Differentiation and growth arrest signals are generated through the cytoplasmic region of gp130 that is essential for Stat3 activation

被引:200
作者
Yamanaka, Y [1 ]
Nakajima, K [1 ]
Fukada, T [1 ]
Hibi, M [1 ]
Hirano, T [1 ]
机构
[1] OSAKA UNIV, SCH MED, BIOMED RES CTR, DEPT MOLEC ONCOL, SUITA, OSAKA 565, JAPAN
关键词
differentiation; gp; 130; interleukin-6; M1; Stat; 3;
D O I
10.1002/j.1460-2075.1996.tb00500.x
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
Interleukin-6 (IL-6) induces growth arrest and macrophage differentiation through its receptor in a murine myeloid leukaemic cell line, M1, although it is largely unknown how the IL-6 receptor generates these signals. By using chimeric receptors consisting of the extracellular domain of growth hormone receptor and the transmembrane and cytoplasmic domain of gp130 with progressive C-terminal truncations, we showed that the membrane-proximal 133, but not 108, amino acids of gp130 could generate the signals for growth arrest, macrophage differentiation, down-regulation of c-myc and c-myb, induction of junB and IRF1 and Stat3 activation, Mutational analysis of this region showed that the tyrosine residue with the YXXQ motif was critical not only for Stat3 activation but also for growth arrest and differentiation, accompanied by down-regulation of c-myc and c-myb and immediate early induction of junB and IRF1. The tight correlation between Stat3 activation and other IL-6 functions was further observed in the context of the full-length cytoplasmic region of gp130. The results suggest that Stat3 plays an essential role in the signals for growth arrest and differentiation.
引用
收藏
页码:1557 / 1565
页数:9
相关论文
共 69 条
[51]   SIGNAL-TRANSDUCTION BY THE HIGH-AFFINITY GM-CSF RECEPTOR - 2 DISTINCT CYTOPLASMIC REGIONS OF THE COMMON BETA-SUBUNIT RESPONSIBLE FOR DIFFERENT SIGNALING [J].
SATO, N ;
SAKAMAKI, K ;
TERADA, N ;
ARAI, K ;
MIYAJIMA, A .
EMBO JOURNAL, 1993, 12 (11) :4181-4189
[52]   PROTEINS OF TRANSCRIPTION FACTOR ISGF-3 - ONE GENE ENCODES THE 91-KDA AND 84-KDA ISGF-3 PROTEINS THAT ARE ACTIVATED BY INTERFERON-ALPHA [J].
SCHINDLER, C ;
FU, XY ;
IMPROTA, T ;
AEBERSOLD, R ;
DARNELL, JE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (16) :7836-7839
[53]   Interferon-Dependent Tyrosine Phosphorylation of a Latent Cytoplasmic Transcription Factor (Reprinted from AAAS, vol 257, pg 809-813, 1992) [J].
Schindler, Chris ;
Shuai, Ke ;
Prezioso, Vincent R. ;
Darnell, James E., Jr. .
JOURNAL OF IMMUNOLOGY, 2011, 187 (11) :5489-5493
[54]   DEREGULATED C-MYB DISRUPTS INTERLEUKIN-6-INDUCED OR LEUKEMIA INHIBITORY FACTOR-INDUCED MYELOID DIFFERENTIATION PRIOR TO C-MYC - ROLE IN LEUKEMOGENESIS [J].
SELVAKUMARAN, M ;
LIEBERMANN, DA ;
HOFFMANLIEBERMANN, B .
MOLECULAR AND CELLULAR BIOLOGY, 1992, 12 (06) :2493-2500
[55]   THE NOVEL PRIMARY RESPONSE GENE MYD118 AND THE PROTOONCOGENES MYB, MYC, AND BCL-2 MODULATE TRANSFORMING GROWTH FACTOR-BETA-1-INDUCED APOPTOSIS OF MYELOID-LEUKEMIA CELLS [J].
SELVAKUMARAN, M ;
LIN, HK ;
SJIN, RTT ;
REED, JC ;
LIEBERMANN, DA ;
HOFFMAN, B .
MOLECULAR AND CELLULAR BIOLOGY, 1994, 14 (04) :2352-2360
[56]  
SHABO Y, 1988, BLOOD, V72, P2070
[57]   RAS-INDEPENDENT GROWTH-FACTOR SIGNALING BY TRANSCRIPTION FACTOR TYROSINE PHOSPHORYLATION [J].
SILVENNOINEN, O ;
SCHINDLER, C ;
SCHLESSINGER, J ;
LEVY, DE .
SCIENCE, 1993, 261 (5129) :1736-1739
[58]   ASSOCIATION AND ACTIVATION OF JAK-TYK KINASES BY CNTF-LIF-OSM-IL-6 BETA-RECEPTOR COMPONENTS [J].
STAHL, N ;
BOULTON, TG ;
FARRUGGELLA, T ;
IP, NY ;
DAVIS, S ;
WITTHUHN, BA ;
QUELLE, FW ;
SILVENNOINEN, O ;
BARBIERI, G ;
PELLEGRINI, S ;
IHLE, JN ;
YANCOPOULOS, GD .
SCIENCE, 1994, 263 (5143) :92-95
[59]   CHOICE OF STATS AND OTHER SUBSTRATES SPECIFIED BY MODULAR TYROSINE-BASED MOTIFS IN CYTOKINE RECEPTORS [J].
STAHL, N ;
FARRUGGELLA, TJ ;
BOULTON, TG ;
ZHONG, Z ;
DARNELL, JE ;
YANCOPOULOS, GD .
SCIENCE, 1995, 267 (5202) :1349-1353
[60]   INTERLEUKIN-6 TRIGGERS THE ASSOCIATION OF ITS RECEPTOR WITH A POSSIBLE SIGNAL TRANSDUCER, GP130 [J].
TAGA, T ;
HIBI, M ;
HIRATA, Y ;
YAMASAKI, K ;
YASUKAWA, K ;
MATSUDA, T ;
HIRANO, T ;
KISHIMOTO, T .
CELL, 1989, 58 (03) :573-581