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Cdx function is required for maintenance of intestinal identity in the adult

The homeodomain transcription factors Cdx1 and Cdx2 are expressed in the intestinal epithelium from early development, with expression persisting throughout the life of the animal. While our understanding of the function of Cdx members in intestinal development has advanced significantly, their role...

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Bibliographic Details
Published in:Developmental biology 2012-03, Vol.363 (2), p.426-437
Main Authors: Hryniuk, Alexa, Grainger, Stephanie, Savory, Joanne G.A., Lohnes, David
Format: Article
Language:English
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Summary:The homeodomain transcription factors Cdx1 and Cdx2 are expressed in the intestinal epithelium from early development, with expression persisting throughout the life of the animal. While our understanding of the function of Cdx members in intestinal development has advanced significantly, their roles in the adult intestine is relatively poorly understood. In the present study, we found that ablation of Cdx2 in the adult small intestine severely impacted villus morphology, proliferation and intestinal gene expression patterns, resulting in the demise of the animal. Long-term loss of Cdx2 in a chimeric model resulted in loss of all differentiated intestinal cell types and partial conversion of the mucosa to a gastric-like epithelium. Concomitant loss of Cdx1 did not exacerbate any of these phenotypes. Loss of Cdx2 in the colon was associated with a shift to a cecum-like epithelial morphology and gain of cecum-associated genes which was more pronounced with subsequent loss of Cdx1. These findings suggest that Cdx2 is essential for differentiation of the small intestinal epithelium, and that both Cdx1 and Cdx2 contribute to homeostasis of the colon. ► Cdx2 is critical for differentiation of all cell types of the adult small intestine ► In the absence of Cdx2, Cdx1 cannot support homeostasis of the small intestine ► The finding of a role for Cdx1 with Cdx2 in patterning of the colon epithelium
ISSN:0012-1606
1095-564X
DOI:10.1016/j.ydbio.2012.01.010