File Download
Links for fulltext
(May Require Subscription)
- Publisher Website: 10.1053/j.gastro.2010.06.014
- Scopus: eid_2-s2.0-77956168783
- PMID: 20542037
- WOS: WOS:000281365500031
- Find via
Supplementary
- Citations:
- Appears in Collections:
Article: Indian hedgehog regulates intestinal stem cell fate through epithelial-mesenchymal interactions during development
Title | Indian hedgehog regulates intestinal stem cell fate through epithelial-mesenchymal interactions during development | ||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Authors | |||||||||||||
Keywords | BMP ECM Hedgehog Signaling MMP | ||||||||||||
Issue Date | 2010 | ||||||||||||
Publisher | WB Saunders Co. The Journal's web site is located at http://www.elsevier.com/locate/gastro | ||||||||||||
Citation | Gastroenterology, 2010, v. 139 n. 3, p. 893-903 How to Cite? | ||||||||||||
Abstract | Background & Aims Intestinal stem cells (ISCs) are regulated by the mesenchymal environment via physical interaction and diffusible factors. We examined the role of Indian hedgehog (Ihh) in mesenchymal organization and the mechanisms by which perturbations in epithelial-mesenchymal interactions affect ISC fate. Methods We generated mice with intestinal epithelial-specific disruption of Ihh. Gross and microscopic anatomical changes were determined using histologic, immunohistochemical, and in situ hybridization analyses. Molecular mechanisms were elucidated by expression profiling and in vitro analyses. Results Deletion of intestinal epithelial Ihh disrupted the intestinal mesenchymal architecture, demonstrated by loss of the muscularis mucosae, deterioration of the extracellular matrix, and reductions in numbers of crypt myofibroblasts. Concurrently, the epithelial compartment had increased Wnt signaling, disturbed crypt polarity and architecture, defective enterocyte differentiation, and increased and ectopic proliferation that was accompanied by increased numbers of ISCs. Mechanistic studies revealed that Hh inhibition deregulates bone morphogenetic protein signaling, increases matrix metalloproteinase levels, and disrupts extracellular matrix proteins, fostering a proliferative environment for ISCs and progenitor cells. Conclusions Ihh regulates ISC self-renewal and differentiation. Intestinal epithelial Ihh signals to the mesenchymal compartment to regulate formation and proliferation of mesenchymal cells, which in turn affect epithelial proliferation and differentiation. These findings provide a basis for analyses of the role of the muscularis mucosae in ISC regulation. © 2010 by the AGA Institute. | ||||||||||||
Persistent Identifier | http://hdl.handle.net/10722/123825 | ||||||||||||
ISSN | 2023 Impact Factor: 25.7 2023 SCImago Journal Rankings: 7.362 | ||||||||||||
PubMed Central ID | |||||||||||||
ISI Accession Number ID |
Funding Information: This work is supported in part by National Institutes of Health grants R21DK069309 and R01CA136606 to X.C.; R01CA127229 and R01DK55783 to D.W.P.; a grant from the Research Grants Council of the Hong Kong Special Administrative Region (Project No. HKU7524/06M) to S.Y.L. and X.C.; a grant from Strategic Research Theme on Cancer from The University of Hong Kong to S.Y.L. C.K. is supported by a stem cell fellowship provided by the California Institute for Regenerative Medicine; and D.E.S. is supported by Deutsche Forschungsgemeinschaft (DFG, Sta1065/1-1). The funding agencies have no role in data collection, analysis, and interpretation. | ||||||||||||
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Kosinski, C | en_HK |
dc.contributor.author | Stange, DE | en_HK |
dc.contributor.author | Xu, C | en_HK |
dc.contributor.author | Chan, AS | en_HK |
dc.contributor.author | Ho, C | en_HK |
dc.contributor.author | Yuen, ST | en_HK |
dc.contributor.author | Mifflin, RC | en_HK |
dc.contributor.author | Powell, DW | en_HK |
dc.contributor.author | Clevers, H | en_HK |
dc.contributor.author | Leung, SY | en_HK |
