THE LIF RESPONSE ELEMENT OF THE ALPHA(2) MACROGLOBULIN GENE CONFERS LIF-INDUCED TRANSCRIPTIONAL ACTIVATION IN EMBRYONAL STEM-CELLS

被引:24
作者
HOCKE, GM
CUI, MZ
FEY, GH
机构
[1] Institute for Microbiology, Biochemistry and Genetics, University of Erlangen, Nürnberg
关键词
CYTOKINE RECEPTORS; EMBRYONAL STEM CELLS; INTERLEUKIN 6-TYPE CYTOKINES; LEUKEMIA INHIBITORY FACTOR; STAT FACTORS;
D O I
10.1006/cyto.1995.0067
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
Leukaemia Inhibitory Factor (LIF), an interleukin 6 (IL-6)-type cytokine, is an essential growth factor for murine embryonal stem cells, The LIE-receptor was known in these cells, but the cell-internal part of the signal cascade and the transcription factors through which LIF controls its growth-promoting target genes in embryonal stem cells, had not been identified, This study shows that the type LI IL-6-response element of the rat alpha(2) macroglobulin (alpha(2)M) gene, which mediates IL-6- and LIE-responses in hepatic cells, also functioned as a LIE-response element (LIE-RE) in ES1 embryonal stem cells and P19 embryonal carcinoma cells, It conferred transcriptional activation by LIF of transfected reporter constructs in these cells, A characteristic DNA-binding activity interacting with this LIE-RE was induced by treatment of these cells with LIE The complex between this activity and the LIF-RE had identical electrophoretic mobility, sequence-specificity and kinetics of induction as the complex with the corresponding LIE-response factor (LIF-RF) from hepatic cells, The transcription factor STAT3 was part of this complex, as shown by its reactivity with anti-STAT3 antibodies, Withdrawal of LIF from ES1 cells caused the induction of differentiation and the disappearance of this DNA-binding activity, Simultaneously, the surface density of high-affinity LIF receptors was reduced approximately 10-fold. (C) 1995 Academic Press Limited.
引用
收藏
页码:491 / 502
页数:12
相关论文
共 53 条
[1]   MOLECULAR-CLONING OF APRF, A NOVEL IFN-STIMULATED GENE FACTOR-3 P91-RELATED TRANSCRIPTION FACTOR INVOLVED IN THE GP130-MEDIATED SIGNALING PATHWAY [J].
AKIRA, S ;
NISHIO, Y ;
INOUE, M ;
WANG, XJ ;
WEI, S ;
MATSUSAKA, T ;
YOSHIDA, K ;
SUDO, T ;
NARUTO, M ;
KISHIMOTO, T .
CELL, 1994, 77 (01) :63-71
[2]  
AUSUBEL FM, 1990, CURRENT PROTOCOLS MO
[3]  
BAFFET G, 1991, MOL BIOL MED, V8, P141
[4]  
BAUMANN H, 1989, J BIOL CHEM, V264, P8046
[5]  
BAUMANN H, 1989, J IMMUNOL, V143, P1163
[6]  
BRECHNER T, 1991, MOL BIOL MED, V8, P267
[7]   THE MAJOR LAMININ RECEPTOR OF MOUSE EMBRYONIC STEM-CELLS IS A NOVEL ISOFORM OF THE ALPHA-6-BETA-1 INTEGRIN [J].
COOPER, HM ;
TAMURA, RN ;
QUARANTA, V .
JOURNAL OF CELL BIOLOGY, 1991, 115 (03) :843-850
[8]   JAK-STAT PATHWAYS AND TRANSCRIPTIONAL ACTIVATION IN RESPONSE TO IFNS AND OTHER EXTRACELLULAR SIGNALING PROTEINS [J].
DARNELL, JE ;
KERR, IM ;
STARK, GR .
SCIENCE, 1994, 264 (5164) :1415-1421
[9]   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
[10]   FIREFLY LUCIFERASE GENE - STRUCTURE AND EXPRESSION IN MAMMALIAN-CELLS [J].
DEWET, JR ;
WOOD, KV ;
DELUCA, M ;
HELINSKI, DR ;
SUBRAMANI, S .
MOLECULAR AND CELLULAR BIOLOGY, 1987, 7 (02) :725-737