BMP signaling inhibits intestinal stem cell self-renewal through suppression of Wnt-beta-catenin signaling - PubMed (original) (raw)
. 2004 Oct;36(10):1117-21.
doi: 10.1038/ng1430. Epub 2004 Sep 19.
Jiwang Zhang, Wei-Gang Tong, Ossama Tawfik, Jason Ross, David H Scoville, Qiang Tian, Xin Zeng, Xi He, Leanne M Wiedemann, Yuji Mishina, Linheng Li
Affiliations
- PMID: 15378062
- DOI: 10.1038/ng1430
BMP signaling inhibits intestinal stem cell self-renewal through suppression of Wnt-beta-catenin signaling
Xi C He et al. Nat Genet. 2004 Oct.
Abstract
In humans, mutations in BMPR1A, SMAD4 and PTEN are responsible for juvenile polyposis syndrome, juvenile intestinal polyposis and Cowden disease, respectively. The development of polyposis is a common feature of these diseases, suggesting that there is an association between BMP and PTEN pathways. The mechanistic link between BMP and PTEN pathways and the related etiology of juvenile polyposis is unresolved. Here we show that conditional inactivation of Bmpr1a in mice disturbs homeostasis of intestinal epithelial regeneration with an expansion of the stem and progenitor cell populations, eventually leading to intestinal polyposis resembling human juvenile polyposis syndrome. We show that BMP signaling suppresses Wnt signaling to ensure a balanced control of stem cell self-renewal. Mechanistically, PTEN, through phosphatidylinosital-3 kinase-Akt, mediates the convergence of the BMP and Wnt pathways on control of beta-catenin. Thus, BMP signaling may control the duplication of intestinal stem cells, thereby preventing crypt fission and the subsequent increase in crypt number.
Comment in
- Linking pathways in colorectal cancer.
van den Brink GR. van den Brink GR. Nat Genet. 2004 Oct;36(10):1038-9. doi: 10.1038/ng1004-1038. Nat Genet. 2004. PMID: 15454939 No abstract available. - Re-examination of P-PTEN staining patterns in the intestinal crypt.
Bjerknes M, Cheng H. Bjerknes M, et al. Nat Genet. 2005 Oct;37(10):1016-7; author reply 1017-8. doi: 10.1038/ng1005-1016. Nat Genet. 2005. PMID: 16195712 No abstract available.
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