dc.contributor.author | Chen, X | en_HK |
dc.date.accessioned | 2010-09-29T03:56:55Z | - |
dc.date.available | 2010-09-29T03:56:55Z | - |
dc.date.issued | 2010 | en_HK |
dc.identifier.citation | Gastroenterology, 2010, v. 139 n. 3, p. 893-903 | en_HK |
dc.identifier.issn | 0016-5085 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/123825 | - |
dc.description.abstract | Background & Aims Intestinal stem cells (ISCs) are regulated by the mesenchymal environment via physical interaction and diffusible factors. We examined the role of Indian hedgehog (Ihh) in mesenchymal organization and the mechanisms by which perturbations in epithelial-mesenchymal interactions affect ISC fate. Methods We generated mice with intestinal epithelial-specific disruption of Ihh. Gross and microscopic anatomical changes were determined using histologic, immunohistochemical, and in situ hybridization analyses. Molecular mechanisms were elucidated by expression profiling and in vitro analyses. Results Deletion of intestinal epithelial Ihh disrupted the intestinal mesenchymal architecture, demonstrated by loss of the muscularis mucosae, deterioration of the extracellular matrix, and reductions in numbers of crypt myofibroblasts. Concurrently, the epithelial compartment had increased Wnt signaling, disturbed crypt polarity and architecture, defective enterocyte differentiation, and increased and ectopic proliferation that was accompanied by increased numbers of ISCs. Mechanistic studies revealed that Hh inhibition deregulates bone morphogenetic protein signaling, increases matrix metalloproteinase levels, and disrupts extracellular matrix proteins, fostering a proliferative environment for ISCs and progenitor cells. Conclusions Ihh regulates ISC self-renewal and differentiation. Intestinal epithelial Ihh signals to the mesenchymal compartment to regulate formation and proliferation of mesenchymal cells, which in turn affect epithelial proliferation and differentiation. These findings provide a basis for analyses of the role of the muscularis mucosae in ISC regulation. © 2010 by the AGA Institute. | en_HK |
dc.language | eng | - |
dc.publisher | WB Saunders Co. The Journal's web site is located at http://www.elsevier.com/locate/gastro | en_HK |
dc.relation.ispartof | Gastroenterology | en_HK |
dc.rights | This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. | - |
dc.subject | BMP | en_HK |
dc.subject | ECM | en_HK |
dc.subject | Hedgehog Signaling | en_HK |
dc.subject | MMP | en_HK |
dc.subject.mesh | Cell Communication | - |
dc.subject.mesh | Colon - metabolism - pathology | - |
dc.subject.mesh | Epithelial Cells - metabolism - pathology | - |
dc.subject.mesh | Hedgehog Proteins - deficiency - genetics - metabolism | - |
dc.subject.mesh | Intestinal Mucosa - metabolism - pathology | - |
dc.title | Indian hedgehog regulates intestinal stem cell fate through epithelial-mesenchymal interactions during development | en_HK |
dc.type | Article | en_HK |
dc.identifier.openurl | http://library.hku.hk:4550/resserv?sid=HKU:IR&issn=0016-5085&volume=139&issue=3&spage=893&epage=903&date=2010&atitle=Indian+hedgehog+regulates+intestinal+stem+cell+fate+through+epithelial-mesenchymal+interactions+during+development | - |
dc.identifier.email | Leung, SY:suetyi@hkucc.hku.hk | en_HK |
dc.identifier.authority | Leung, SY=rp00359 | en_HK |
dc.description.nature | postprint | - |
dc.identifier.doi | 10.1053/j.gastro.2010.06.014 | en_HK |
dc.identifier.pmid | 20542037 | - |
dc.identifier.pmcid | PMC2930094 | - |
dc.identifier.scopus | eid_2-s2.0-77956168783 | en_HK |
dc.identifier.hkuros | 174354 | - |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-77956168783&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 139 | en_HK |
dc.identifier.issue | 3 | en_HK |
dc.identifier.spage | 893 | en_HK |
dc.identifier.epage | 903 | en_HK |
dc.identifier.isi | WOS:000281365500031 | - |
dc.publisher.place | United States | en_HK |
dc.identifier.issnl | 0016-5085 | - |