Intestitial Cells of Cajal in the Human Small Intestine: Immunochemical and Ultrastructural Study

The stem cell kinase CD117 has recently been found to play an important role in the development of interstitial cells of Cajal (ICC), which are currently regarded as pacemaker cells of the gastrointestinal tract. CD117 is expressed in both gastrointestinal stromal tumors (GIST) and ICC, with the lat...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Ultrastructural pathology 2003-03, Vol.27 (2), p.67-78
Hauptverfasser: Min, Kyung-Whan, Sook Seo, In
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 78
container_issue 2
container_start_page 67
container_title Ultrastructural pathology
container_volume 27
creator Min, Kyung-Whan
Sook Seo, In
description The stem cell kinase CD117 has recently been found to play an important role in the development of interstitial cells of Cajal (ICC), which are currently regarded as pacemaker cells of the gastrointestinal tract. CD117 is expressed in both gastrointestinal stromal tumors (GIST) and ICC, with the latter regarded by many as the progenitor cells of GIST. The authors investigated immunoreactivity of 25 normal surgically removed small intestinal tissues and correlated the findings with electron microscopy (EM) on 12 cases. In all cases CD117-positive cells were frequently seen around the myenteric plexi either singly or in groups. CD117-positive cells on immunostained sections corresponded to the cells appearing as fibroblast-like or undifferentiated primitive mesenchymal cells around the myenteric ganglia and interstitial spaces by EM. In contrast, S-100 stain revealed a fine network of positive staining throughout the muscularis. Branches of nonmyelinated axons and nerve endings were found regularly between myocytes with direct contact with muscle cells by EM. The cells that we could depict as ICC because of their distribution andstaining pattern of CD117 were limited to the nonmuscular mesenchymal cells. No muscle cell-like ICC were found. Instead, the muscle cells in direct contact with nerve endings were often disfigured and the cytoarchitectural contents for muscle cells became less distinct because of lighter staining and loss of definite focal densities among actin filaments. However, these latter cells did maintain most muscle cell features, such as continuous external lamina, caveolae, and some of the peripheral densities. These findings raise a possibility that previous investigators could have included these altered muscle cells into the ICC group. It was also found that intestinal muscularis not only was richly endowed with an elaborate neural network of delicate axonal extensions and dense-core granule containing nerve endings traversing through and between myocytes, but also showed frequent synapse-like direct contact between nerve endings and muscle cells. These findings indicate that enteric nerves may play a major role in the control of intestinal motility, while CD117-positive cells play an accessory role as cells of Cajal as originally speculated. Further studies are necessary to better define and characterize interstitial cells of Cajal, which will be useful in the correlation of the vast number of data concerning the possible role of CD117
doi_str_mv 10.1080/01913120309927
format Article
fullrecord <record><control><sourceid>proquest_infor</sourceid><recordid>TN_cdi_informahealthcare_journals_10_1080_01913120309927</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>73307455</sourcerecordid><originalsourceid>FETCH-LOGICAL-c390t-5f50facb487db3f247e163535819cde9e187936a0147bcbf56257d02a9ac84043</originalsourceid><addsrcrecordid>eNp1kM2LFDEQxYMo7rh69Sg5eeu10ulMOt5kUHdgwcO651CdTpge8rEmaWT-e7PMgOxhT0VV_erx6hHykcENgxG-AFOMsx44KNXLV2TDRM86kGJ8TTZPy65t-RV5V8oRAASH8S25Yr0ctkzJDcF9rLbUpS7o6c56X2hydIfH1i6R1oOlt2vASO8Dek8vdLRf6T6ENSZzsGExDcY40wdfM5aaV1PX3Gb3dZ1P78kbh77YD5d6TR5-fP-9u-3ufv3c777ddYYrqJ1wAhyaaRjlPHHXD9KyLRdcjEyZ2SrLRqn4FoENcjKTE9teyBl6VGjGAQZ-TT6fdR9z-rM2lzosxbSPMNq0Fi05BzkI0cCbM2hyKiVbpx_zEjCfNAP9FKp-Hmo7-HRRXqdg5__4JcUGqDOwRJdywL8p-1lXPPmUXcZolqL5i-Ljs9uDRV8PBrPVx7Tm2CJ7ydc_XemVhw</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>73307455</pqid></control><display><type>article</type><title>Intestitial Cells of Cajal in the Human Small Intestine: Immunochemical and Ultrastructural Study</title><source>MEDLINE</source><source>Taylor &amp; Francis Medical Library - CRKN</source><source>Taylor &amp; Francis Journals Complete</source><creator>Min, Kyung-Whan ; Sook Seo, In</creator><creatorcontrib>Min, Kyung-Whan ; Sook Seo, In</creatorcontrib><description>The stem cell kinase