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
[41]   IDENTIFICATION OF A NOVEL INTERLEUKIN-6 RESPONSE ELEMENT CONTAINING AN ETS-BINDING SITE AND A CRE-LIKE SITE IN THE JUNB PROMOTER [J].
NAKAJIMA, K ;
KUSAFUKA, T ;
TAKEDA, T ;
FUJITANI, Y ;
NAKAE, K ;
HIRANO, T .
MOLECULAR AND CELLULAR BIOLOGY, 1993, 13 (05) :3027-3041
[42]   THE ZINC FINGER TRANSCRIPTION FACTOR EGR-1 IS ESSENTIAL FOR AND RESTRICTS DIFFERENTIATION ALONG THE MACROPHAGE LINEAGE [J].
NGUYEN, HQ ;
HOFFMANLIEBERMANN, B ;
LIEBERMANN, DA .
CELL, 1993, 72 (02) :197-209
[43]   A MACROPHAGE-DERIVED FACTOR REQUIRED BY PLASMACYTOMAS FOR SURVIVAL AND PROLIFERATION INVITRO [J].
NORDAN, RP ;
POTTER, M .
SCIENCE, 1986, 233 (4763) :566-569
[44]  
ORITANI K, 1992, BLOOD, V80, P2298
[45]   P53-INDEPENDENT EXPRESSION OF P21(CIP)1 IN MUSCLE AND OTHER TERMINALLY DIFFERENTIATING CELLS [J].
PARKER, SB ;
EICHELE, G ;
ZHANG, PM ;
RAWLS, A ;
SANDS, AT ;
BRADLEY, A ;
OLSON, EN ;
HARPER, JW ;
ELLEDGE, SJ .
SCIENCE, 1995, 267 (5200) :1024-1027
[46]   CARDIOTROPHIN-1 - BIOLOGICAL-ACTIVITIES AND BINDING TO THE LEUKEMIA INHIBITORY FACTOR-RECEPTOR GP130 SIGNALING COMPLEX [J].
PENNICA, D ;
SHAW, KJ ;
SWANSON, TA ;
MOORE, MW ;
SHELTON, DL ;
ZIONCHECK, KA ;
ROSENTHAL, A ;
TAGA, T ;
PAONI, NF ;
WOOD, WI .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (18) :10915-10922
[47]   INDUCTION BY EGF AND INTERFERON-GAMMA OF TYROSINE-PHOSPHORYLATED DNA-BINDING PROTEINS IN MOUSE-LIVER NUCLEI [J].
RUFFJAMISON, S ;
CHEN, K ;
COHEN, S .
SCIENCE, 1993, 261 (5129) :1733-1736
[48]   A COMMON NUCLEAR SIGNAL-TRANSDUCTION PATHWAY ACTIVATED BY GROWTH-FACTOR AND CYTOKINE RECEPTORS [J].
SADOWSKI, HB ;
SHUAI, K ;
DARNELL, JE ;
GILMAN, MZ .
SCIENCE, 1993, 261 (5129) :1739-1744
[49]   CRITICAL CYTOPLASMIC DOMAINS OF THE COMMON BETA-SUBUNIT OF THE HUMAN GM-CSF, IL-3 AND IL-5 RECEPTORS FOR GROWTH SIGNAL TRANSDUCTION AND TYROSINE PHOSPHORYLATION [J].
SAKAMAKI, K ;
MIYAJIMA, I ;
KITAMURA, T ;
MIYAJIMA, A .
EMBO JOURNAL, 1992, 11 (10) :3541-3549
[50]  
Sambrook J., 1989, MOL CLONING LAB MANU