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Contraction of basal filopodia controls periodic feather branching via Notch and FGF signaling

Branching morphogenesis is a general mechanism that increases the surface area of an organ. In chicken feathers, the flat epithelial sheath at the base of the follicle is transformed into periodic branches. How exactly the keratinocytes are organized into this pattern remains unclear. Here we show t...

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Autores principales: Cheng, Dongyang, Yan, Xiaoli, Qiu, Guofu, Zhang, Juan, Wang, Hanwei, Feng, Tingting, Tian, Yarong, Xu, Haiping, Wang, Meiqing, He, Wanzhong, Wu, Ping, Widelitz, Randall B, Chuong, Cheng-Ming, Yue, Zhicao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5890251/
https://www.ncbi.nlm.nih.gov/pubmed/29632339
http://dx.doi.org/10.1038/s41467-018-03801-z
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author Cheng, Dongyang
Yan, Xiaoli
Qiu, Guofu
Zhang, Juan
Wang, Hanwei
Feng, Tingting
Tian, Yarong
Xu, Haiping
Wang, Meiqing
He, Wanzhong
Wu, Ping
Widelitz, Randall B
Chuong, Cheng-Ming
Yue, Zhicao
author_facet Cheng, Dongyang
Yan, Xiaoli
Qiu, Guofu
Zhang, Juan
Wang, Hanwei
Feng, Tingting
Tian, Yarong
Xu, Haiping
Wang, Meiqing
He, Wanzhong
Wu, Ping
Widelitz, Randall B
Chuong, Cheng-Ming
Yue, Zhicao
author_sort Cheng, Dongyang
collection PubMed
description Branching morphogenesis is a general mechanism that increases the surface area of an organ. In chicken feathers, the flat epithelial sheath at the base of the follicle is transformed into periodic branches. How exactly the keratinocytes are organized into this pattern remains unclear. Here we show that in the feather follicle, the pre-branch basal keratinocytes have extensive filopodia, which contract and smooth out after branching. Manipulating the filopodia via small GTPases RhoA/Cdc42 also regulates branch formation. These basal filopodia help interpret the proximal-distal FGF gradient in the follicle. Furthermore, the topological arrangement of cell adhesion via E-Cadherin re-distribution controls the branching process. Periodic activation of Notch signaling drives the differential cell adhesion and contraction of basal filopodia, which occurs only below an FGF signaling threshold. Our results suggest a coordinated adjustment of cell shape and adhesion orchestrates feather branching, which is regulated by Notch and FGF signaling.
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spelling pubmed-58902512018-04-11 Contraction of basal filopodia controls periodic feather branching via Notch and FGF signaling Cheng, Dongyang Yan, Xiaoli Qiu, Guofu Zhang, Juan Wang, Hanwei Feng, Tingting Tian, Yarong Xu, Haiping Wang, Meiqing He, Wanzhong Wu, Ping Widelitz, Randall B Chuong, Cheng-Ming Yue, Zhicao Nat Commun Article Branching morphogenesis is a general mechanism that increases the surface area of an organ. In chicken feathers, the flat epithelial sheath at the base of the follicle is transformed into periodic branches. How exactly the keratinocytes are organized into this pattern remains unclear. Here we show that in the feather follicle, the pre-branch basal keratinocytes have extensive filopodia, which contract and smooth out after branching. Manipulating the filopodia via small GTPases RhoA/Cdc42 also regulates branch formation. These basal filopodia help interpret the proximal-distal FGF gradient in the follicle. Furthermore, the topological arrangement of cell adhesion via E-Cadherin re-distribution controls the branching process. Periodic activation of Notch signaling drives the differential cell adhesion and contraction of basal filopodia, which occurs only below an FGF signaling threshold. Our results suggest a coordinated adjustment of cell shape and adhesion orchestrates feather branching, which is regulated by Notch and FGF signaling. Nature Publishing Group UK 2018-04-09 /pmc/articles/PMC5890251/ /pubmed/29632339 http://dx.doi.org/10.1038/s41467-018-03801-z Text en © The Author(s) 2018 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/.
spellingShingle Article
Cheng, Dongyang
Yan, Xiaoli
Qiu, Guofu
Zhang, Juan
Wang, Hanwei
Feng, Tingting
Tian, Yarong
Xu, Haiping
Wang, Meiqing
He, Wanzhong
Wu, Ping
Widelitz, Randall B
Chuong, Cheng-Ming
Yue, Zhicao
Contraction of basal filopodia controls periodic feather branching via Notch and FGF signaling
title Contraction of basal filopodia controls periodic feather branching via Notch and FGF signaling
title_full Contraction of basal filopodia controls periodic feather branching via Notch and FGF signaling
title_fullStr Contraction of basal filopodia controls periodic feather branching via Notch and FGF signaling
title_full_unstemmed Contraction of basal filopodia controls periodic feather branching via Notch and FGF signaling
title_short Contraction of basal filopodia controls periodic feather branching via Notch and FGF signaling
title_sort contraction of basal filopodia controls periodic feather branching via notch and fgf signaling
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5890251/
https://www.ncbi.nlm.nih.gov/pubmed/29632339
http://dx.doi.org/10.1038/s41467-018-03801-z
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