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Mapping the molecular and structural specialization of the skin basement membrane for inter-tissue interactions

Inter-tissue interaction is fundamental to multicellularity. Although the basement membrane (BM) is located at tissue interfaces, its mode of action in inter-tissue interactions remains poorly understood, mainly because the molecular and structural details of the BM at distinct inter-tissue interfac...

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Autores principales: Tsutsui, Ko, Machida, Hiroki, Nakagawa, Asako, Ahn, Kyungmin, Morita, Ritsuko, Sekiguchi, Kiyotoshi, Miner, Jeffrey H., Fujiwara, Hironobu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8110968/
https://www.ncbi.nlm.nih.gov/pubmed/33972551
http://dx.doi.org/10.1038/s41467-021-22881-y
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author Tsutsui, Ko
Machida, Hiroki
Nakagawa, Asako
Ahn, Kyungmin
Morita, Ritsuko
Sekiguchi, Kiyotoshi
Miner, Jeffrey H.
Fujiwara, Hironobu
author_facet Tsutsui, Ko
Machida, Hiroki
Nakagawa, Asako
Ahn, Kyungmin
Morita, Ritsuko
Sekiguchi, Kiyotoshi
Miner, Jeffrey H.
Fujiwara, Hironobu
author_sort Tsutsui, Ko
collection PubMed
description Inter-tissue interaction is fundamental to multicellularity. Although the basement membrane (BM) is located at tissue interfaces, its mode of action in inter-tissue interactions remains poorly understood, mainly because the molecular and structural details of the BM at distinct inter-tissue interfaces remain unclear. By combining quantitative transcriptomics and immunohistochemistry, we systematically identify the cellular origin, molecular identity and tissue distribution of extracellular matrix molecules in mouse hair follicles, and reveal that BM composition and architecture are exquisitely specialized for distinct inter-tissue interactions, including epithelial–fibroblast, epithelial–muscle and epithelial–nerve interactions. The epithelial–fibroblast interface, namely, hair germ–dermal papilla interface, makes asymmetrically organized side-specific heterogeneity in the BM, defined by the newly characterized interface, hook and mesh BMs. One component of these BMs, laminin α5, is required for hair cycle regulation and hair germ–dermal papilla anchoring. Our study highlights the significance of BM heterogeneity in distinct inter-tissue interactions.
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spelling pubmed-81109682021-05-14 Mapping the molecular and structural specialization of the skin basement membrane for inter-tissue interactions Tsutsui, Ko Machida, Hiroki Nakagawa, Asako Ahn, Kyungmin Morita, Ritsuko Sekiguchi, Kiyotoshi Miner, Jeffrey H. Fujiwara, Hironobu Nat Commun Article Inter-tissue interaction is fundamental to multicellularity. Although the basement membrane (BM) is located at tissue interfaces, its mode of action in inter-tissue interactions remains poorly understood, mainly because the molecular and structural details of the BM at distinct inter-tissue interfaces remain unclear. By combining quantitative transcriptomics and immunohistochemistry, we systematically identify the cellular origin, molecular identity and tissue distribution of extracellular matrix molecules in mouse hair follicles, and reveal that BM composition and architecture are exquisitely specialized for distinct inter-tissue interactions, including epithelial–fibroblast, epithelial–muscle and epithelial–nerve interactions. The epithelial–fibroblast interface, namely, hair germ–dermal papilla interface, makes asymmetrically organized side-specific heterogeneity in the BM, defined by the newly characterized interface, hook and mesh BMs. One component of these BMs, laminin α5, is required for hair cycle regulation and hair germ–dermal papilla anchoring. Our study highlights the significance of BM heterogeneity in distinct inter-tissue interactions. Nature Publishing Group UK 2021-05-10 /pmc/articles/PMC8110968/ /pubmed/33972551 http://dx.doi.org/10.1038/s41467-021-22881-y 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
Tsutsui, Ko
Machida, Hiroki
Nakagawa, Asako
Ahn, Kyungmin
Morita, Ritsuko
Sekiguchi, Kiyotoshi
Miner, Jeffrey H.
Fujiwara, Hironobu
Mapping the molecular and structural specialization of the skin basement membrane for inter-tissue interactions
title Mapping the molecular and structural specialization of the skin basement membrane for inter-tissue interactions
title_full Mapping the molecular and structural specialization of the skin basement membrane for inter-tissue interactions
title_fullStr Mapping the molecular and structural specialization of the skin basement membrane for inter-tissue interactions
title_full_unstemmed Mapping the molecular and structural specialization of the skin basement membrane for inter-tissue interactions
title_short Mapping the molecular and structural specialization of the skin basement membrane for inter-tissue interactions
title_sort mapping the molecular and structural specialization of the skin basement membrane for inter-tissue interactions
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8110968/
https://www.ncbi.nlm.nih.gov/pubmed/33972551
http://dx.doi.org/10.1038/s41467-021-22881-y
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