Wnt5a Potentiates TGF-β Signaling to Promote Colonic Crypt Regeneration After Tissue Injury

Author:

Miyoshi Hiroyuki1,Ajima Rieko2,Luo Christine T.1,Yamaguchi Terry P.2,Stappenbeck Thaddeus S.1

Affiliation:

1. Department of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO 63110, USA.

2. Cancer and Developmental Biology Laboratory, Center for Cancer Research, National Cancer Institute-Frederick, NIH, Frederick, MD 21702, USA.

Abstract

Gut, Heal Thyself Foods, drugs, and pathogens all represent possible threats to our guts on a daily basis. Fortunately, the gut is quite good at repairing itself—but how? Working in mice, Miyoshi et al. (p. 108 , published online 6 September; see the Perspective by Barrett ) selectively injured intestinal crypts containing intestinal stem cells and observed therepair process. The noncanonical Wnt ligand, Wnt5a, was required for crypt regeneration. Wnt5a inhibited intestinal stem cell proliferation, which paradoxically promoted regeneration of crypt tissue.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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5. Crypt fission in the small intestine and colon. A mechanism for the emergence of G6PD locus-mutated crypts after treatment with mutagens;Park H. S.;Am. J. Pathol.,1995

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