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Delayed development of interstitial cells of Cajal in the ileum of a human case of gastroschisis

The Interstitial Cells of Cajal (ICC) are responsible for rhythmic electrical activity. A paralytic ileus is present in gastroschisis (GS), a malformation due to a defective closure of the abdominal wall through which part of the intestine herniates during pregnancy. In experimental GS, ICC morpholo...

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Autores principales: Midrio, Paola, Vannucchi, Maria Giuliana, Pieri, Laura, Alaggio, Rita, Faussone-Pellegrini, Maria Simonetta
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3822536/
https://www.ncbi.nlm.nih.gov/pubmed/18266958
http://dx.doi.org/10.1111/j.1582-4934.2008.00277.x
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author Midrio, Paola
Vannucchi, Maria Giuliana
Pieri, Laura
Alaggio, Rita
Faussone-Pellegrini, Maria Simonetta
author_facet Midrio, Paola
Vannucchi, Maria Giuliana
Pieri, Laura
Alaggio, Rita
Faussone-Pellegrini, Maria Simonetta
author_sort Midrio, Paola
collection PubMed
description The Interstitial Cells of Cajal (ICC) are responsible for rhythmic electrical activity. A paralytic ileus is present in gastroschisis (GS), a malformation due to a defective closure of the abdominal wall through which part of the intestine herniates during pregnancy. In experimental GS, ICC morphological immaturity was shown in the rat foetus at-term but it could not be demonstrated whether differentiation is accomplished post-natally. For this purpose we morphologically investigated ICC, as well as enteric neurons and smooth muscle cells, in a case of human GS at birth and 1 month later when peristaltic activity had initiated. A 36 weeks gestation female was born by c/section with prenatal diagnosis of GS and possible volvulus of the herniated intestine. At birth, the necrotic intestine was resected and both ileostomy and colostomy were performed. The intestine continuity was restored after 4 weeks. Intestinal specimens, taken during both operations at the level of the proximal stoma, were immunostained with c-kit, neuron-specific-enolase and α-smooth-muscle-actin antibodies and some processed for electron microscopy. ICC were present at the myenteric plexus only. At birth, these cells were rare and ultrastructurally immature; 1 month later, when partial enteral feeding was tolerated, they formed rows or groups and many of them were ultrastructurally differentiated. Neurons and smooth muscle cells, immature at birth, had developed after 1 month. Therefore, ICC differentiation, as well as that of neurons and smooth muscle cells, is delayed at birth and this might explain the paralytic ileus in GS. One month later, differentiation quickly proceeded at all cellular levels paralleling the increasing tolerance of enteral nutrition.
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spelling pubmed-38225362015-04-27 Delayed development of interstitial cells of Cajal in the ileum of a human case of gastroschisis Midrio, Paola Vannucchi, Maria Giuliana Pieri, Laura Alaggio, Rita Faussone-Pellegrini, Maria Simonetta J Cell Mol Med Articles The Interstitial Cells of Cajal (ICC) are responsible for rhythmic electrical activity. A paralytic ileus is present in gastroschisis (GS), a malformation due to a defective closure of the abdominal wall through which part of the intestine herniates during pregnancy. In experimental GS, ICC morphological immaturity was shown in the rat foetus at-term but it could not be demonstrated whether differentiation is accomplished post-natally. For this purpose we morphologically investigated ICC, as well as enteric neurons and smooth muscle cells, in a case of human GS at birth and 1 month later when peristaltic activity had initiated. A 36 weeks gestation female was born by c/section with prenatal diagnosis of GS and possible volvulus of the herniated intestine. At birth, the necrotic intestine was resected and both ileostomy and colostomy were performed. The intestine continuity was restored after 4 weeks. Intestinal specimens, taken during both operations at the level of the proximal stoma, were immunostained with c-kit, neuron-specific-enolase and α-smooth-muscle-actin antibodies and some processed for electron microscopy. ICC were present at the myenteric plexus only. At birth, these cells were rare and ultrastructurally immature; 1 month later, when partial enteral feeding was tolerated, they formed rows or groups and many of them were ultrastructurally differentiated. Neurons and smooth muscle cells, immature at birth, had developed after 1 month. Therefore, ICC differentiation, as well as that of neurons and smooth muscle cells, is delayed at birth and this might explain the paralytic ileus in GS. One month later, differentiation quickly proceeded at all cellular levels paralleling the increasing tolerance of enteral nutrition. Blackwell Publishing Ltd 2008-04 2008-02-08 /pmc/articles/PMC3822536/ /pubmed/18266958 http://dx.doi.org/10.1111/j.1582-4934.2008.00277.x Text en ©2008 The Authors Journal compilation © 2008 Foundation for Cellular and Molecular Medicine/Blackwell Publishing Ltd
spellingShingle Articles
Midrio, Paola
Vannucchi, Maria Giuliana
Pieri, Laura
Alaggio, Rita
Faussone-Pellegrini, Maria Simonetta
Delayed development of interstitial cells of Cajal in the ileum of a human case of gastroschisis
title Delayed development of interstitial cells of Cajal in the ileum of a human case of gastroschisis
title_full Delayed development of interstitial cells of Cajal in the ileum of a human case of gastroschisis
title_fullStr Delayed development of interstitial cells of Cajal in the ileum of a human case of gastroschisis
title_full_unstemmed Delayed development of interstitial cells of Cajal in the ileum of a human case of gastroschisis
title_short Delayed development of interstitial cells of Cajal in the ileum of a human case of gastroschisis
title_sort delayed development of interstitial cells of cajal in the ileum of a human case of gastroschisis
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3822536/
https://www.ncbi.nlm.nih.gov/pubmed/18266958
http://dx.doi.org/10.1111/j.1582-4934.2008.00277.x
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