Enteric Nervous System Stem Cells Derived From Human Gut Mucosa for the Treatment of Aganglionic Gut Disorders

Background & Aims Enteric nervous system stem cells (ENSSCs) provide potential therapeutic tools to replenish absent ganglia in Hirschsprung's disease. Although full-thickness human postnatal gut tissue can be used to generate ENSSCs, reliance on its harvesting from surgical resection poses...

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Veröffentlicht in:Gastroenterology (New York, N.Y. 1943) N.Y. 1943), 2009-06, Vol.136 (7), p.2214-2225.e3
Hauptverfasser: Metzger, Marco, Caldwell, Claire, Barlow, Amanda J, Burns, Alan J, Thapar, Nikhil
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container_end_page 2225.e3
container_issue 7
container_start_page 2214
container_title Gastroenterology (New York, N.Y. 1943)
container_volume 136
creator Metzger, Marco
Caldwell, Claire
Barlow, Amanda J
Burns, Alan J
Thapar, Nikhil
description Background & Aims Enteric nervous system stem cells (ENSSCs) provide potential therapeutic tools to replenish absent ganglia in Hirschsprung's disease. Although full-thickness human postnatal gut tissue can be used to generate ENSSCs, reliance on its harvesting from surgical resection poses significant practical limitations. This study aimed to explore whether gut tissue obtained utilizing minimally invasive routine endoscopy techniques could be used to generate ENSSCs and whether such cells retain the potential to generate an ENS upon transplantation into aganglionic gut. Methods Postnatal human gut mucosal tissue obtained from children undergoing gastrointestinal endoscopy was used to generate cell cultures in which ENSSCs were contained within neurosphere-like bodies (NLBs). These NLBs were characterized by immunostaining, and their potential to generate components of the ENS, in vitro and upon transplantation into models of aganglionic gut, was examined. Results Gut mucosal biopsy specimens were obtained from 75 children (age, 9 months–17 years). The biopsy specimens contained neural cells and ENSSCs and, on culturing, generated characteristic NLBs at all ages examined. Postnatal mucosa-derived NLBs contained cells that, akin to their embryonic counterparts, were proliferating, expressed ENSSC markers, were bipotent, and capable of generating large colonies in clonogenic cultures and multiple ENS neuronal subtypes. Upon transplantation, cells from NLBs colonized cultured recipient aganglionic chick and human hindgut to generate ganglia-like structures and enteric neurons and glia. Conclusions The results represent a significant practical advance toward the development of definitive cell replenishment therapies for ENS disorders such as Hirschsprung's disease.
doi_str_mv 10.1053/j.gastro.2009.02.048
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Although full-thickness human postnatal gut tissue can be used to generate ENSSCs, reliance on its harvesting from surgical resection poses significant practical limitations. This study aimed to explore whether gut tissue obtained utilizing minimally invasive routine endoscopy techniques could be used to generate ENSSCs and whether such cells retain the potential to generate an ENS upon transplantation into aganglionic gut. Methods Postnatal human gut mucosal tissue obtained from children undergoing gastrointestinal endoscopy was used to generate cell cultures in which ENSSCs were contained within neurosphere-like bodies (NLBs). These NLBs were characterized by immunostaining, and their potential to generate components of the ENS, in vitro and upon transplantation into models of aganglionic gut, was examined. Results Gut mucosal biopsy specimens were obtained from 75 children (age, 9 months–17 years). The biopsy specimens contained neural cells and ENSSCs and, on culturing, generated characteristic NLBs at all ages examined. Postnatal mucosa-derived NLBs contained cells that, akin to their embryonic counterparts, were proliferating, expressed ENSSC markers, were bipotent, and capable of generating large colonies in clonogenic cultures and multiple ENS neuronal subtypes. Upon transplantation, cells from NLBs colonized cultured recipient aganglionic chick and human hindgut to generate ganglia-like structures and enteric neurons and glia. Conclusions The results represent a significant practical advance toward the development of definitive cell replenishment therapies for ENS disorders such as Hirschsprung's disease.