Development of the aganglionic colon following surgical rescue in a cell therapy model of Hirschsprung disease in rat

• Published in: Disease models & mechanisms Vol. 16; no. 6
• Main Authors: Furness, John B, Lei, Enie, Hunne, Billie, Adams, Cameron D, Burns, Alan J, Wykosky, Jill, Fazio Coles, Therese E, Fothergill, Linda J, Molero, Juan C, Pustovit, Ruslan V, Stamp, Lincon A
• Format: Journal Article
• Language: English
• Published: England The Company of Biologists Ltd 01.06.2023; The Company of Biologists
• Subjects: Animals; Cell- and Tissue-Based Therapy; colon; Colon - pathology; enteric nervous system; enteric neurons; hirschsprung disease; Hirschsprung Disease - pathology; Hirschsprung Disease - therapy; intestinal bypass; Intestines - pathology; Neurons - pathology; Rats; stem cell therapy; Enteric nervous system; Colon; Stem cell therapy; Enteric neurons; Intestinal bypass; Hirschsprung disease
• ISSN: 1754-8403; 1754-8411
• DOI: 10.1242/dmm.050055

Patients with Hirschsprung disease lack enteric ganglia in the distal colon and propulsion of colorectal content is substantially impaired. Proposed stem cell therapies to replace neurons require surgical bypass of the aganglionic bowel during re-colonization, but there is inadequate knowledge of the consequences of bypass. We performed bypass surgery in Ednrb-/- Hirschsprung rat pups. Surgically rescued rats failed to thrive, an outcome reversed by supplying electrolyte- and glucose-enriched drinking water. Histologically, the bypassed colon had normal structure, but grew substantially less in diameter than the functional region proximal to the bypass. Extrinsic sympathetic and spinal afferent neurons projected to their normal targets, including arteries and the circular muscle, in aganglionic regions. However, although axons of intrinsic excitatory and inhibitory neurons grew into the aganglionic region, their normally dense innervation of circular muscle was not restored. Large nerve trunks that contained tyrosine hydroxylase (TH)-, calcitonin gene-related peptide (CGRP, encoded by Calca or Calcb)-, neuronal nitric oxide synthase (nNOS or NOS1)-, vasoactive intestinal peptide (VIP)- and tachykinin (encoded by Tac1)-immunoreactive axons occurred in the distal aganglionic region. We conclude that the rescued Ednrb-/- rat provides a good model for the development of cell therapies for the treatment of Hirschsprung disease.