CD117 has recently been found to play an important role in the development of interstitial cells of Cajal (ICC), which are currently regarded as pacemaker cells of the gastrointestinal tract. CD117 is expressed in both gastrointestinal stromal tumors (GIST) and ICC, with the latter regarded by many as the progenitor cells of GIST. The authors investigated immunoreactivity of 25 normal surgically removed small intestinal tissues and correlated the findings with electron microscopy (EM) on 12 cases. In all cases CD117-positive cells were frequently seen around the myenteric plexi either singly or in groups. CD117-positive cells on immunostained sections corresponded to the cells appearing as fibroblast-like or undifferentiated primitive mesenchymal cells around the myenteric ganglia and interstitial spaces by EM. In contrast, S-100 stain revealed a fine network of positive staining throughout the muscularis. Branches of nonmyelinated axons and nerve endings were found regularly between myocytes with direct contact with muscle cells by EM. The cells that we could depict as ICC because of their distribution andstaining pattern of CD117 were limited to the nonmuscular mesenchymal cells. No muscle cell-like ICC were found. Instead, the muscle cells in direct contact with nerve endings were often disfigured and the cytoarchitectural contents for muscle cells became less distinct because of lighter staining and loss of definite focal densities among actin filaments. However, these latter cells did maintain most muscle cell features, such as continuous external lamina, caveolae, and some of the peripheral densities. These findings raise a possibility that previous investigators could have included these altered muscle cells into the ICC group. It was also found that intestinal muscularis not only was richly endowed with an elaborate neural network of delicate axonal extensions and dense-core granule containing nerve endings traversing through and between myocytes, but also showed frequent synapse-like direct contact between nerve endings and muscle cells. These findings indicate that enteric nerves may play a major role in the control of intestinal motility, while CD117-positive cells play an accessory role as cells of Cajal as originally speculated. Further studies are necessary to better define and characterize interstitial cells of Cajal, which will be useful in the correlation of the vast number of data concerning the possible role of CD117-positive ICC in the pacemaker function of the intestine and oncogenesis of GIST.</description><identifier>ISSN: 0191-3123</identifier><identifier>EISSN: 1521-0758</identifier><identifier>DOI: 10.1080/01913120309927</identifier><identifier>PMID: 12746197</identifier><language>eng</language><publisher>England: Informa UK Ltd</publisher><subject>Adult ; Female ; Humans ; Immunohistochemistry ; Intestine, Small - innervation ; Intestine, Small - metabolism ; Intestine, Small - ultrastructure ; Male ; Microscopy, Electron ; Myenteric Plexus - metabolism ; Myenteric Plexus - ultrastructure ; Proto-Oncogene Proteins c-kit - metabolism ; Stromal Cells - metabolism ; Stromal Cells - ultrastructure</subject><ispartof>Ultrastructural pathology, 2003-03, Vol.27 (2), p.67-78</ispartof><rights>2003 Informa UK Ltd All rights reserved: reproduction in whole or part not permitted 2003</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c390t-5f50facb487db3f247e163535819cde9e187936a0147bcbf56257d02a9ac84043</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.tandfonline.com/doi/pdf/10.1080/01913120309927$$EPDF$$P50$$Ginformaworld$$H</linktopdf><linktohtml>$$Uhttps://www.tandfonline.com/doi/full/10.1080/01913120309927$$EHTML$$P50$$Ginformaworld$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,59647,59753,60436,60542,61221,61256,61402,61437</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12746197$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Min, Kyung-Whan</creatorcontrib><creatorcontrib>Sook Seo, In</creatorcontrib><title>Intestitial Cells of Cajal in the Human Small Intestine: Immunochemical and Ultrastructural Study</title><title>Ultrastructural pathology</title><addtitle>Ultrastruct Pathol</addtitle><description>The stem cell kinase CD117 has recently been found to play an important role in the development of interstitial cells of Cajal (ICC), which are currently regarded as pacemaker cells of the gastrointestinal tract. CD117 is expressed in both gastrointestinal stromal tumors (GIST) and ICC, with the latter regarded by many as the progenitor cells of GIST. The authors investigated immunoreactivity of 25 