Three- and four-dimensional analysis of altered behavior of enteric neural crest derived cells in the Hirschsprung’s disease mouse model

2015 ◽  
Vol 32 (1) ◽  
pp. 3-7 ◽  
Author(s):  
Nana Nakazawa-Tanaka ◽  
Katsumi Miyahara ◽  
Naho Fujiwara ◽  
Masahiko Urao ◽  
Chihiro Akazawa ◽  
...  
Keyword(s):  
Mouse Model ◽  
Neural Crest ◽  
Dimensional Analysis ◽  
Hirschsprung's Disease ◽  
Hirschsprung’S Disease

The effect of laminin-1 on enteric neural crest-derived cell migration in the Hirschsprung’s disease mouse model

2017 ◽  
Vol 34 (2) ◽  
pp. 143-147 ◽  
Author(s):  
Nana Nakazawa-Tanaka ◽  
N. Fujiwara ◽  
K. Miyahara ◽  
S. Nakada ◽  
E. Arikawa-Hirasawa ◽  
...  
Keyword(s):  
Cell Migration ◽  
Mouse Model ◽  
Neural Crest ◽  
Hirschsprung's Disease ◽  
Hirschsprung’S Disease ◽  
Laminin 1

Altered differentiation of enteric neural crest-derived cells from endothelin receptor-B null mouse model of Hirschsprung’s disease

2016 ◽  
Vol 32 (12) ◽  
pp. 1095-1101 ◽  
Author(s):  
Naho Fujiwara ◽  
Katsumi Miyahara ◽  
Nana Nakazawa-Tanaka ◽  
Chihiro Akazawa ◽  
Atsuyuki Yamataka
Keyword(s):  
Mouse Model ◽  
Neural Crest ◽  
Hirschsprung's Disease ◽  
Hirschsprung’S Disease ◽  
Null Mouse ◽  
Endothelin Receptor ◽  
Endothelin Receptor B

Innervation of the entire internal anal sphincter in a mouse model of Hirschsprung’s disease: a first report

2018 ◽  
Vol 35 (2) ◽  
pp. 209-214 ◽  
Author(s):  
Masahiro Takeda ◽  
Katsumi Miyahara ◽  
Ryo Sueyoshi ◽  
Atsushi Arakawa ◽  
Geoffrey J. Lane ◽  
...  
Keyword(s):  
Mouse Model ◽  
Anal Sphincter ◽  
Internal Anal Sphincter ◽  
Hirschsprung's Disease ◽  
Hirschsprung’S Disease ◽  
First Report

scholarly journals Muscarinic cholinergic receptors in the piebald mouse model for Hirschsprung's disease

1983 ◽  
Vol 85 (2) ◽  
pp. 335-338 ◽  
Author(s):  
Edward R. Seidel ◽  
Jack Woods ◽  
Barbara E. Eikenburg ◽  
Leonard R. Johnson
Keyword(s):  
Mouse Model ◽  
Hirschsprung's Disease ◽  
Hirschsprung’S Disease ◽  
Cholinergic Receptors ◽  
Muscarinic Cholinergic Receptors ◽  
Muscarinic Cholinergic

scholarly journals Hirschsprung’s Disease—Recent Understanding of Embryonic Aspects, Etiopathogenesis and Future Treatment Avenues

Medicina ◽  
2020 ◽  
Vol 56 (11) ◽  
pp. 611 ◽  
Author(s):  
Martin Klein ◽  
Ivan Varga
Keyword(s):  
Neural Crest ◽  
Interstitial Cells Of Cajal ◽  
Hirschsprung's Disease ◽  
Hirschsprung’S Disease ◽  
Clinical Signs ◽  
Review Article ◽  
Live Births ◽  
Cell Based Therapy ◽  
Cells Of Cajal ◽  
Patients Experience

Hirschsprung’s disease is a neurocristopathy, caused by defective migration, proliferation, differentiation and survival of neural crest cells, leading to gut aganglionosis. It usually manifests rapidly after birth, affecting 1 in 5000 live births around the globe. In recent decades, there has been a significant improvement in the understanding of its genetics and the association with other congenital anomalies, which share the pathomechanism of improper development of the neural crest. Apart from that, several cell populations which do not originate from the neural crest, but contribute to the development of Hirschsprung’s disease, have also been described, namely mast cells and interstitial cells of Cajal. From the diagnostic perspective, researchers also focused on “Variants of Hirschsprung’s disease”, which can mimic the clinical signs of the disease, but are in fact different entities, with distinct prognosis and treatment approaches. The treatment of Hirschsprung’s disease is usually surgical resection of the aganglionic part of the intestine, however, as many as 30–50% of patients experience persisting symptoms. Considering this fact, this review article also outlines future hopes and perspectives in Hirschsprung’s disease management, which has the potential to benefit from the advancements in the fields of cell-based therapy and tissue engineering.

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