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.
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页码:22476 / 22484
页数:9
相关论文
共 74 条
[1]   Suckling defect in mice lacking the soluble haemopoietin receptor NR6 [J].
Alexander, WS ;
Rakar, S ;
Robb, L ;
Farley, A ;
Willson, TA ;
Zhang, JG ;
Hartley, L ;
Kikuchi, Y ;
Kojima, T ;
Nomura, H ;
Hasegawa, M ;
Maeda, M ;
Fabri, L ;
Jachno, K ;
Nash, A ;
Metcalf, D ;
Nicola, NA ;
Hilton, DJ .
CURRENT BIOLOGY, 1999, 9 (11) :605-608
[2]  
BAUMANN H, 1993, J BIOL CHEM, V268, P8414
[3]   NEUROPOIETIC CYTOKINES IN THE HEMATOPOIETIC FOLD [J].
BAZAN, JF .
NEURON, 1991, 7 (02) :197-208
[4]   Regulation of gliogenesis in the central nervous system by the JAK-STAT signaling pathway [J].
Bonni, A ;
Sun, Y ;
NadalVicens, M ;
Bhatt, A ;
Frank, DA ;
Rozovsky, I ;
Stahl, N ;
Yancopoulos, GD ;
Greenberg, ME .
SCIENCE, 1997, 278 (5337) :477-483
[5]   CHARACTERIZATION OF A PATHWAY FOR CILIARY NEUROTROPHIC FACTOR SIGNALING TO THE NUCLEUS [J].
BONNI, A ;
FRANK, DA ;
SCHINDLER, C ;
GREENBERG, ME .
SCIENCE, 1993, 262 (5139) :1575-1579
[6]  
BOULTON TG, 1994, J BIOL CHEM, V269, P11648
[7]   STAT3 ACTIVATION BY CYTOKINES UTILIZING GP130 AND RELATED TRANSDUCERS INVOLVES A SECONDARY MODIFICATION REQUIRING AN H7-SENSITIVE KINASE [J].
BOULTON, TG ;
ZHONG, Z ;
WEN, ZL ;
DARNELL, JE ;
STAHL, N ;
YANCOPOULOS, GD .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (15) :6915-6919
[8]   Receptor recognition by gp130 cytokines [J].
Bravo, J ;
Heath, JK .
EMBO JOURNAL, 2000, 19 (11) :2399-2411
[9]   Functional interaction of STAT3 transcription factor with the cell cycle inhibitor p21WAF1/CIP1/SD11 [J].
Coqueret, O ;
Gascan, H .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (25) :18794-18800
[10]   LIFR-BETA AND GP-130 AS HETERODIMERIZING SIGNAL TRANSDUCERS OF THE TRIPARTITE CNTF RECEPTOR [J].
DAVIS, S ;
ALDRICH, TH ;
STAHL, N ;
PAN, L ;
TAGA, T ;
KISHIMOTO, T ;
IP, NY ;
YANCOPOULOS, GD .
SCIENCE, 1993, 260 (5115) :1805-1808