Indian Hedgehog is an antagonist of Wnt signaling in colonic epithelial cell differentiation

被引:300
作者
van den Brink, GR
Bleuming, SA
Hardwick, JCH
Schepman, BL
Offerhaus, GJ
Keller, JJ
Nielsen, C
Gaffield, W
van Deventer, SJH
Roberts, DJ
Peppelenbosch, MP
机构
[1] Univ Amsterdam, Acad Med Ctr, Dept Expt Internal Med, NL-1105 AZ Amsterdam, Netherlands
[2] Univ Amsterdam, Acad Med Ctr, Dept Pathol, NL-1105 AZ Amsterdam, Netherlands
[3] Massachusetts Gen Hosp, Dept Pathol, Boston, MA 02114 USA
[4] ARS, Western Reg Res Ctr, USDA, Albany, CA USA
[5] Univ Amsterdam, Acad Med Ctr, Dept Gastroenterol, NL-1105 AZ Amsterdam, Netherlands
关键词
D O I
10.1038/ng1304
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Wnt signaling defines the colonic epithelial progenitor cell phenotype(1), and mutations in the gene adenomatous polyposis coli (APC) that activate the Wnt pathway cause the familial adenomatous polyposis coli (FAP) syndrome and most sporadic colon cancers(2). The mechanisms that regulate the transition of epithelial precursor cells into their differentiated derivatives are poorly characterized. We report that Indian hedgehog (Ihh) is expressed by mature colonocytes and regulates their differentiation in vitro and in vivo. Hedgehog (Hh) signaling restricts the expression of Wnt targets to the base of the colonic crypt in vivo, and transfection of Ihh into colon cancer cells leads to a downregulation of both components of the nuclear TCF4-beta-catenin complex and abrogates endogenous Wnt signaling in vitro. In turn, expression of Ihh is downregulated in polyps of individuals with FAP and expression of doxycycline-inducible dominant negative TCF4 (dnTCF4) restores Ihh expression in APC mutant DLD-1 colon cancer cells. These data identify a new Wnt-Hh axis in colonic epithelial renewal.
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收藏
页码:277 / 282
页数:6
相关论文
共 21 条
[1]   p21WAF1 is required for butyrate-mediated growth inhibition of human colon cancer cells [J].
Archer, SY ;
Meng, SF ;
Shei, A ;
Hodin, RA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (12) :6791-6796
[2]  
AUGERON C, 1984, CANCER RES, V44, P3961
[3]   Widespread requirement for Hedgehog ligand stimulation in growth of digestive tract tumours [J].
Berman, DM ;
Karhadkar, SS ;
Maitra, A ;
de Oca, RM ;
Gerstenblith, MR ;
Briggs, K ;
Parker, AR ;
Shimada, Y ;
Eshleman, JR ;
Watkins, DN ;
Beachy, PA .
NATURE, 2003, 425 (6960) :846-851
[4]   Linking colorectal cancer to Wnt signaling [J].
Bienz, M ;
Clevers, H .
CELL, 2000, 103 (02) :311-320
[5]   HEDGEHOG AND BMP GENES ARE COEXPRESSED AT MANY DIVERSE SITES OF CELL-CELL INTERACTION IN THE MOUSE EMBRYO [J].
BITGOOD, MJ ;
MCMAHON, AP .
DEVELOPMENTAL BIOLOGY, 1995, 172 (01) :126-138
[6]  
Boon EMJ, 2002, CANCER RES, V62, P5126
[7]   Inhibition of Hedgehog signaling by direct binding of cyclopamine to Smoothened [J].
Chen, JK ;
Taipale, J ;
Cooper, MK ;
Beachy, PA .
GENES & DEVELOPMENT, 2002, 16 (21) :2743-2748
[8]  
Hao XP, 2001, CANCER RES, V61, P8085
[9]   Bone morphogenetic protein 2 is expressed by, and acts upon, mature epithelial cells in the colon [J].
Hardwick, JCH ;
Van den Brink, GR ;
Bleuming, SA ;
Ballester, I ;
Van den Brande, JMH ;
Keller, JJ ;
Offerhaus, GJA ;
Van Deventer, SJH ;
Peppelenbosch, MP .
GASTROENTEROLOGY, 2004, 126 (01) :111-121
[10]   Constitutive transcriptional activation by a beta-catenin-Tcf complex in APC(-/-) colon carcinoma [J].
Korinek, V ;
Barker, N ;
Morin, PJ ;
vanWichen, D ;
deWeger, R ;
Kinzler, KW ;
Vogelstein, B ;
Clevers, H .
SCIENCE, 1997, 275 (5307) :1784-1787