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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...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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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. |
format | Online Article Text |
id | pubmed-5890251 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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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