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Hypothalamic Rax(+) tanycytes contribute to tissue repair and tumorigenesis upon oncogene activation in mice

Hypothalamic tanycytes in median eminence (ME) are emerging as a crucial cell population that regulates endocrine output, energy balance and the diffusion of blood-born molecules. Tanycytes have recently been considered as potential somatic stem cells in the adult mammalian brain, but their regenera...

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Autores principales: Mu, Wenhui, Li, Si, Xu, Jingkai, Guo, Xize, Wu, Haoda, Chen, Zhenhua, Qiao, Lianyong, Helfer, Gisela, Lu, Falong, Liu, Chong, Wu, Qing-Feng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8052410/
https://www.ncbi.nlm.nih.gov/pubmed/33863883
http://dx.doi.org/10.1038/s41467-021-22640-z
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author Mu, Wenhui
Li, Si
Xu, Jingkai
Guo, Xize
Wu, Haoda
Chen, Zhenhua
Qiao, Lianyong
Helfer, Gisela
Lu, Falong
Liu, Chong
Wu, Qing-Feng
author_facet Mu, Wenhui
Li, Si
Xu, Jingkai
Guo, Xize
Wu, Haoda
Chen, Zhenhua
Qiao, Lianyong
Helfer, Gisela
Lu, Falong
Liu, Chong
Wu, Qing-Feng
author_sort Mu, Wenhui
collection PubMed
description Hypothalamic tanycytes in median eminence (ME) are emerging as a crucial cell population that regulates endocrine output, energy balance and the diffusion of blood-born molecules. Tanycytes have recently been considered as potential somatic stem cells in the adult mammalian brain, but their regenerative and tumorigenic capacities are largely unknown. Here we found that Rax+ tanycytes in ME of mice are largely quiescent but quickly enter the cell cycle upon neural injury for self-renewal and regeneration. Mechanistically, Igf1r signaling in tanycytes is required for tissue repair under injury conditions. Furthermore, Braf oncogenic activation is sufficient to transform Rax+ tanycytes into actively dividing tumor cells that eventually develop into a papillary craniopharyngioma-like tumor. Together, these findings uncover the regenerative and tumorigenic potential of tanycytes. Our study offers insights into the properties of tanycytes, which may help to manipulate tanycyte biology for regulating hypothalamic function and investigate the pathogenesis of clinically relevant tumors.
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spelling pubmed-80524102021-05-11 Hypothalamic Rax(+) tanycytes contribute to tissue repair and tumorigenesis upon oncogene activation in mice Mu, Wenhui Li, Si Xu, Jingkai Guo, Xize Wu, Haoda Chen, Zhenhua Qiao, Lianyong Helfer, Gisela Lu, Falong Liu, Chong Wu, Qing-Feng Nat Commun Article Hypothalamic tanycytes in median eminence (ME) are emerging as a crucial cell population that regulates endocrine output, energy balance and the diffusion of blood-born molecules. Tanycytes have recently been considered as potential somatic stem cells in the adult mammalian brain, but their regenerative and tumorigenic capacities are largely unknown. Here we found that Rax+ tanycytes in ME of mice are largely quiescent but quickly enter the cell cycle upon neural injury for self-renewal and regeneration. Mechanistically, Igf1r signaling in tanycytes is required for tissue repair under injury conditions. Furthermore, Braf oncogenic activation is sufficient to transform Rax+ tanycytes into actively dividing tumor cells that eventually develop into a papillary craniopharyngioma-like tumor. Together, these findings uncover the regenerative and tumorigenic potential of tanycytes. Our study offers insights into the properties of tanycytes, which may help to manipulate tanycyte biology for regulating hypothalamic function and investigate the pathogenesis of clinically relevant tumors. Nature Publishing Group UK 2021-04-16 /pmc/articles/PMC8052410/ /pubmed/33863883 http://dx.doi.org/10.1038/s41467-021-22640-z Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Mu, Wenhui
Li, Si
Xu, Jingkai
Guo, Xize
Wu, Haoda
Chen, Zhenhua
Qiao, Lianyong
Helfer, Gisela
Lu, Falong
Liu, Chong
Wu, Qing-Feng
Hypothalamic Rax(+) tanycytes contribute to tissue repair and tumorigenesis upon oncogene activation in mice
title Hypothalamic Rax(+) tanycytes contribute to tissue repair and tumorigenesis upon oncogene activation in mice
title_full Hypothalamic Rax(+) tanycytes contribute to tissue repair and tumorigenesis upon oncogene activation in mice
title_fullStr Hypothalamic Rax(+) tanycytes contribute to tissue repair and tumorigenesis upon oncogene activation in mice
title_full_unstemmed Hypothalamic Rax(+) tanycytes contribute to tissue repair and tumorigenesis upon oncogene activation in mice
title_short Hypothalamic Rax(+) tanycytes contribute to tissue repair and tumorigenesis upon oncogene activation in mice
title_sort hypothalamic rax(+) tanycytes contribute to tissue repair and tumorigenesis upon oncogene activation in mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8052410/
https://www.ncbi.nlm.nih.gov/pubmed/33863883
http://dx.doi.org/10.1038/s41467-021-22640-z
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