Distinct human stem cell populations in small and large intestine.

The intestine is composed of an epithelial layer containing rapidly proliferating cells that mature into two regions, the small and the large intestine. Although previous studies have identified stem cells as the cell-of-origin for intestinal epithelial cells, no studies have directly compared stem...

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Main Authors: Julie M Cramer, Timothy Thompson, Albert Geskin, William LaFramboise, Eric Lagasse
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2015-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC4353627?pdf=render
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spelling doaj-feb346bea8d04cbc88df1b496518e15e2020-11-25T02:32:57ZengPublic Library of Science (PLoS)PLoS ONE1932-62032015-01-01103e011879210.1371/journal.pone.0118792Distinct human stem cell populations in small and large intestine.Julie M CramerTimothy ThompsonAlbert GeskinWilliam LaFramboiseEric LagasseThe intestine is composed of an epithelial layer containing rapidly proliferating cells that mature into two regions, the small and the large intestine. Although previous studies have identified stem cells as the cell-of-origin for intestinal epithelial cells, no studies have directly compared stem cells derived from these anatomically distinct regions. Here, we examine intrinsic differences between primary epithelial cells isolated from human fetal small and large intestine, after in vitro expansion, using the Wnt agonist R-spondin 2. We utilized flow cytometry, fluorescence-activated cell sorting, gene expression analysis and a three-dimensional in vitro differentiation assay to characterize their stem cell properties. We identified stem cell markers that separate subpopulations of colony-forming cells in the small and large intestine and revealed important differences in differentiation, proliferation and disease pathways using gene expression analysis. Single cells from small and large intestine cultures formed organoids that reflect the distinct cellular hierarchy found in vivo and respond differently to identical exogenous cues. Our characterization identified numerous differences between small and large intestine epithelial stem cells suggesting possible connections to intestinal disease.http://europepmc.org/articles/PMC4353627?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Julie M Cramer
Timothy Thompson
Albert Geskin
William LaFramboise
Eric Lagasse
spellingShingle Julie M Cramer
Timothy Thompson
Albert Geskin
William LaFramboise
Eric Lagasse
Distinct human stem cell populations in small and large intestine.
PLoS ONE
author_facet Julie M Cramer
Timothy Thompson
Albert Geskin
William LaFramboise
Eric Lagasse
author_sort Julie M Cramer
title Distinct human stem cell populations in small and large intestine.
title_short Distinct human stem cell populations in small and large intestine.
title_full Distinct human stem cell populations in small and large intestine.
title_fullStr Distinct human stem cell populations in small and large intestine.
title_full_unstemmed Distinct human stem cell populations in small and large intestine.
title_sort distinct human stem cell populations in small and large intestine.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2015-01-01
description The intestine is composed of an epithelial layer containing rapidly proliferating cells that mature into two regions, the small and the large intestine. Although previous studies have identified stem cells as the cell-of-origin for intestinal epithelial cells, no studies have directly compared stem cells derived from these anatomically distinct regions. Here, we examine intrinsic differences between primary epithelial cells isolated from human fetal small and large intestine, after in vitro expansion, using the Wnt agonist R-spondin 2. We utilized flow cytometry, fluorescence-activated cell sorting, gene expression analysis and a three-dimensional in vitro differentiation assay to characterize their stem cell properties. We identified stem cell markers that separate subpopulations of colony-forming cells in the small and large intestine and revealed important differences in differentiation, proliferation and disease pathways using gene expression analysis. Single cells from small and large intestine cultures formed organoids that reflect the distinct cellular hierarchy found in vivo and respond differently to identical exogenous cues. Our characterization identified numerous differences between small and large intestine epithelial stem cells suggesting possible connections to intestinal disease.
url http://europepmc.org/articles/PMC4353627?pdf=render
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