normal surgically removed small intestinal tissues and correlated the findings with electron microscopy (EM) on 12 cases. In all cases CD117-positive cells were frequently seen around the myenteric plexi either singly or in groups. CD117-positive cells on immunostained sections corresponded to the cells appearing as fibroblast-like or undifferentiated primitive mesenchymal cells around the myenteric ganglia and interstitial spaces by EM. In contrast, S-100 stain revealed a fine network of positive staining throughout the muscularis. Branches of nonmyelinated axons and nerve endings were found regularly between myocytes with direct contact with muscle cells by EM. The cells that we could depict as ICC because of their distribution andstaining pattern of CD117 were limited to the nonmuscular mesenchymal cells. No muscle cell-like ICC were found. Instead, the muscle cells in direct contact with nerve endings were often disfigured and the cytoarchitectural contents for muscle cells became less distinct because of lighter staining and loss of definite focal densities among actin filaments. However, these latter cells did maintain most muscle cell features, such as continuous external lamina, caveolae, and some of the peripheral densities. These findings raise a possibility that previous investigators could have included these altered muscle cells into the ICC group. It was also found that intestinal muscularis not only was richly endowed with an elaborate neural network of delicate axonal extensions and dense-core granule containing nerve endings traversing through and between myocytes, but also showed frequent synapse-like direct contact between nerve endings and muscle cells. These findings indicate that enteric nerves may play a major role in the control of intestinal motility, while CD117-positive cells play an accessory role as cells of Cajal as originally speculated. Further studies are necessary to better define and characterize interstitial cells of Cajal, which will be useful in the correlation of the vast number of data concerning the possible role of CD117-positive ICC in the pacemaker function of the intestine and oncogenesis of GIST.</description><subject>Adult</subject><subject>Female</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>Intestine, Small - innervation</subject><subject>Intestine, Small - metabolism</subject><subject>Intestine, Small - ultrastructure</subject><subject>Male</subject><subject>Microscopy, Electron</subject><subject>Myenteric Plexus - metabolism</subject><subject>Myenteric Plexus - ultrastructure</subject><subject>Proto-Oncogene Proteins c-kit - metabolism</subject><subject>Stromal Cells - metabolism</subject><subject>Stromal Cells - ultrastructure</subject><issn>0191-3123</issn><issn>1521-0758</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kM2LFDEQxYMo7rh69Sg5eeu10ulMOt5kUHdgwcO651CdTpge8rEmaWT-e7PMgOxhT0VV_erx6hHykcENgxG-AFOMsx44KNXLV2TDRM86kGJ8TTZPy65t-RV5V8oRAASH8S25Yr0ctkzJDcF9rLbUpS7o6c56X2hydIfH1i6R1oOlt2vASO8Dek8vdLRf6T6ENSZzsGExDcY40wdfM5aaV1PX3Gb3dZ1P78kbh77YD5d6TR5-fP-9u-3ufv3c777ddYYrqJ1wAhyaaRjlPHHXD9KyLRdcjEyZ2SrLRqn4FoENcjKTE9teyBl6VGjGAQZ-TT6fdR9z-rM2lzosxbSPMNq0Fi05BzkI0cCbM2hyKiVbpx_zEjCfNAP9FKp-Hmo7-HRRXqdg5__4JcUGqDOwRJdywL8p-1lXPPmUXcZolqL5i-Ljs9uDRV8PBrPVx7Tm2CJ7ydc_XemVhw</recordid><startdate>20030301</startdate><enddate>20030301</enddate><creator>Min, Kyung-Whan</creator><creator>Sook Seo, In</creator><general>Informa UK Ltd</general><general>Taylor &amp; Francis</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20030301</creationdate><title>Intestitial Cells of Cajal in the Human Small Intestine: Immunochemical and Ultrastructural Study</title><author>Min, Kyung-Whan ; Sook Seo, In</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c390t-5f50facb487db3f247e163535819cde9e187936a0147bcbf56257d02a9ac84043</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>Adult</topic><topic>Female</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>Intestine, Small - innervation</topic><topic>Intestine, Small - metabolism</topic><topic>Intestine, Small - ultrastructure</topic><topic>Male</topic><topic>Microscopy, Electron</topic><topic>Myenteric Plexus - metabolism</topic><topic>Myenteric Plexus - ultrastructure</topic><topic>Proto-Oncogene Proteins c-kit - metabolism</topic><topic>Stromal Cells - metabolism</topic><topic>Stromal Cells - ultrastructure</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Min, Kyung-Whan</creatorcontrib><creatorcontrib>Sook Seo, In</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>Ultrastructural pathology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Min, Kyung-Whan</au><au>Sook