c/EBPβ Is a Major Regulatory Element Driving Transcriptional Activation of the CXCL12 Promoter

被引:22
作者
Calonge, E. [1 ]
Alonso-Lobo, J. M. [1 ]
Escandon, C. [1 ]
Gonzalez, N. [1 ]
Bermejo, M. [1 ]
Santiago, B. [2 ]
Mestre, L. [3 ]
Pablos, J. L. [2 ]
Caruz, A. [4 ]
Alcami, J. [1 ]
机构
[1] Inst Salud Carlos III, Ctr Nacl Microbiol, AIDS Immunopathol Unit, Madrid 28220, Spain
[2] Hosp 12 Octubre, Unidad Invest, E-28041 Madrid, Spain
[3] CSIC, Inst Cajal, E-28002 Madrid, Spain
[4] Univ Jaen, Dept Biol Expt, Immunogenet Grp, Jaen, Spain
关键词
CXCL12; chemokine; promoter regulation; c/EBP beta transcription factor; CELL-DERIVED FACTOR-1; FACTOR-I; GLIOBLASTOMA CELLS; TUMOR-GROWTH; EXPRESSION; GENE; RECEPTOR; INDUCTION; SDF-1; MICROENVIRONMENT;
D O I
10.1016/j.jmb.2009.11.064
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
CXCL12 is considered a constitutively expressed chemokine with homeo-static functions. However, induction of CXCL12 expression and its potential role in several pathologic conditions have been reported, suggesting that CXCL12 gene expression can be induced by different stimuli. To elucidate the molecular mechanisms involved in the regulation of CXCL12 gene expression, we aim to define the molecular factors that operate at the transcriptional level. Basal, constitutive expression of CXCL12 was dependent on basic helix-loop-helix factors. Transcriptional up-regulation of the CXCL12 gene was induced by cellular confluence or inflammatory stimuli such as interleukin-1 and interleukin-6, in a CCAAT/enhancer binding protein beta (c/EBP beta)-dependent manner. Chromatin immunoprecipitation assays confirmed c/EBP beta binding to a specific response element located at -1171 of the promoter region of CXCL12. Our data show that c/EBP beta is a major regulatory element driving transcription of the CXCL12 gene in response to cytokines and cell confluence. (C) 2009 Published by Elsevier Ltd.
引用
收藏
页码:463 / 472
页数:10
相关论文
共 44 条
[1]   The Effects of Hypoxia/Reoxygenation on the Physiological Behaviour of U373-Mg Astrocytes [J].
Aldinucci, Carlo ;
Maiorca, Silvia Maria ;
De Rosa, Paola ;
Palmi, Mitri ;
Sticozzi, Claudia ;
Ciccoli, Lucia ;
Leoncini, Silvia ;
Signorini, Cinzia ;
Pessina, Gian Paolo .
NEUROCHEMICAL RESEARCH, 2010, 35 (01) :42-49
[2]   SDF-1 synergistically enhances IL-3-induced activation of the Raf-1/MEK/Erk signaling pathway through activation of Rac and its effector Pak kinases to promote hematopoiesis and chemotaxis [J].
Arai, A ;
Jin, A ;
Yan, WH ;
Mizuchi, D ;
Yamamoto, K ;
Nanki, T ;
Miura, O .
CELLULAR SIGNALLING, 2005, 17 (04) :497-506
[3]   A natural classification of the basic helix-loop-helix class of transcription factors [J].
Atchley, WR ;
Fitch, WM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (10) :5172-5176
[4]   Human chemokines: An update [J].
Baggiolini, M ;
Dewald, B ;
Moser, B .
ANNUAL REVIEW OF IMMUNOLOGY, 1997, 15 :675-705
[5]   A highly efficacious lymphocyte chemoattractant, stromal cell-derived factor 1 (SDF-1) [J].
Bleul, CC ;
Fuhlbrigge, RC ;
Casasnovas, JM ;
Aiuti, A ;
Springer, TA .
JOURNAL OF EXPERIMENTAL MEDICINE, 1996, 184 (03) :1101-1109
[6]   CXCR4: a key receptor in the crosstalk between tumor cells and their microenvironment [J].
Burger, JA ;
Kipps, TJ .
BLOOD, 2006, 107 (05) :1761-1767
[7]   Homing to hypoxia: HIF-1 as a mediator of progenitor cell recruitment to injured tissue [J].
Ceradini, DJ ;
Gurtner, GC .
TRENDS IN CARDIOVASCULAR MEDICINE, 2005, 15 (02) :57-63
[8]   Stromal cell-derived factor-1 promotes bone marrow-derived cells differentiation to cardiomyocyte phenotypes in vitro [J].
Chen, M. ;
Xie, H. -Q. ;
Deng, L. ;
Li, X. -Q. ;
Wang, Y. ;
Zhi, W. ;
Yang, Z. -M. .
CELL PROLIFERATION, 2008, 41 (02) :336-347
[9]   Role of the CCAAT/enhancer binding protein-α transcription factor in the glucocorticoid stimulation of p21waf1/cip1 gene promoter activity in growth-arrested rat hepatoma cells [J].
Cram, EJ ;
Ramos, RA ;
Wang, EC ;
Cha, HH ;
Nishio, Y ;
Firestone, GL .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (04) :2008-2014
[10]   CXCR4 expression mediates glioma cell invasiveness [J].
Ehtesham, M ;
Winston, JA ;
Kabos, P ;
Thompson, RC .
ONCOGENE, 2006, 25 (19) :2801-2806