</description><identifier>ISSN: 0016-5085</identifier><identifier>EISSN: 1528-0012</identifier><identifier>DOI: 10.1053/j.gastro.2009.02.048</identifier><identifier>PMID: 19505425</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Adolescent ; Cell Proliferation ; Cells, Cultured ; Child ; Child, Preschool ; Enteric Nervous System - cytology ; Enteric Nervous System - embryology ; Female ; Gastroenterology and Hepatology ; Gastrointestinal Tract - cytology ; Gastrointestinal Tract - physiology ; Hirschsprung Disease - pathology ; Hirschsprung Disease - therapy ; Humans ; Infant ; Intestinal Mucosa - cytology ; Intestinal Mucosa - transplantation ; Male ; Microscopy, Fluorescence ; Mucous Membrane - transplantation ; Regeneration ; Sampling Studies ; Sensitivity and Specificity ; Stem Cell Transplantation - methods</subject><ispartof>Gastroenterology (New York, N.Y. 1943), 2009-06, Vol.136 (7), p.2214-2225.e3</ispartof><rights>AGA Institute</rights><rights>2009 AGA Institute</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c461t-2ea50539815fdd8c7e5b9867376393e6d2c5caea7a329e13e513d241ce5213d83</citedby><cites>FETCH-LOGICAL-c461t-2ea50539815fdd8c7e5b9867376393e6d2c5caea7a329e13e513d241ce5213d83</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1053/j.gastro.2009.02.048$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3548,27923,27924,45994</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19505425$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Metzger, Marco</creatorcontrib><creatorcontrib>Caldwell, Claire</creatorcontrib><creatorcontrib>Barlow, Amanda J</creatorcontrib><creatorcontrib>Burns, Alan J</creatorcontrib><creatorcontrib>Thapar, Nikhil</creatorcontrib><title>Enteric Nervous System Stem Cells Derived From Human Gut Mucosa for the Treatment of Aganglionic Gut Disorders</title><title>Gastroenterology (New York, N.Y. 1943)</title><addtitle>Gastroenterology</addtitle><description>Background &amp; Aims Enteric nervous system stem cells (ENSSCs) provide potential therapeutic tools to replenish absent ganglia in Hirschsprung's disease. Although full-thickness human postnatal gut tissue can be used to generate ENSSCs, reliance on its harvesting from surgical resection poses significant practical limitations. This study aimed to explore whether gut tissue obtained utilizing minimally invasive routine endoscopy techniques could be used to generate ENSSCs and whether such cells retain the potential to generate an ENS upon transplantation into aganglionic gut. Methods Postnatal human gut mucosal tissue obtained from children undergoing gastrointestinal endoscopy was used to generate cell cultures in which ENSSCs were contained within neurosphere-like bodies (NLBs). These NLBs were characterized by immunostaining, and their potential to generate components of the ENS, in vitro and upon transplantation into models of aganglionic gut, was examined. Results Gut mucosal biopsy specimens were obtained from 75 children (age, 9 months–17 years). The biopsy specimens contained neural cells and ENSSCs and, on culturing, generated characteristic NLBs at all ages examined. Postnatal mucosa-derived NLBs contained cells that, akin to their embryonic counterparts, were proliferating, expressed ENSSC markers, were bipotent, and capable of generating large colonies in clonogenic cultures and multiple ENS neuronal subtypes. Upon transplantation, cells from NLBs colonized cultured recipient aganglionic chick and human hindgut to generate ganglia-like structures and enteric neurons and glia. 