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Downregulation of ICCs and PDGFRα+ cells on colonic dysmotility in hirschsprung disease
BACKGROUND: To investigate the effect of the distribution and expression of interstitial cells of Cajal (ICCs) and platelet-derived growth factor receptor-α positive (PDGFRα+) cells in different colon segments on colonic motility in children with Hirschsprung disease (HSCR). METHODS: Smooth muscles...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9869412/ https://www.ncbi.nlm.nih.gov/pubmed/36699302 http://dx.doi.org/10.3389/fped.2022.975799 |
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author | Gu, Aiming Wu, Zhihao Wang, Peng Liu, Jun Wang, Jianfeng Wang, Qianqian Chen, Jie |
author_facet | Gu, Aiming Wu, Zhihao Wang, Peng Liu, Jun Wang, Jianfeng Wang, Qianqian Chen, Jie |
author_sort | Gu, Aiming |
collection | PubMed |
description | BACKGROUND: To investigate the effect of the distribution and expression of interstitial cells of Cajal (ICCs) and platelet-derived growth factor receptor-α positive (PDGFRα+) cells in different colon segments on colonic motility in children with Hirschsprung disease (HSCR). METHODS: Smooth muscles of the narrow and dilated segments of the colon were obtained from 16 pediatric patients with HSCR. The proximal margin was set as the control section. The mRNA and protein expressions of c-Kit, PDGFRα, ANO1, and SK3 channels were examined. Circular smooth muscle strips of the colon were prepared for performing electrophysiology experiments using electric field stimulation (EFS) and intervention from different drugs (TTX, NPPB, Apamin, L-NAME, and CyPPA). RESULTS: The mRNA and protein expressions of c-Kit, ANO1, PDGFRα, and SK3 were much lower in the narrow segment than those in the dilated and proximal segments of the colon. The narrow segment showed a considerably spontaneous contraction of the muscle strip. After the EFS, the relaxation response decreased from the proximal to the narrow segment, whereas the contraction response increased. TTX blocking did not cause any significant changes in the narrow segment. In contrast, when NPPB, Apamin, L-NAME, and CyPPA were used to intervene in the muscle strips, the proximal segment showed a more sensitive inhibitory or excitatory response than the narrow segment. CONCLUSIONS: Downregulation of the ICCs and PDGFRα+ cells from the proximal to narrow segment may be responsible for the dysmotility of the colon in pediatric HSCR. |
format | Online Article Text |
id | pubmed-9869412 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-98694122023-01-24 Downregulation of ICCs and PDGFRα+ cells on colonic dysmotility in hirschsprung disease Gu, Aiming Wu, Zhihao Wang, Peng Liu, Jun Wang, Jianfeng Wang, Qianqian Chen, Jie Front Pediatr Pediatrics BACKGROUND: To investigate the effect of the distribution and expression of interstitial cells of Cajal (ICCs) and platelet-derived growth factor receptor-α positive (PDGFRα+) cells in different colon segments on colonic motility in children with Hirschsprung disease (HSCR). METHODS: Smooth muscles of the narrow and dilated segments of the colon were obtained from 16 pediatric patients with HSCR. The proximal margin was set as the control section. The mRNA and protein expressions of c-Kit, PDGFRα, ANO1, and SK3 channels were examined. Circular smooth muscle strips of the colon were prepared for performing electrophysiology experiments using electric field stimulation (EFS) and intervention from different drugs (TTX, NPPB, Apamin, L-NAME, and CyPPA). RESULTS: The mRNA and protein expressions of c-Kit, ANO1, PDGFRα, and SK3 were much lower in the narrow segment than those in the dilated and proximal segments of the colon. The narrow segment showed a considerably spontaneous contraction of the muscle strip. After the EFS, the relaxation response decreased from the proximal to the narrow segment, whereas the contraction response increased. TTX blocking did not cause any significant changes in the narrow segment. In contrast, when NPPB, Apamin, L-NAME, and CyPPA were used to intervene in the muscle strips, the proximal segment showed a more sensitive inhibitory or excitatory response than the narrow segment. CONCLUSIONS: Downregulation of the ICCs and PDGFRα+ cells from the proximal to narrow segment may be responsible for the dysmotility of the colon in pediatric HSCR. Frontiers Media S.A. 2023-01-09 /pmc/articles/PMC9869412/ /pubmed/36699302 http://dx.doi.org/10.3389/fped.2022.975799 Text en © 2023 Gu, Wu, Wang, Liu, Wang, Wang and Chen. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY) (https://creativecommons.org/licenses/by/4.0/) . The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Pediatrics Gu, Aiming Wu, Zhihao Wang, Peng Liu, Jun Wang, Jianfeng Wang, Qianqian Chen, Jie Downregulation of ICCs and PDGFRα+ cells on colonic dysmotility in hirschsprung disease |
title | Downregulation of ICCs and PDGFRα+ cells on colonic dysmotility in hirschsprung disease |
title_full | Downregulation of ICCs and PDGFRα+ cells on colonic dysmotility in hirschsprung disease |
title_fullStr | Downregulation of ICCs and PDGFRα+ cells on colonic dysmotility in hirschsprung disease |
title_full_unstemmed | Downregulation of ICCs and PDGFRα+ cells on colonic dysmotility in hirschsprung disease |
title_short | Downregulation of ICCs and PDGFRα+ cells on colonic dysmotility in hirschsprung disease |
title_sort | downregulation of iccs and pdgfrα+ cells on colonic dysmotility in hirschsprung disease |
topic | Pediatrics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9869412/ https://www.ncbi.nlm.nih.gov/pubmed/36699302 http://dx.doi.org/10.3389/fped.2022.975799 |
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