Signaling pathways recruited by the cardiotrophin-like cytokine/cytokine-like factor-1 composite cytokine -: Specific requirement of the membrane-bound form of ciliary neurotrophic factor receptor α component

被引:82
作者
Lelièvre, E
Plun-Favreau, H
Chevalier, S
Froger, J
Guillet, C
Elson, GCA
Gauchat, JF
Gascan, H
机构
[1] CHU Angers, INSERM EMI 9928, F-49003 Angers, France
[2] Ctr Immunol Pierre Fabre, F-74164 St Julien En Genevois, France
关键词
D O I
10.1074/jbc.M101681200
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
Ciliary neurotrophic factor (CNTF) is a cytokine sup porting the differentiation and survival of a number of neural cell types. Its receptor complex consists of a ligand-binding component, CNTF receptor (CNTFR), associated with two signaling receptor components, gp130 and leukemia inhibitory factor receptor (LIFR), Striking phenotypic differences between CNTF- and CNTFR-deficient mice suggest that CNTFR serves as a receptor for a second developmentally important ligand, We recently demonstrated that cardiotrophin-like cytokine (CLC) associates with the soluble orphan receptor cytokine-like factor-1 (CLF) to form a heterodimeric cytokine that displayed activities only on cells expressing the tripartite CNTF receptor on their surface. In this present study we examined the membrane binding of the CLC/CLF composite cytokine and observed a preferential interaction of the cytokine with the CNTFR subunit. Signaling pathways recruited by the CLC/CLF complex in human neuroblastoma cell lines were also analyzed in detail. The results obtained showed an activation of Janus kinases (JAK1, JAK2, and TYK2) leading to a tyrosine phosphorylation of the gp130 and LIFR, The phosphorylated signaling receptors served in turn as docking proteins for signal transducing molecules such as STAT3 and SHP-2, In vitro analysis revealed that the gp130-LIFR pathway could also stimulate the phosphatidylinositol 3-kinase and the mitogen-activated protein kinase pathways. In contrast to that reported before for CNTF, soluble CNTFR failed to promote the action CLC/CLF, and an absolute requirement of the membrane form of CNTFR was required to generate a functional response to the composite cytokine. This study reinforces the functional similarity between CNTF and the CLC/CLF composite cytokine defining the second ligand for CNTFR.
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页码:22476 / 22484
页数:9
相关论文
共 74 条
  • [31] Protein tyrosine phosphatase 2 (SHP-2) moderates signaling by gp130 but is not required for the induction of acute-phase plasma protein genes in hepatic cells
    Kim, HK
    Hawley, TS
    Hawley, RG
    Baumann, H
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 1998, 18 (03) : 1525 - 1533
  • [32] SEPARATE SIGNALING MECHANISMS ARE INVOLVED IN THE CONTROL OF STAT PROTEIN-ACTIVATION AND GENE-REGULATION VIA THE INTERLEUKIN-6 RESPONSE ELEMENT BY THE BOX-3 MOTIF OF GP130
    LAI, CF
    RIPPERGER, J
    MORELLA, KK
    WANG, YP
    GEARING, DP
    FEY, GH
    BAUMANN, H
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (25) : 14847 - 14850
  • [33] CILIARY NEUROTROPHIC FACTOR ENHANCES THE SURVIVAL OF PURKINJE-CELLS IN-VITRO
    LARKFORS, L
    LINDSAY, RM
    ALDERSON, RF
    [J]. EUROPEAN JOURNAL OF NEUROSCIENCE, 1994, 6 (06) : 1015 - 1025
  • [34] PURIFICATION, CLONING, AND EXPRESSION OF CILIARY NEUROTROPHIC FACTOR (CNTF)
    LIN, LFH
    MISMER, D
    LILE, JD
    ARMES, LG
    BUTLER, ET
    VANNICE, JL
    COLLINS, F
    [J]. SCIENCE, 1989, 246 (4933) : 1023 - 1025
  • [35] ASSOCIATION OF TRANSCRIPTION FACTOR APRF AND PROTEIN-KINASE JAK1 WITH THE INTERLEUKIN-6 SIGNAL TRANSDUCER GP130
    LUTTICKEN, C
    WEGENKA, UM
    YUAN, JP
    BUSCHMANN, J
    SCHINDLER, C
    ZIEMIECKI, A
    HARPUR, AG
    WILKS, AF
    YASUKAWA, K
    TAGA, T
    KISHIMOTO, T
    BARBIERI, G
    PELLEGRINI, S
    SENDTNER, M
    HEINRICH, PC
    HORN, F
    [J]. SCIENCE, 1994, 263 (5143) : 89 - 92
  • [36] DISRUPTION OF THE CNTF GENE RESULTS IN MOTOR-NEURON DEGENERATION
    MASU, Y
    WOLF, E
    HOLTMANN, B
    SENDTNER, M
    BREM, G
    THOENEN, H
    [J]. NATURE, 1993, 365 (6441) : 27 - 32
  • [37] Targeted disruption of the STAT1 gene in mice reveals unexpected physiologic specificity in the JAK-STAT signaling pathway
    Meraz, MA
    White, JM
    Sheehan, KCF
    Bach, EA
    Rodig, SJ
    Dighe, AS
    Kaplan, DH
    Riley, JK
    Greenlund, AC
    Campbell, D
    CarverMoore, K
    DuBois, RN
    Clark, R
    Aguet, M
    Schreiber, RD
    [J]. CELL, 1996, 84 (03) : 431 - 442
  • [38] ARREST OF MOTOR-NEURON DISEASE IN WOBBLER MICE COTREATED WITH CNTF AND BDNF
    MITSUMOTO, H
    IKEDA, K
    KLINKOSZ, B
    CEDARBAUM, JM
    WONG, V
    LINDSAY, RM
    [J]. SCIENCE, 1994, 265 (5175) : 1107 - 1110
  • [39] Thrombopoietin induces phosphoinositol 3-kinase activation through SHP2, Gab, and insulin receptor substrate proteins in BAF3 cells and primary murine megakaryocytes
    Miyakawa, Y
    Rojnuckarin, P
    Habib, T
    Kaushansky, K
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (04) : 2494 - 2502
  • [40] IL-6-INDUCED HOMODIMERIZATION OF GP-130 AND ASSOCIATED ACTIVATION OF A TYROSINE KINASE
    MURAKAMI, M
    HIBI, M
    NAKAGAWA, N
    NAKAGAWA, T
    YASUKAWA, K
    YAMANISHI, K
    TAGA, T
    KISHIMOTO, T
    [J]. SCIENCE, 1993, 260 (5115) : 1808 - 1810