliferation, but the isoform that cannot activate PI3-K is defective in stimulating cellular survival and chemotaxis. Together these four naturally occurring receptor variants provide a new level of diversity to the control of growth factor-stimulated cellular responses. Thus, the ErbB4 isoforms may have distinct and specific roles in the regulation of various developmental and pathological processes. (Trends Cardiovasc Med 10;2000:304-310). (C) 2001, Elsevier Science Inc.
引用
收藏
页码:304 / 310
页数:7
相关论文
共 63 条
[1]   The ErbB signaling network in embryogenesis and oncogenesis: Signal diversification through combinatorial ligand-receptor interactions [J].
Alroy, I ;
Yarden, Y .
FEBS LETTERS, 1997, 410 (01) :83-86
[2]   Vascular endothelial growth factor up-regulation via p21-activated kinase-1 signaling regulates heregulin-β1-mediated angiogenesis [J].
Bagheri-Yarmand, R ;
Vadlamudi, RK ;
Wang, RA ;
Mendelsohn, J ;
Kumar, R .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (50) :39451-39457
[3]  
Baulida J, 1996, J BIOL CHEM, V271, P5251
[4]   Neuregulins and their receptors: A versatile signaling module in organogenesis and oncogenesis [J].
Burden, S ;
Yarden, Y .
NEURON, 1997, 18 (06) :847-855
[5]   Multinational study of the efficacy and safety of humanized anti-HER2 monoclonal antibody in women who have HER2-overexpressing metastatic breast cancer that has progressed after chemotherapy for metastatic disease [J].
Cobleigh, MA ;
Vogel, CL ;
Tripathy, D ;
Robert, NJ ;
Scholl, S ;
Fehrenbacher, L ;
Wolter, JM ;
Paton, V ;
Shak, S ;
Lieberman, G ;
Slamon, DJ .
JOURNAL OF CLINICAL ONCOLOGY, 1999, 17 (09) :2639-2648
[6]   The relationship between human epidermal growth-like factor receptor expression and cellular transformation in NIH3T3 cells [J].
Cohen, BD ;
Kiener, PA ;
Green, JM ;
Foy, L ;
Fell, HP ;
Zhang, K .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (48) :30897-30903
[7]   The HER-2/neu receptor tyrosine kinase gene encodes a secreted autoinhibitor [J].
Doherty, JK ;
Bond, C ;
Jardim, A ;
Adelman, JP ;
Clinton, GM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (19) :10869-10874
[8]   LIGAND AND PROTEIN KINASE-C DOWNMODULATE THE COLONY-STIMULATING FACTOR-I RECEPTOR BY INDEPENDENT MECHANISMS [J].
DOWNING, JR ;
ROUSSEL, MF ;
SHERR, CJ .
MOLECULAR AND CELLULAR BIOLOGY, 1989, 9 (07) :2890-2896
[9]   HETERODIMERIZATION AND FUNCTIONAL INTERACTION BETWEEN EGF RECEPTOR FAMILY MEMBERS - A NEW SIGNALING PARADIGM WITH IMPLICATIONS FOR BREAST-CANCER RESEARCH [J].
EARP, HS ;
DAWSON, TL ;
LI, X ;
YU, H .
BREAST CANCER RESEARCH AND TREATMENT, 1995, 35 (01) :115-132
[10]   Activation of HER4 by heparin-binding EGF-like growth factor stimulates chemotaxis but not proliferation [J].
Elenius, K ;
Paul, S ;
Allison, G ;
Sun, J ;
Klagsbrun, M .
EMBO JOURNAL, 1997, 16 (06) :1268-1278