@article{2333fc4d669d445d816ef313a2227623,
title = "A pre-vertebrate endodermal origin of calcitonin-producing neuroendocrine cells",
abstract = "Vertebrate calcitonin-producing cells (C-cells) are neuroendocrine cells that secrete the small peptide hormone calcitonin in response to elevated blood calcium levels. Whereas mouse C-cells reside within the thyroid gland and derive from pharyngeal endoderm, avian C-cells are located within ultimobranchial glands and have been reported to derive from the neural crest. We use a comparative cell lineage tracing approach in a range of vertebrate model systems to resolve the ancestral embryonic origin of vertebrate C-cells. We find, contrary to previous studies, that chick C-cells derive from pharyngeal endoderm, with neural crest-derived cells instead contributing to connective tissue intimately associated with C-cells in the ultimobranchial gland. This endodermal origin of C-cells is conserved in a ray-finned bony fish (zebrafish) and a cartilaginous fish (the little skate, Leucoraja erinacea). Furthermore, we discover putative C-cell homologs within the endodermally-derived pharyngeal epithelium of the ascidian Ciona intestinalis and the amphioxus Branchiostoma lanceolatum, two invertebrate chordates that lack neural crest cells. Our findings point to a conserved endodermal origin of C-cells across vertebrates and to a pre-vertebrate origin of this cell type along the chordate stem.",
keywords = "calcitonin, endoderm, evolution, neural crest, neuroendocrine",
author = "Rees, \{Jenaid M.\} and Katie Kirk and Giacomo Gattoni and Dorit Hockman and Victoria Sleight and Ritter, \{Dylan J.\} and {\`E}lia Benito-Gutierrez and Knapik, \{Ela W.\} and Crump, \{J. Gage\} and Peter Fabian and Gillis, \{J Andrew\}",
year = "2024",
month = oct,
doi = "10.1242/dev.202821",
language = "English",
volume = "151",
journal = "Development",
issn = "0950-1991",
publisher = "Company of Biologists Ltd",
number = "20",
}