Journal Article
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Gut
Gut
Jan
64
1
11
19
LR: 20160713; CI: Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions.; GR: 092096/Wellcome Trust/United Kingdom; GR: 098357/
England
1468-3288; 0017-5749
PMID: 24572143
eng
Journal Article; Research Support, Non-U.S. Gov't; AIM; IM
10.1136/gutjnl-2013-306171 [doi]
Unknown(0)
24572143
OBJECTIVE: Knowledge of the cellular mechanisms involved in homeostasis of human squamous oesophagus in the steady state and following chronic injury is limited. We aimed to better understand these mechanisms by using a functional 3D approach. DESIGN: Proliferation, mitosis and the expression of progenitor lineage markers were assessed in normal squamous oesophagus from 10 patients by immunofluorescence on 3D epithelial whole mounts. Cells expressing differential levels of epithelial and progenitor markers were isolated using flow cytometry sorting and characterised by qPCR and IF. Their self-renewing potential was investigated by colony forming cells assays and in vitro organotypic culture models. RESULTS: Proliferation and mitotic activity was highest in the interpapillary basal layer and decreased linearly towards the tip of the papilla (p
Barbera,M., di Pietro,M., Walker,E., Brierley,C., MacRae,S., Simons,B.D., Jones,P.H., Stingl,J., Fitzgerald,R.C.
MRC Cancer Unit, University of Cambridge Cambridge, UK.; MRC Cancer Unit, University of Cambridge Cambridge, UK.; MRC Cancer Unit, University of Cambridge Cambridge, UK.; MRC Cancer Unit, University of Cambridge Cambridge, UK.; MRC Cancer Unit, University
20140226
PMC4283695
http://vp9py7xf3h.search.serialssolutions.com/?charset=utf-8&pmid=24572143
2015