Evaluation of ES-derived neural progenitors as a potential source for cell replacement therapy in the gut

<p>Abstract</p> <p>Background</p> <p>Stem cell-based therapy has recently been explored for the treatment of disorders of the enteric nervous system (ENS). Pluripotent embryonic stem (ES) cells represent an attractive cell source; however, little or no information is cu...

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Main Authors: Sasselli Valentina, Micci Maria-Adelaide, Kahrig Kristen M, Pasricha Pankaj
Format: Article
Language:English
Published: BMC 2012-06-01
Series:BMC Gastroenterology
Subjects:
Online Access:http://www.biomedcentral.com/1471-230X/12/81
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spelling doaj-1d6c08d41faf4f069976d1702db92b0e2020-11-25T03:25:09ZengBMCBMC Gastroenterology1471-230X2012-06-011218110.1186/1471-230X-12-81Evaluation of ES-derived neural progenitors as a potential source for cell replacement therapy in the gutSasselli ValentinaMicci Maria-AdelaideKahrig Kristen MPasricha Pankaj<p>Abstract</p> <p>Background</p> <p>Stem cell-based therapy has recently been explored for the treatment of disorders of the enteric nervous system (ENS). Pluripotent embryonic stem (ES) cells represent an attractive cell source; however, little or no information is currently available on how ES cells will respond to the gut environment. In this study, we investigated the ability of ES cells to respond to environmental cues derived from the ENS and related tissues, both <it>in vitro</it> and <it>in vivo</it>.</p> <p>Methods</p> <p>Neurospheres were generated from mouse ES cells (ES-NS) and co-cultured with organotypic preparations of gut tissue consisting of the longitudinal muscle layers with the adherent myenteric plexus (LM-MP).</p> <p>Results</p> <p>LM-MP co-culture led to a significant increase in the expression of pan-neuronal markers (βIII-tubulin, PGP 9.5) as well as more specialized markers (peripherin, nNOS) in ES-NS, both at the transcriptional and protein level. The increased expression was not associated with increased proliferation, thus confirming a true neurogenic effect. LM-MP preparations exerted also a myogenic effect on ES-NS, although to a lesser extent. After transplantation <it>in vivo</it> into the mouse pylorus, grafted ES-NS failed to acquire a distinct phenotype al least 1 week following transplantation.</p> <p>Conclusions</p> <p>This is the first study reporting that the gut explants can induce neuronal differentiation of ES cells <it>in vitro</it> and induce the expression of nNOS, a key molecule in gastrointestinal motility regulation. The inability of ES-NS to adopt a neuronal phenotype after transplantation in the gastrointestinal tract is suggestive of the presence of local inhibitory influences that prevent ES-NS differentiation <it>in vivo</it>.</p> http://www.biomedcentral.com/1471-230X/12/81Embryonic stem cellsEnteric nervous systemGastrointestinal motilityStem cell transplantation
collection DOAJ
language English
format Article
sources DOAJ
author Sasselli Valentina
Micci Maria-Adelaide
Kahrig Kristen M
Pasricha Pankaj
spellingShingle Sasselli Valentina
Micci Maria-Adelaide
Kahrig Kristen M
Pasricha Pankaj
Evaluation of ES-derived neural progenitors as a potential source for cell replacement therapy in the gut
BMC Gastroenterology
Embryonic stem cells
Enteric nervous system
Gastrointestinal motility
Stem cell transplantation
author_facet Sasselli Valentina
Micci Maria-Adelaide
Kahrig Kristen M
Pasricha Pankaj
author_sort Sasselli Valentina
title Evaluation of ES-derived neural progenitors as a potential source for cell replacement therapy in the gut
title_short Evaluation of ES-derived neural progenitors as a potential source for cell replacement therapy in the gut
title_full Evaluation of ES-derived neural progenitors as a potential source for cell replacement therapy in the gut
title_fullStr Evaluation of ES-derived neural progenitors as a potential source for cell replacement therapy in the gut
title_full_unstemmed Evaluation of ES-derived neural progenitors as a potential source for cell replacement therapy in the gut
title_sort evaluation of es-derived neural progenitors as a potential source for cell replacement therapy in the gut
publisher BMC
series BMC Gastroenterology
issn 1471-230X
publishDate 2012-06-01
description <p>Abstract</p> <p>Background</p> <p>Stem cell-based therapy has recently been explored for the treatment of disorders of the enteric nervous system (ENS). Pluripotent embryonic stem (ES) cells represent an attractive cell source; however, little or no information is currently available on how ES cells will respond to the gut environment. In this study, we investigated the ability of ES cells to respond to environmental cues derived from the ENS and related tissues, both <it>in vitro</it> and <it>in vivo</it>.</p> <p>Methods</p> <p>Neurospheres were generated from mouse ES cells (ES-NS) and co-cultured with organotypic preparations of gut tissue consisting of the longitudinal muscle layers with the adherent myenteric plexus (LM-MP).</p> <p>Results</p> <p>LM-MP co-culture led to a significant increase in the expression of pan-neuronal markers (βIII-tubulin, PGP 9.5) as well as more specialized markers (peripherin, nNOS) in ES-NS, both at the transcriptional and protein level. The increased expression was not associated with increased proliferation, thus confirming a true neurogenic effect. LM-MP preparations exerted also a myogenic effect on ES-NS, although to a lesser extent. After transplantation <it>in vivo</it> into the mouse pylorus, grafted ES-NS failed to acquire a distinct phenotype al least 1 week following transplantation.</p> <p>Conclusions</p> <p>This is the first study reporting that the gut explants can induce neuronal differentiation of ES cells <it>in vitro</it> and induce the expression of nNOS, a key molecule in gastrointestinal motility regulation. The inability of ES-NS to adopt a neuronal phenotype after transplantation in the gastrointestinal tract is suggestive of the presence of local inhibitory influences that prevent ES-NS differentiation <it>in vivo</it>.</p>
topic Embryonic stem cells
Enteric nervous system
Gastrointestinal motility
Stem cell transplantation
url http://www.biomedcentral.com/1471-230X/12/81
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