Enhanced enteric neurogenesis by Schwann cell precursors in mouse models of Hirschsprung disease

Glia ◽  
2021 ◽  
Author(s):  
Toshihiro Uesaka ◽  
Mitsumasa Okamoto ◽  
Mayumi Nagashimada ◽  
Yoshihiro Tsuda ◽  
Miho Kihara ◽  
...  
2017 ◽  
Vol 114 (45) ◽  
pp. 11980-11985 ◽  
Author(s):  
Isabel Espinosa-Medina ◽  
Ben Jevans ◽  
Franck Boismoreau ◽  
Zoubida Chettouh ◽  
Hideki Enomoto ◽  
...  

Most of the enteric nervous system derives from the “vagal” neural crest, lying at the level of somites 1–7, which invades the digestive tract rostro-caudally from the foregut to the hindgut. Little is known about the initial phase of this colonization, which brings enteric precursors into the foregut. Here we show that the “vagal crest” subsumes two populations of enteric precursors with contrasted origins, initial modes of migration, and destinations. Crest cells adjacent to somites 1 and 2 produce Schwann cell precursors that colonize the vagus nerve, which in turn guides them into the esophagus and stomach. Crest cells adjacent to somites 3–7 belong to the crest streams contributing to sympathetic chains: they migrate ventrally, seed the sympathetic chains, and colonize the entire digestive tract thence. Accordingly, enteric ganglia, like sympathetic ones, are atrophic when deprived of signaling through the tyrosine kinase receptor ErbB3, while half of the esophageal ganglia require, like parasympathetic ones, the nerve-associated form of the ErbB3 ligand, Neuregulin-1. These dependencies might bear relevance to Hirschsprung disease, with which alleles of Neuregulin-1 are associated.


Author(s):  
Marketa Kaucka ◽  
Bara Szarowska ◽  
Michaela Kavkova ◽  
Maria Eleni Kastriti ◽  
Polina Kameneva ◽  
...  

AbstractMelanocytes are pigmented cells residing mostly in the skin and hair follicles of vertebrates, where they contribute to colouration and protection against UV-B radiation. However, the spectrum of their functions reaches far beyond that. For instance, these pigment-producing cells are found inside the inner ear, where they contribute to the hearing function, and in the heart, where they are involved in the electrical conductivity and support the stiffness of cardiac valves. The embryonic origin of such extracutaneous melanocytes is not clear. We took advantage of lineage-tracing experiments combined with 3D visualizations and gene knockout strategies to address this long-standing question. We revealed that Schwann cell precursors are recruited from the local innervation during embryonic development and give rise to extracutaneous melanocytes in the heart, brain meninges, inner ear, and other locations. In embryos with a knockout of the EdnrB receptor, a condition imitating Waardenburg syndrome, we observed only nerve-associated melanoblasts, which failed to detach from the nerves and to enter the inner ear. Finally, we looked into the evolutionary aspects of extracutaneous melanocytes and found that pigment cells are associated mainly with nerves and blood vessels in amphibians and fish. This new knowledge of the nerve-dependent origin of extracutaneous pigment cells might be directly relevant to the formation of extracutaneous melanoma in humans.


Author(s):  
Dmitrii Kamenev ◽  
Kazunori Sunadome ◽  
Maxim Shirokov ◽  
Andrey S. Chagin ◽  
Ajeet Singh ◽  
...  

Glia ◽  
1991 ◽  
Vol 4 (2) ◽  
pp. 185-194 ◽  
Author(s):  
Kristjan R. Jessen ◽  
Rhona Mirsky

2020 ◽  
Vol 11 (1) ◽  
Author(s):  
Han-Seop Kim ◽  
Jae Yun Kim ◽  
Cho Lok Song ◽  
Ji Eun Jeong ◽  
Yee Sook Cho

2016 ◽  
Vol 19 (4) ◽  
pp. 433-448 ◽  
Author(s):  
Adam P.W. Johnston ◽  
Scott A. Yuzwa ◽  
Matthew J. Carr ◽  
Neemat Mahmud ◽  
Mekayla A. Storer ◽  
...  

Glia ◽  
2017 ◽  
Vol 66 (3) ◽  
pp. 465-476 ◽  
Author(s):  
Jorge B. Aquino ◽  
Romina Sierra

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