Multipotent peripheral glial cells generate neuroendocrine cells of the adrenal medulla

Alessandro Furlan(Karolinska Institutet), Vyacheslav Dyachuk(ITMO University), Maria Eleni Kastriti(Karolinska Institutet), Laura Calvo-Enrique(Karolinska Institutet), Hind Abdo(Karolinska Institutet), Saïda Hadjab(Karolinska Institutet), Tatiana Chontorotzea(Karolinska Institutet), Natalia Akkuratova(Skolkovo Institute of Science and Technology), Dmitry Usoskin(Karolinska Institutet), Dmitrii Kamenev(Karolinska Institutet), Julian Petersen(Karolinska Institutet), Kazunori Sunadome(Karolinska Institutet), Fatima Memic(Karolinska Institutet), Ulrika Marklund(Karolinska Institutet), Kaj Fried(Karolinska Institutet), Piotr Topilko(Centre National de la Recherche Scientifique), François Lallemend(Karolinska Institutet), Peter V. Kharchenko(Harvard University), Patrik Ernfors(Karolinska Institutet), Igor Adameyko(Karolinska Institutet)
Science
July 7, 2017
Cited by 356Open Access
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Abstract

Adrenaline is a fundamental circulating hormone for bodily responses to internal and external stressors. Chromaffin cells of the adrenal medulla (AM) represent the main neuroendocrine adrenergic component and are believed to differentiate from neural crest cells. We demonstrate that large numbers of chromaffin cells arise from peripheral glial stem cells, termed Schwann cell precursors (SCPs). SCPs migrate along the visceral motor nerve to the vicinity of the forming adrenal gland, where they detach from the nerve and form postsynaptic neuroendocrine chromaffin cells. An intricate molecular logic drives two sequential phases of gene expression, one unique for a distinct transient cellular state and another for cell type specification. Subsequently, these programs down-regulate SCP-gene and up-regulate chromaffin cell-gene networks. The AM forms through limited cell expansion and requires the recruitment of numerous SCPs. Thus, peripheral nerves serve as a stem cell niche for neuroendocrine system development.


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