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Updated: Mar 31, 2026

Diagnosis of Hirschsprung's Disease by Immunostaining Rectal Suction Biopsies for Calretinin, S100 Protein and Protein Gene Product 9.5
Published on: April 26, 2019
Reduced expression of voltage-gated Kv11.1 (hERG) K(+) channels in aganglionic colon in Hirschsprung's disease
Christian Tomuschat1, Anne Marie O'Donnell1, David Coyle1
1National Children's Research Centre, Our Lady's Children's Hospital, Crumlin, Dublin 12, Ireland.
Insights
Decreased expression of Kv11.1 (hERG) channels in the aganglionic colon may cause increased bowel tone in Hirschsprung
Area of Science:
- Gastroenterology
- Molecular Biology
- Physiology
Background:
- Hirschsprung's disease (HSCR) pathophysiology, specifically the contracted aganglionic bowel segment, remains unclear.
- Kv11.1 (hERG) channels are crucial for smooth muscle function and membrane potential regulation.
Purpose of the Study:
- To investigate the expression and distribution of hERG channels in normal and HSCR patient colons.
- To explore the potential role of hERG channels in HSCR.
Main Methods:
- Compared hERG protein expression in ganglionic and aganglionic regions of HSCR patients (n=10) and controls (n=10).
- Utilized immunofluorescence, confocal microscopy, real-time PCR, and western blot analysis to quantify gene and protein expression.
Main Results:
- Normal colon showed strong hERG expression in interstitial cells of Cajal, PDGFRα(+) cells, and enteric neurons.
- Aganglionic HSCR bowel exhibited significantly decreased hERG gene and protein expression compared to controls.
Conclusions:
- This study is the first to demonstrate hERG channel expression in the human colon.
- Reduced hERG expression in the aganglionic colon may contribute to the increased tone observed in HSCR.
Purpose:
The pathophysiology of Hirschsprung's disease (HSCR) is not entirely understood. There is no clear explanation for the occurrence of the spastic or tonically contracted aganglionic segment of bowel. Kv11.1 (hERG) channels play a critical role in the regulation of the resting membrane potential as well as affecting either the force or frequency of contraction of smooth muscles. We designed this study to investigate the expression and distribution of hERG channels in the normal colon and the colon of patients with HSCR.
Methods:
We investigated hERG protein expression in both the ganglionic and aganglionic regions of HSCR patients (n = 10) versus normal control colon (n = 10). Protein distribution was assessed using immunofluorescence and confocal microscopy. Gene and protein expressions were quantified using real-time polymerase chain reaction, western blot analysis and densitometry.
Results:
Confocal microscopy of the normal colon revealed strong hERG channel expression in interstitial cells of Cajal, platelet-derived growth factor-alpha receptor- (PDGFRα(+)) positive cells and enteric neurons. hERG expression was markedly decreased in aganglionic bowel, whereas colonic hERG gene expression levels were significantly decreased in aganglionic compared to ganglionic bowel and controls (p < 0.05). Western blotting revealed decreased colonic hERG protein expression in aganglionic HSCR specimens compared to controls.
Conclusions:
We demonstrate, for the first time, the expression and distribution of hERG channels in the human colon. The decreased expression of hERG in the aganglionic colon may be responsible for the increased tone in the aganglionic narrow spastic segment of bowel.
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