Functional receptor for GDNF encoded by the c-ret proto-oncogene

被引:691
|
作者
Trupp, M
Arenas, E
Fainzilber, M
Nilsson, AS
Sieber, BA
Grigoriou, M
Kilkenny, C
SalazarGrueso, E
Pachnis, V
Arumae, U
Sariola, H
Saarma, M
Ibanez, CF
机构
[1] KAROLINSKA INST,DEPT MED BIOCHEM & BIOPHYS,MOLEC NEUROBIOL LAB,S-17177 STOCKHOLM,SWEDEN
[2] NATL INST MED RES,DIV DEV NEUROBIOL,LONDON NW7 1AA,ENGLAND
[3] UNIV CHICAGO,BRAIN RES INST,DEPT NEUROL,CHICAGO,IL 60637
[4] UNIV HELSINKI,INST BIOTECHNOL,PROGRAM MOL NEUROBIOL,FIN-00014 HELSINKI,FINLAND
[5] UNIV HELSINKI,INST BIOTECHNOL,PROGRAM DEV BIOL,FIN-00014 HELSINKI,FINLAND
关键词
D O I
10.1038/381785a0
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
GLIAL-CELL-LINE-DERIVED neurotrophic factor (GDNF) promotes the survival and phenotype of central dopaminergic(1,2), noradrenergic(3) and motor neurons(4-6), as well as various subpopulations of peripheral sensory and sympathetic neurons(7,8). GDNF is structurally related to members of the transforming growth factor (TGF)-beta superfamily(9), several members of which have well-characterized receptor systems(10,11); however, GDNF receptors still remain undefined. Here we show that GDNF binds to, and induces tyrosine phosphorylation of, the product of the c-ret proto-oncogene, an orphan receptor tyrosine kinase, in a GDNF-responsive motor-neuron cell line. Ret protein could also bind GDNF and mediate survival and growth responses to GDNF upon transfection into naive fibroblasts. Moreover, high levels of c-ret mRNA expression were found in dopaminergic neurons of the adult substantia nigra, where exogenous GDNF protected Ret-positive neurons from 6-hydroxydopamine-induced cell death, Thus the product of the c-ret proto-oncogene encodes a functional receptor for GDNF that may mediate its neurotrophic effects on motor and dopaminergic neurons.
引用
收藏
页码:785 / 789
页数:5
相关论文
共 50 条
  • [1] Developmental and denervation changes in c-ret proto-oncogene expression in chick motoneurons
    Nakamura, M
    Ohta, K
    Hirokawa, K
    Fukushima, M
    Uchino, M
    Ando, M
    Tanaka, H
    MOLECULAR BRAIN RESEARCH, 1996, 39 (1-2): : 1 - 11
  • [2] Expression of RET proto-oncogene and GDNF deficit in Hirschsprung's disease
    Zhan, JH
    Xiu, Y
    Gu, JQ
    Fang, ZC
    Hu, XL
    JOURNAL OF PEDIATRIC SURGERY, 1999, 34 (11) : 1606 - 1609
  • [3] Establishing high resolution melting analysis: method validation and evaluation for c-RET proto-oncogene mutation screening
    Benej, Martin
    Bendlova, Bela
    Vaclavikova, Eliska
    Poturnajova, Martina
    CLINICAL CHEMISTRY AND LABORATORY MEDICINE, 2012, 50 (01) : 51 - 60
  • [4] RET proto-oncogene and thyroid cancer
    Komminoth, P
    ENDOCRINE PATHOLOGY, 1997, 8 (03) : 235 - 239
  • [5] RET proto-oncogene and thyroid cancer
    Paul Komminoth
    Endocrine Pathology, 1997, 8 : 235 - 239
  • [6] The RET proto-oncogene in sporadic pheochromocytomas
    Takaya, K
    Yoshimasa, T
    Arai, H
    Tamura, N
    Miyamoto, Y
    Itoh, H
    Nakao, K
    INTERNAL MEDICINE, 1996, 35 (06) : 449 - 452
  • [7] The RET proto-oncogene in human cancers
    Jhiang, SM
    ONCOGENE, 2000, 19 (49) : 5590 - 5597
  • [8] The RET proto-oncogene in human cancers
    Sissy M Jhiang
    Oncogene, 2000, 19 : 5590 - 5597
  • [9] Idiopathic slow-transit constipation is not associated with mutations of the RET proto-oncogene or GDNF
    Knowles, CH
    Gayther, SA
    Scott, M
    Ramus, S
    Anand, P
    Williams, NS
    Ponder, BA
    DISEASES OF THE COLON & RECTUM, 2000, 43 (06) : 851 - 857
  • [10] Complementary and overlapping expression of glial cell line-derived neurotrophic factor (GDNF), c-ret proto-oncogene, and GDNF receptor-alpha indicates multiple mechanisms of trophic actions in the adult rat CNS
    Trupp, M
    Belluardo, N
    Funakoshi, H
    Ibanez, CF
    JOURNAL OF NEUROSCIENCE, 1997, 17 (10): : 3554 - 3567