Cdx1 promotes differentiation in a rat intestinal epithelial cell line
- PMID: 10579974
- DOI: 10.1016/s0016-5085(99)70283-0
Cdx1 promotes differentiation in a rat intestinal epithelial cell line
Abstract
Background & aims: Homeobox genes are involved in establishing and maintaining differentiated patterns in adult tissues. Cdx1 might carry out that function in the intestinal epithelium because its expression is specific to that tissue and increases during development.
Methods: Cdx1 expression was induced in IEC-6 intestinal epithelial cells by stable transfection, and subsequent changes in cell growth, resistance to apoptosis, migration, and differentiation were monitored.
Results: Compared with control, IEC-6/Cdx1 cells proliferated more rapidly, were more resistant to apoptosis, and migrated 3-4 times faster, as shown by an in vitro wound assay. IEC-6/Cdx1 cells in culture formed multilayers. Morphology of the top layer was similar to that of columnar epithelium, with cells showing typical features of differentiated enterocytes, including complex junctions and well-developed microvilli with glycocalix. Expression of 2 markers of enterocyte differentiation, aminopeptidase N and villin, was induced in IEC-6/Cdx1 cells. Aminopeptidase N was targeted to the basolateral membrane, and villin was localized to the cytoplasm. Actin filaments, which were mostly present in transcytoplasmic stress fibers in control cells, were redistributed to the cortex in Cdx1-transfected cells.
Conclusions: Cdx1 expression in IEC-6 cells induces phenotypic changes characteristic of differentiating enterocytes, suggesting an important role for Cdx1 in the transition from stem cells to proliferating/transit cells.
Similar articles
-
Cdx1 promotes cellular growth of epithelial intestinal cells through induction of the secretory protein PAP I.Eur J Cell Biol. 2001 Feb;80(2):156-63. doi: 10.1078/0171-9335-00148. Eur J Cell Biol. 2001. PMID: 11302520
-
Differentiated intestinal epithelial cells exhibit increased migration through polyamines and myosin II.Am J Physiol. 1999 Dec;277(6):G1149-58. doi: 10.1152/ajpgi.1999.277.6.G1149. Am J Physiol. 1999. PMID: 10600811
-
Homeobox gene Cdx1 regulates Ras, Rho and PI3 kinase pathways leading to transformation and tumorigenesis of intestinal epithelial cells.Oncogene. 2001 Jul 12;20(31):4180-7. doi: 10.1038/sj.onc.1204551. Oncogene. 2001. PMID: 11464284
-
The murine Cdx1 gene product localises to the proliferative compartment in the developing and regenerating intestinal epithelium.Differentiation. 1998 Nov;64(1):11-8. doi: 10.1046/j.1432-0436.1998.6410011.x. Differentiation. 1998. PMID: 9921649
-
Activation of K(+) channels and increased migration of differentiated intestinal epithelial cells after wounding.Am J Physiol Cell Physiol. 2002 Apr;282(4):C885-98. doi: 10.1152/ajpcell.00361.2001. Am J Physiol Cell Physiol. 2002. PMID: 11880277
Cited by
-
Computational Identification of Key Regulators in Two Different Colorectal Cancer Cell Lines.Front Genet. 2016 Apr 5;7:42. doi: 10.3389/fgene.2016.00042. eCollection 2016. Front Genet. 2016. PMID: 27092172 Free PMC article.
-
Beta-catenin--a linchpin in colorectal carcinogenesis?Am J Pathol. 2002 Feb;160(2):389-401. doi: 10.1016/s0002-9440(10)64856-0. Am J Pathol. 2002. PMID: 11839557 Free PMC article. Review.
-
Down-regulation of a gastric transcription factor, Sox2, and ectopic expression of intestinal homeobox genes, Cdx1 and Cdx2: inverse correlation during progression from gastric/intestinal-mixed to complete intestinal metaplasia.J Cancer Res Clin Oncol. 2004 Mar;130(3):135-45. doi: 10.1007/s00432-003-0519-6. Epub 2003 Dec 4. J Cancer Res Clin Oncol. 2004. PMID: 14655050 Free PMC article.
-
The epigenetic signature of CFTR expression is co-ordinated via chromatin acetylation through a complex intronic element.Biochem J. 2007 Dec 15;408(3):317-26. doi: 10.1042/BJ20070282. Biochem J. 2007. PMID: 17848139 Free PMC article.
-
The multi-omic landscape of transcription factor inactivation in cancer.Genome Med. 2016 Aug 25;8(1):89. doi: 10.1186/s13073-016-0342-8. Genome Med. 2016. PMID: 27562343 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Research Materials