Cargando…

Telocytes in Crohn’s disease

Crohn’s disease (CD) is a relapsing chronic inflammatory disorder that may involve all the gastrointestinal tract with a prevalence of terminal ileum. Intestinal lesions have a characteristic discontinuous and segmental distribution and may affect all layers of the gut wall. Telocytes (TC), a peculi...

Descripción completa

Detalles Bibliográficos
Autores principales: Milia, Anna Franca, Ruffo, Martina, Manetti, Mirko, Rosa, Irene, Conte, Dalila, Fazi, Marilena, Messerini, Luca, Ibba-Manneschi, Lidia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons Ltd 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3914651/
https://www.ncbi.nlm.nih.gov/pubmed/24251911
http://dx.doi.org/10.1111/jcmm.12177
_version_ 1782302443985436672
author Milia, Anna Franca
Ruffo, Martina
Manetti, Mirko
Rosa, Irene
Conte, Dalila
Fazi, Marilena
Messerini, Luca
Ibba-Manneschi, Lidia
author_facet Milia, Anna Franca
Ruffo, Martina
Manetti, Mirko
Rosa, Irene
Conte, Dalila
Fazi, Marilena
Messerini, Luca
Ibba-Manneschi, Lidia
author_sort Milia, Anna Franca
collection PubMed
description Crohn’s disease (CD) is a relapsing chronic inflammatory disorder that may involve all the gastrointestinal tract with a prevalence of terminal ileum. Intestinal lesions have a characteristic discontinuous and segmental distribution and may affect all layers of the gut wall. Telocytes (TC), a peculiar type of stromal cells, have been recently identified in a variety of tissues and organs, including gastrointestinal tract of humans and mammals. Several roles have been proposed for TC, including mechanical support, spatial relationships with different cell types, intercellular signalling and modulation of intestinal motility. The aim of our study was to investigate the presence and distribution of TC in disease-affected and -unaffected ileal specimens from CD patients compared with controls. TC were identified by CD34/PDGFRα immunohistochemistry. In affected CD specimens TC disappeared, particularly where fibrosis and architectural derangement of the intestinal wall were observed. In the thickened muscularis mucosae and submucosa, few TC entrapped in the fibrotic extracellular matrix were found. A discontinuous network of TC was present around smooth muscle bundles, ganglia and enteric strands in the altered muscularis propria. At the myenteric plexus, the loss of TC network was paralleled by the loss of interstitial cells of Cajal network. In the unaffected CD specimens, TC were preserved in their distribution. Our results suggest that in CD the loss of TC might have important pathophysiological implications contributing to the architectural derangement of the intestinal wall and gut dysmotility. Further functional studies are necessary to better clarify the role of TC loss in CD pathophysiology.
format Online
Article
Text
id pubmed-3914651
institution National Center for Biotechnology Information
language English
publishDate 2013
publisher John Wiley & Sons Ltd
record_format MEDLINE/PubMed
spelling pubmed-39146512014-12-03 Telocytes in Crohn’s disease Milia, Anna Franca Ruffo, Martina Manetti, Mirko Rosa, Irene Conte, Dalila Fazi, Marilena Messerini, Luca Ibba-Manneschi, Lidia J Cell Mol Med Original Articles Crohn’s disease (CD) is a relapsing chronic inflammatory disorder that may involve all the gastrointestinal tract with a prevalence of terminal ileum. Intestinal lesions have a characteristic discontinuous and segmental distribution and may affect all layers of the gut wall. Telocytes (TC), a peculiar type of stromal cells, have been recently identified in a variety of tissues and organs, including gastrointestinal tract of humans and mammals. Several roles have been proposed for TC, including mechanical support, spatial relationships with different cell types, intercellular signalling and modulation of intestinal motility. The aim of our study was to investigate the presence and distribution of TC in disease-affected and -unaffected ileal specimens from CD patients compared with controls. TC were identified by CD34/PDGFRα immunohistochemistry. In affected CD specimens TC disappeared, particularly where fibrosis and architectural derangement of the intestinal wall were observed. In the thickened muscularis mucosae and submucosa, few TC entrapped in the fibrotic extracellular matrix were found. A discontinuous network of TC was present around smooth muscle bundles, ganglia and enteric strands in the altered muscularis propria. At the myenteric plexus, the loss of TC network was paralleled by the loss of interstitial cells of Cajal network. In the unaffected CD specimens, TC were preserved in their distribution. Our results suggest that in CD the loss of TC might have important pathophysiological implications contributing to the architectural derangement of the intestinal wall and gut dysmotility. Further functional studies are necessary to better clarify the role of TC loss in CD pathophysiology. John Wiley & Sons Ltd 2013-12 2013-11-19 /pmc/articles/PMC3914651/ /pubmed/24251911 http://dx.doi.org/10.1111/jcmm.12177 Text en © 2013 The Authors. Journal of Cellular and Molecular Medicine published by John Wiley & Sons Ltd and Foundation for Cellular and Molecular Medicine http://creativecommons.org/licenses/by/3.0/ This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Milia, Anna Franca
Ruffo, Martina
Manetti, Mirko
Rosa, Irene
Conte, Dalila
Fazi, Marilena
Messerini, Luca
Ibba-Manneschi, Lidia
Telocytes in Crohn’s disease
title Telocytes in Crohn’s disease
title_full Telocytes in Crohn’s disease
title_fullStr Telocytes in Crohn’s disease
title_full_unstemmed Telocytes in Crohn’s disease
title_short Telocytes in Crohn’s disease
title_sort telocytes in crohn’s disease
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3914651/
https://www.ncbi.nlm.nih.gov/pubmed/24251911
http://dx.doi.org/10.1111/jcmm.12177
work_keys_str_mv AT miliaannafranca telocytesincrohnsdisease
AT ruffomartina telocytesincrohnsdisease
AT manettimirko telocytesincrohnsdisease
AT rosairene telocytesincrohnsdisease
AT contedalila telocytesincrohnsdisease
AT fazimarilena telocytesincrohnsdisease
AT messeriniluca telocytesincrohnsdisease
AT ibbamanneschilidia telocytesincrohnsdisease