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Morphology of the interstitial cells of Cajal of the human ileum from foetal to neonatal life

The so-called interstitial cells of Cajal myenteric plexus (ICC-MP), interstitial cells of Cajal intramuscular (ICC-IM) and interstitial cells of Cajal deep muscular plexus (ICC-DMP) are the three types of ICC endowed within the intestinal muscle coat where they play different roles in gut motility....

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Detalles Bibliográficos
Autores principales: Faussone-Pellegrini, Maria-Simonetta, Vannucchi, Maria-Giuliana, Alaggio, Rita, Strojna, Aleksandra, Midrio, Paola
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3922354/
https://www.ncbi.nlm.nih.gov/pubmed/17635640
http://dx.doi.org/10.1111/j.1582-4934.2007.00043.x
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author Faussone-Pellegrini, Maria-Simonetta
Vannucchi, Maria-Giuliana
Alaggio, Rita
Strojna, Aleksandra
Midrio, Paola
author_facet Faussone-Pellegrini, Maria-Simonetta
Vannucchi, Maria-Giuliana
Alaggio, Rita
Strojna, Aleksandra
Midrio, Paola
author_sort Faussone-Pellegrini, Maria-Simonetta
collection PubMed
description The so-called interstitial cells of Cajal myenteric plexus (ICC-MP), interstitial cells of Cajal intramuscular (ICC-IM) and interstitial cells of Cajal deep muscular plexus (ICC-DMP) are the three types of ICC endowed within the intestinal muscle coat where they play different roles in gut motility. Studies on ICC ontogenesis showed ICC-MP in the human ileum by 7–9 weeks while information on ICC-IM and ICC-DMP in foetuses and new-borns are not exhaustive. Functional recordings in the fasting state of prematurely born babies aged 28–37 weeks showed immature ileal motility. To gain more information on the time of appearance of the three ICC types in the human ileum and on the steps of the acquisition of mature features, we studied by c-kit immuno-histochemistry foetuses aged 17–27 weeks and newborns aged 36–41 weeks. In parallel, the maturative steps of enteric plexuses and muscle layers were immunohistochemically examined by using anti-neuron specific enolase (NSE), anti-S-100 and anti-α smooth muscle actin (αSMA) antibodies. The appearance and differentiation of all the ICC types were seen to occur in concomitance with those of the related nerve plexuses and muscle layers. ICC-MP appeared first, ICC-IM and ICC-DMP later and their differentiation was incomplete at birth. In conclusion, the ICC-MP, the intestinal pacemaker cells, in spite of absence of food intake, are already present during the foetal life and the ICC-IM appear by pre-term life, thus ensuring neurotransmission. The ICC-DMP and their related nerve plexus and smooth muscle cells, i.e. the intestinal stretch receptor, begin to differentiate at birth. These findings might help in predicting neonatal ileal motor behaviour and in interpreting the role of ICC abnormalities in the pathophysiology of intestinal motile disorders of neonates and young children.
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spelling pubmed-39223542015-04-27 Morphology of the interstitial cells of Cajal of the human ileum from foetal to neonatal life Faussone-Pellegrini, Maria-Simonetta Vannucchi, Maria-Giuliana Alaggio, Rita Strojna, Aleksandra Midrio, Paola J Cell Mol Med Articles The so-called interstitial cells of Cajal myenteric plexus (ICC-MP), interstitial cells of Cajal intramuscular (ICC-IM) and interstitial cells of Cajal deep muscular plexus (ICC-DMP) are the three types of ICC endowed within the intestinal muscle coat where they play different roles in gut motility. Studies on ICC ontogenesis showed ICC-MP in the human ileum by 7–9 weeks while information on ICC-IM and ICC-DMP in foetuses and new-borns are not exhaustive. Functional recordings in the fasting state of prematurely born babies aged 28–37 weeks showed immature ileal motility. To gain more information on the time of appearance of the three ICC types in the human ileum and on the steps of the acquisition of mature features, we studied by c-kit immuno-histochemistry foetuses aged 17–27 weeks and newborns aged 36–41 weeks. In parallel, the maturative steps of enteric plexuses and muscle layers were immunohistochemically examined by using anti-neuron specific enolase (NSE), anti-S-100 and anti-α smooth muscle actin (αSMA) antibodies. The appearance and differentiation of all the ICC types were seen to occur in concomitance with those of the related nerve plexuses and muscle layers. ICC-MP appeared first, ICC-IM and ICC-DMP later and their differentiation was incomplete at birth. In conclusion, the ICC-MP, the intestinal pacemaker cells, in spite of absence of food intake, are already present during the foetal life and the ICC-IM appear by pre-term life, thus ensuring neurotransmission. The ICC-DMP and their related nerve plexus and smooth muscle cells, i.e. the intestinal stretch receptor, begin to differentiate at birth. These findings might help in predicting neonatal ileal motor behaviour and in interpreting the role of ICC abnormalities in the pathophysiology of intestinal motile disorders of neonates and young children. Blackwell Publishing Ltd 2007-05 2007-06-14 /pmc/articles/PMC3922354/ /pubmed/17635640 http://dx.doi.org/10.1111/j.1582-4934.2007.00043.x Text en
spellingShingle Articles
Faussone-Pellegrini, Maria-Simonetta
Vannucchi, Maria-Giuliana
Alaggio, Rita
Strojna, Aleksandra
Midrio, Paola
Morphology of the interstitial cells of Cajal of the human ileum from foetal to neonatal life
title Morphology of the interstitial cells of Cajal of the human ileum from foetal to neonatal life
title_full Morphology of the interstitial cells of Cajal of the human ileum from foetal to neonatal life
title_fullStr Morphology of the interstitial cells of Cajal of the human ileum from foetal to neonatal life
title_full_unstemmed Morphology of the interstitial cells of Cajal of the human ileum from foetal to neonatal life
title_short Morphology of the interstitial cells of Cajal of the human ileum from foetal to neonatal life
title_sort morphology of the interstitial cells of cajal of the human ileum from foetal to neonatal life
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3922354/
https://www.ncbi.nlm.nih.gov/pubmed/17635640
http://dx.doi.org/10.1111/j.1582-4934.2007.00043.x
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