Neuregulin isoforms exhibit distinct patterns of ErbB family receptor activation

被引:75
作者
Hobbs, SS
Coffing, SL
Le, AT
Cameron, EM
Williams, EE
Andrew, M
Blommel, EN
Hammer, RP
Chang, H
Riese, DJ
机构
[1] Purdue Univ, Dept Med Chem & Mol Pharmacol, W Lafayette, IN 47907 USA
[2] Louisiana State Univ, Dept Chem, Baton Rouge, LA 70803 USA
[3] Bristol Myers Squibb Co, Pharmaceut Res Inst, Princeton, NJ 08543 USA
关键词
heregulins; neuregulins; ErbB3; ErbB4; HER3; HER4;
D O I
10.1038/sj.onc.1205960
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
During the last decade, several novel members of the Epidermal Growth Factor family of peptide growth factors have been identified. Most prominent among these are the Neuregulins or Heregulins. To date, four different Neuregulin genes have been identified (Neuregulin1-4) and several different splicing isoforms have been identified for :at least two of these genes (Neuregulin1 and Neuregulin2). While Neuregulin1 isoforms have been extensively studied, comparatively little is known about Neuregulin3, Neuregulin4, or the Neuregulin2 isoforms. Indeed, there has been no systematic comparison of the activities of these molecules. Here we demonstrate that Neuregulin2alpha and Neuregulin2beta stimulate ErbB3 tyrosine phosphorylation and coupling to biological responses. In contrast, Neuregulin3 and Neuregulin4 fail to activate ErbB3 signaling. Furthermore, Neuregulin2beta, but not Neuregulin2alpha, stimulates ErbB4 tyrosine phosphorylation and coupling to biological responses. Finally, both Neuregulin3 and Neuregulin4 stimulate modest amounts of ErbB4 tyrosine phosphorylation. However, whereas Neuregulin3 stimulates a modest amount of ErbB4 coupling to biological responses, Neuregulin4 fails to stimulate ErbB4 coupling to biological responses. This suggests that there are qualitative as well as quantitative differences in ErbB family receptor activation by Neuregulin isoforms.
引用
收藏
页码:8442 / 8452
页数:11
相关论文
共 41 条
  • [1] Selection of heregulin variants having higher affinity for the ErbB3 receptor by monovalent phage display
    Ballinger, MD
    Jones, JT
    Lofgren, JA
    Fairbrother, WJ
    Akita, RW
    Sliwkowski, MX
    Wells, JA
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (19) : 11675 - 11684
  • [2] THE EPIDERMAL GROWTH-FACTOR
    BOONSTRA, J
    RIJKEN, P
    HUMBEL, B
    CREMERS, F
    VERKLEIJ, A
    HENEGOUWEN, PVE
    [J]. CELL BIOLOGY INTERNATIONAL, 1995, 19 (05) : 413 - 430
  • [3] Activation of neu (ErbB-2) mediated by disulfide bond-induced dimerization reveals a receptor tyrosine kinase dimer interface
    Burke, CL
    Stern, DF
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 1998, 18 (09) : 5371 - 5379
  • [4] Neuregulin-2, a new ligand of ErbB3/ErbB4-receptor tyrosine kinases
    Carraway, KL
    Weber, JL
    Unger, MJ
    Ledesma, J
    Yu, N
    Gassmann, M
    Lai, C
    [J]. NATURE, 1997, 387 (6632) : 512 - 516
  • [5] Ligands for ErbB-family receptors encoded by a neuregulin-like gene
    Chang, H
    Riese, DJ
    Gilbert, W
    Stern, DF
    McMahan, UJ
    [J]. NATURE, 1997, 387 (6632) : 509 - 512
  • [6] Virocrine transformation
    DrummondBarbosa, D
    DiMaio, D
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA-REVIEWS ON CANCER, 1997, 1332 (01): : M1 - M17
  • [7] ErbB2 and ErbB3 do not quantitatively modulate ligand-induced ErbB4 tyrosine phosphorylation
    Feroz, K
    Williams, E
    Riese, DJ
    [J]. CELLULAR SIGNALLING, 2002, 14 (09) : 793 - 798
  • [8] STRUCTURE-FUNCTION-RELATIONSHIPS FOR THE EGF/TGF-ALPHA FAMILY OF MITOGENS
    GROENEN, LC
    NICE, EC
    BURGESS, AW
    [J]. GROWTH FACTORS, 1994, 11 (04) : 235 - 257
  • [9] The Type 1 growth factor receptors and their ligands considered as a complex system
    Gullick, WJ
    [J]. ENDOCRINE-RELATED CANCER, 2001, 8 (02) : 75 - 82
  • [10] Neuregulin-4: a novel growth factor that acts through the ErbB-4 receptor tyrosine kinase
    Harari, D
    Tzahar, E
    Romano, J
    Shelly, M
    Pierce, JH
    Andrews, GC
    Yarden, Y
    [J]. ONCOGENE, 1999, 18 (17) : 2681 - 2689