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:83
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.
引用
收藏
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 [J].
Kim, HK ;
Hawley, TS ;
Hawley, RG ;
Baumann, H .
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 [J].
LAI, CF ;
RIPPERGER, J ;
MORELLA, KK ;
WANG, YP ;
GEARING, DP ;
FEY, GH ;
BAUMANN, H .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (25) :14847-14850
[33]   CILIARY NEUROTROPHIC FACTOR ENHANCES THE SURVIVAL OF PURKINJE-CELLS IN-VITRO [J].
LARKFORS, L ;
LINDSAY, RM ;
ALDERSON, RF .
EUROPEAN JOURNAL OF NEUROSCIENCE, 1994, 6 (06) :1015-1025
[34]   PURIFICATION, CLONING, AND EXPRESSION OF CILIARY NEUROTROPHIC FACTOR (CNTF) [J].
LIN, LFH ;
MISMER, D ;
LILE, JD ;
ARMES, LG ;
BUTLER, ET ;
VANNICE, JL ;
COLLINS, F .
SCIENCE, 1989, 246 (4933) :1023-1025
[35]   ASSOCIATION OF TRANSCRIPTION FACTOR APRF AND PROTEIN-KINASE JAK1 WITH THE INTERLEUKIN-6 SIGNAL TRANSDUCER GP130 [J].
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 .
SCIENCE, 1994, 263 (5143) :89-92
[36]   DISRUPTION OF THE CNTF GENE RESULTS IN MOTOR-NEURON DEGENERATION [J].
MASU, Y ;
WOLF, E ;
HOLTMANN, B ;
SENDTNER, M ;
BREM, G ;
THOENEN, H .
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 [J].
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 .
CELL, 1996, 84 (03) :431-442
[38]   ARREST OF MOTOR-NEURON DISEASE IN WOBBLER MICE COTREATED WITH CNTF AND BDNF [J].
MITSUMOTO, H ;
IKEDA, K ;
KLINKOSZ, B ;
CEDARBAUM, JM ;
WONG, V ;
LINDSAY, RM .
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 [J].
Miyakawa, Y ;
Rojnuckarin, P ;
Habib, T ;
Kaushansky, K .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (04) :2494-2502
[40]   IL-6-INDUCED HOMODIMERIZATION OF GP-130 AND ASSOCIATED ACTIVATION OF A TYROSINE KINASE [J].
MURAKAMI, M ;
HIBI, M ;
NAKAGAWA, N ;
NAKAGAWA, T ;
YASUKAWA, K ;
YAMANISHI, K ;
TAGA, T ;
KISHIMOTO, T .
SCIENCE, 1993, 260 (5115) :1808-1810