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Caldwell, Claire ; Barlow, Amanda J ; Burns, Alan J ; Thapar, Nikhil</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c461t-2ea50539815fdd8c7e5b9867376393e6d2c5caea7a329e13e513d241ce5213d83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Adolescent</topic><topic>Cell Proliferation</topic><topic>Cells, Cultured</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Enteric Nervous System - cytology</topic><topic>Enteric Nervous System - embryology</topic><topic>Female</topic><topic>Gastroenterology and Hepatology</topic><topic>Gastrointestinal Tract - cytology</topic><topic>Gastrointestinal Tract - physiology</topic><topic>Hirschsprung Disease - pathology</topic><topic>Hirschsprung Disease - therapy</topic><topic>Humans</topic><topic>Infant</topic><topic>Intestinal Mucosa - cytology</topic><topic>Intestinal Mucosa - transplantation</topic><topic>Male</topic><topic>Microscopy, Fluorescence</topic><topic>Mucous Membrane - transplantation</topic><topic>Regeneration</topic><topic>Sampling Studies</topic><topic>Sensitivity and Specificity</topic><topic>Stem Cell Transplantation - methods</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Metzger, Marco</creatorcontrib><creatorcontrib>Caldwell, Claire</creatorcontrib><creatorcontrib>Barlow, Amanda J</creatorcontrib><creatorcontrib>Burns, Alan J</creatorcontrib><creatorcontrib>Thapar, Nikhil</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Gastroenterology (New York, N.Y. 1943)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Metzger, Marco</au><au>Caldwell, Claire</au><au>Barlow, Amanda J</au><au>Burns, Alan J</au><au>Thapar, Nikhil</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Enteric Nervous System Stem Cells Derived From Human Gut Mucosa for the Treatment of Aganglionic Gut Disorders</atitle><jtitle>Gastroenterology (New York, N.Y. 1943)</jtitle><addtitle>Gastroenterology</addtitle><date>2009-06-01</date><risdate>2009</risdate><volume>136</volume><issue>7</issue><spage>2214</spage><epage>2225.e3</epage><pages>2214-2225.e3</pages><issn>0016-5085</issn><eissn>1528-0012</eissn><abstract>Background &amp; Aims Enteric nervous system stem cells (ENSSCs) provide potential therapeutic tools to replenish absent ganglia in Hirschsprung's disease. Although full-thickness human postnatal gut tissue can be used to generate ENSSCs, reliance on its harvesting from surgical resection poses significant practical limitations. This study aimed to explore whether gut tissue obtained utilizing minimally invasive routine endoscopy techniques could be used to generate ENSSCs and whether such cells retain the potential to generate an ENS upon transplantation into aganglionic gut. Methods Postnatal human gut mucosal tissue obtained from children undergoing gastrointestinal endoscopy was used to generate cell cultures in which ENSSCs were contained within neurosphere-like bodies (NLBs). These NLBs were characterized by immunostaining, and their potential to generate components of the ENS, in vitro and upon transplantation into models of aganglionic gut, was examined. Results Gut mucosal biopsy specimens were obtained from 75 children (age, 9 months–17 years). The biopsy specimens contained neural cells and ENSSCs and, on culturing, generated characteristic NLBs at all ages examined. Postnatal mucosa-derived NLBs contained cells that, akin to their embryonic counterparts, were proliferating, expressed ENSSC markers, were bipotent, and capable of generating large colonies in clonogenic cultures and multiple ENS neuronal subtypes. Upon transplantation, cells from NLBs colonized cultured recipient aganglionic chick and human hindgut to generate ganglia-like structures and enteric neurons and glia. Conclusions The results represent a significant practical advance toward the development of definitive cell replenishment therapies for ENS disorders such as Hirschsprung's disease.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>19505425</pmid><doi>10.1053/j.gastro.2009.02.048</doi><oa>free_for_read</oa></addata></record>
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subjects Adolescent
Cell Proliferation
Cells, Cultured
Child
Child, Preschool
Enteric Nervous System - cytology
Enteric Nervous System - embryology
Female
Gastroenterology and Hepatology
Gastrointestinal Tract - cytology
Gastrointestinal Tract - physiology
Hirschsprung Disease - pathology
Hirschsprung Disease - therapy
Humans
Infant
Intestinal Mucosa - cytology
Intestinal Mucosa - transplantation
Male
Microscopy, Fluorescence
Mucous Membrane - transplantation
Regeneration
Sampling Studies
Sensitivity and Specificity
Stem Cell Transplantation - methods
title Enteric Nervous System Stem Cells Derived From Human Gut Mucosa for the Treatment of Aganglionic Gut Disorders
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