Seo, In</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Intestitial Cells of Cajal in the Human Small Intestine: Immunochemical and Ultrastructural Study</atitle><jtitle>Ultrastructural pathology</jtitle><addtitle>Ultrastruct Pathol</addtitle><date>2003-03-01</date><risdate>2003</risdate><volume>27</volume><issue>2</issue><spage>67</spage><epage>78</epage><pages>67-78</pages><issn>0191-3123</issn><eissn>1521-0758</eissn><abstract>The stem cell kinase CD117 has recently been found to play an important role in the development of interstitial cells of Cajal (ICC), which are currently regarded as pacemaker cells of the gastrointestinal tract. CD117 is expressed in both gastrointestinal stromal tumors (GIST) and ICC, with the latter regarded by many as the progenitor cells of GIST. The authors investigated immunoreactivity of 25 normal surgically removed small intestinal tissues and correlated the findings with electron microscopy (EM) on 12 cases. In all cases CD117-positive cells were frequently seen around the myenteric plexi either singly or in groups. CD117-positive cells on immunostained sections corresponded to the cells appearing as fibroblast-like or undifferentiated primitive mesenchymal cells around the myenteric ganglia and interstitial spaces by EM. In contrast, S-100 stain revealed a fine network of positive staining throughout the muscularis. Branches of nonmyelinated axons and nerve endings were found regularly between myocytes with direct contact with muscle cells by EM. The cells that we could depict as ICC because of their distribution andstaining pattern of CD117 were limited to the nonmuscular mesenchymal cells. No muscle cell-like ICC were found. Instead, the muscle cells in direct contact with nerve endings were often disfigured and the cytoarchitectural contents for muscle cells became less distinct because of lighter staining and loss of definite focal densities among actin filaments. However, these latter cells did maintain most muscle cell features, such as continuous external lamina, caveolae, and some of the peripheral densities. These findings raise a possibility that previous investigators could have included these altered muscle cells into the ICC group. It was also found that intestinal muscularis not only was richly endowed with an elaborate neural network of delicate axonal extensions and dense-core granule containing nerve endings traversing through and between myocytes, but also showed frequent synapse-like direct contact between nerve endings and muscle cells. These findings indicate that enteric nerves may play a major role in the control of intestinal motility, while CD117-positive cells play an accessory role as cells of Cajal as originally speculated. Further studies are necessary to better define and characterize interstitial cells of Cajal, which will be useful in the correlation of the vast number of data concerning the possible role of CD117-positive ICC in the pacemaker function of the intestine and oncogenesis of GIST.</abstract><cop>England</cop><pub>Informa UK Ltd</pub><pmid>12746197</pmid><doi>10.1080/01913120309927</doi><tpages>12</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0191-3123
ispartof Ultrastructural pathology, 2003-03, Vol.27 (2), p.67-78
issn 0191-3123
1521-0758
language eng
recordid cdi_informahealthcare_journals_10_1080_01913120309927
source MEDLINE; Taylor & Francis Medical Library - CRKN; Taylor & Francis Journals Complete
subjects Adult
Female
Humans
Immunohistochemistry
Intestine, Small - innervation
Intestine, Small - metabolism
Intestine, Small - ultrastructure
Male
Microscopy, Electron
Myenteric Plexus - metabolism
Myenteric Plexus - ultrastructure
Proto-Oncogene Proteins c-kit - metabolism
Stromal Cells - metabolism
Stromal Cells - ultrastructure
title Intestitial Cells of Cajal in the Human Small Intestine: Immunochemical and Ultrastructural Study
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-05T10%3A04%3A48IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_infor&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Intestitial%20Cells%20of%20Cajal%20in%20the%20Human%20Small%20Intestine:%20Immunochemical%20and%20Ultrastructural%20Study&rft.jtitle=Ultrastructural%20pathology&rft.au=Min,%20Kyung-Whan&rft.date=2003-03-01&rft.volume=27&rft.issue=2&rft.spage=67&rft.epage=78&rft.pages=67-78&rft.issn=0191-3123&rft.eissn=1521-0758&rft_id=info:doi/10.1080/01913120309927&rft_dat=%3Cproquest_infor%3E73307455%3C/proquest_infor%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=73307455&rft_id=info:pmid/12746197&rfr_iscdi=true