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Canonical Wnt signals combined with suppressed TGFβ/BMP pathways promote renewal of the native human colonic epithelium.
Gut. 2014 Apr; 63(4):610-21.Gut

Abstract

BACKGROUND

A defining characteristic of the human intestinal epithelium is that it is the most rapidly renewing tissue in the body. However, the processes underlying tissue renewal and the mechanisms that govern their coordination have proved difficult to study in the human gut.

OBJECTIVE

To investigate the regulation of stem cell-driven tissue renewal by canonical Wnt and TGFβ/bone morphogenetic protein (BMP) pathways in the native human colonic epithelium.

DESIGN

Intact human colonic crypts were isolated from mucosal tissue samples and placed into 3D culture conditions optimised for steady-state tissue renewal. High affinity mRNA in situ hybridisation and immunohistochemistry were complemented by functional genomic and bioimaging techniques. The effects of signalling pathway modulators on the status of intestinal stem cell biology, crypt cell proliferation, migration, differentiation and shedding were determined.

RESULTS

Native human colonic crypts exhibited distinct activation profiles for canonical Wnt, TGFβ and BMP pathways. A population of intestinal LGR5/OLFM4-positive stem/progenitor cells were interspersed between goblet-like cells within the crypt-base. Exogenous and crypt cell-autonomous canonical Wnt signals supported homeostatic intestinal stem/progenitor cell proliferation and were antagonised by TGFβ or BMP pathway activation. Reduced Wnt stimulation impeded crypt cell proliferation, but crypt cell migration and shedding from the crypt surface were unaffected and resulted in diminished crypts.

CONCLUSIONS

Steady-state tissue renewal in the native human colonic epithelium is dependent on canonical Wnt signals combined with suppressed TGFβ/BMP pathways. Stem/progenitor cell proliferation is uncoupled from crypt cell migration and shedding, and is required to constantly replenish the crypt cell population.

Authors+Show Affiliations

School of Biological Sciences, University of East Anglia, Norwich Research Park, , Norwich, Norfolk, UK.No affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Journal Article
Research Support, Non-U.S. Gov't

Language

eng

PubMed ID

23831735

Citation

Reynolds, Amy, et al. "Canonical Wnt Signals Combined With Suppressed TGFβ/BMP Pathways Promote Renewal of the Native Human Colonic Epithelium." Gut, vol. 63, no. 4, 2014, pp. 610-21.
Reynolds A, Wharton N, Parris A, et al. Canonical Wnt signals combined with suppressed TGFβ/BMP pathways promote renewal of the native human colonic epithelium. Gut. 2014;63(4):610-21.
Reynolds, A., Wharton, N., Parris, A., Mitchell, E., Sobolewski, A., Kam, C., Bigwood, L., El Hadi, A., Münsterberg, A., Lewis, M., Speakman, C., Stebbings, W., Wharton, R., Sargen, K., Tighe, R., Jamieson, C., Hernon, J., Kapur, S., Oue, N., ... Williams, M. R. (2014). Canonical Wnt signals combined with suppressed TGFβ/BMP pathways promote renewal of the native human colonic epithelium. Gut, 63(4), 610-21. https://doi.org/10.1136/gutjnl-2012-304067
Reynolds A, et al. Canonical Wnt Signals Combined With Suppressed TGFβ/BMP Pathways Promote Renewal of the Native Human Colonic Epithelium. Gut. 2014;63(4):610-21. PubMed PMID: 23831735.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Canonical Wnt signals combined with suppressed TGFβ/BMP pathways promote renewal of the native human colonic epithelium. AU - Reynolds,Amy, AU - Wharton,Natalia, AU - Parris,Alyson, AU - Mitchell,Esther, AU - Sobolewski,Anastasia, AU - Kam,Christy, AU - Bigwood,Loren, AU - El Hadi,Ahmed, AU - Münsterberg,Andrea, AU - Lewis,Michael, AU - Speakman,Christopher, AU - Stebbings,William, AU - Wharton,Richard, AU - Sargen,Kevin, AU - Tighe,Richard, AU - Jamieson,Crawford, AU - Hernon,James, AU - Kapur,Sandeep, AU - Oue,Naohide, AU - Yasui,Wataru, AU - Williams,Mark R, Y1 - 2013/07/05/ PY - 2013/7/9/entrez PY - 2013/7/9/pubmed PY - 2014/4/24/medline KW - Epithelial Differentiation KW - Epithelial Kinetics KW - Epithelial Proliferation KW - Imaging KW - Stem Cells SP - 610 EP - 21 JF - Gut JO - Gut VL - 63 IS - 4 N2 - BACKGROUND: A defining characteristic of the human intestinal epithelium is that it is the most rapidly renewing tissue in the body. However, the processes underlying tissue renewal and the mechanisms that govern their coordination have proved difficult to study in the human gut. OBJECTIVE: To investigate the regulation of stem cell-driven tissue renewal by canonical Wnt and TGFβ/bone morphogenetic protein (BMP) pathways in the native human colonic epithelium. DESIGN: Intact human colonic crypts were isolated from mucosal tissue samples and placed into 3D culture conditions optimised for steady-state tissue renewal. High affinity mRNA in situ hybridisation and immunohistochemistry were complemented by functional genomic and bioimaging techniques. The effects of signalling pathway modulators on the status of intestinal stem cell biology, crypt cell proliferation, migration, differentiation and shedding were determined. RESULTS: Native human colonic crypts exhibited distinct activation profiles for canonical Wnt, TGFβ and BMP pathways. A population of intestinal LGR5/OLFM4-positive stem/progenitor cells were interspersed between goblet-like cells within the crypt-base. Exogenous and crypt cell-autonomous canonical Wnt signals supported homeostatic intestinal stem/progenitor cell proliferation and were antagonised by TGFβ or BMP pathway activation. Reduced Wnt stimulation impeded crypt cell proliferation, but crypt cell migration and shedding from the crypt surface were unaffected and resulted in diminished crypts. CONCLUSIONS: Steady-state tissue renewal in the native human colonic epithelium is dependent on canonical Wnt signals combined with suppressed TGFβ/BMP pathways. Stem/progenitor cell proliferation is uncoupled from crypt cell migration and shedding, and is required to constantly replenish the crypt cell population. SN - 1468-3288 UR - https://www.unboundmedicine.com/medline/citation/23831735/Canonical_Wnt_signals_combined_with_suppressed_TGF L2 - http://gut.bmj.com/lookup/pmidlookup?view=long&pmid=23831735 DB - PRIME DP - Unbound Medicine ER -