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Bi-directional crosstalk between cells and extracellular matrix leads to network morphogenesis in multi-layered tissues

Cell-generated mechanical forces drive many cellular and tissue-level movements and rearrangements required for the tissue or organ to develop its shape(1, 2, 3, 4, 5). The prevalent view of tissue morphogenesis relies on epithelial folding resulting in compressed epithelial monolayers, overlooking...

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Autores principales: Jo, Youngmin, Yim, Donghyun, Park, Chan E, Yong, Insung, Lee, Jongbeom, Cho, Wonjin, Ahn, Kwang Ho, Yang, Chanhee, Chang, Jae-Byum, Park, Young-Gyun, Kim, Taek-Soo, Kim, Taeyoon, Kim, Pilnam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Journal Experts 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9915997/
https://www.ncbi.nlm.nih.gov/pubmed/36778230
http://dx.doi.org/10.21203/rs.3.rs-2294818/v1
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author Jo, Youngmin
Yim, Donghyun
Park, Chan E
Yong, Insung
Lee, Jongbeom
Cho, Wonjin
Ahn, Kwang Ho
Yang, Chanhee
Chang, Jae-Byum
Park, Young-Gyun
Kim, Taek-Soo
Kim, Taeyoon
Kim, Pilnam
author_facet Jo, Youngmin
Yim, Donghyun
Park, Chan E
Yong, Insung
Lee, Jongbeom
Cho, Wonjin
Ahn, Kwang Ho
Yang, Chanhee
Chang, Jae-Byum
Park, Young-Gyun
Kim, Taek-Soo
Kim, Taeyoon
Kim, Pilnam
author_sort Jo, Youngmin
collection PubMed
description Cell-generated mechanical forces drive many cellular and tissue-level movements and rearrangements required for the tissue or organ to develop its shape(1, 2, 3, 4, 5). The prevalent view of tissue morphogenesis relies on epithelial folding resulting in compressed epithelial monolayers, overlooking the involvement of stroma in morphogenesis(1, 4, 6, 7). Here, we report a giant web-like network formation of stromal cells in the epithelium-stroma interface, resulting from a multi-scale mechano-reciprocity between migrating cells and their extracellular environment. In multi-layered tissues, surface wrinkles form by a stromal cell-mediated tensional force exerted at the basement membrane. The topographical cue is transmitted to the stromal cell, directing its protrusion and migration along the wrinkles. This inductive movement of the cells conveys traction forces to its surrounding extracellular matrix, remodeling the local architectures of the stroma. In this manner, stromal cells and wrinkles communicate recursively to generate the cellular network. Our observation provides a rational mechanism for network formation in living tissues and a new understanding of the role of cellular-level tensional force in morphogenesis.
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spelling pubmed-99159972023-02-11 Bi-directional crosstalk between cells and extracellular matrix leads to network morphogenesis in multi-layered tissues Jo, Youngmin Yim, Donghyun Park, Chan E Yong, Insung Lee, Jongbeom Cho, Wonjin Ahn, Kwang Ho Yang, Chanhee Chang, Jae-Byum Park, Young-Gyun Kim, Taek-Soo Kim, Taeyoon Kim, Pilnam Res Sq Article Cell-generated mechanical forces drive many cellular and tissue-level movements and rearrangements required for the tissue or organ to develop its shape(1, 2, 3, 4, 5). The prevalent view of tissue morphogenesis relies on epithelial folding resulting in compressed epithelial monolayers, overlooking the involvement of stroma in morphogenesis(1, 4, 6, 7). Here, we report a giant web-like network formation of stromal cells in the epithelium-stroma interface, resulting from a multi-scale mechano-reciprocity between migrating cells and their extracellular environment. In multi-layered tissues, surface wrinkles form by a stromal cell-mediated tensional force exerted at the basement membrane. The topographical cue is transmitted to the stromal cell, directing its protrusion and migration along the wrinkles. This inductive movement of the cells conveys traction forces to its surrounding extracellular matrix, remodeling the local architectures of the stroma. In this manner, stromal cells and wrinkles communicate recursively to generate the cellular network. Our observation provides a rational mechanism for network formation in living tissues and a new understanding of the role of cellular-level tensional force in morphogenesis. American Journal Experts 2023-01-31 /pmc/articles/PMC9915997/ /pubmed/36778230 http://dx.doi.org/10.21203/rs.3.rs-2294818/v1 Text en https://creativecommons.org/licenses/by/4.0/This work is licensed under a Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/) , which allows reusers to distribute, remix, adapt, and build upon the material in any medium or format, so long as attribution is given to the creator. The license allows for commercial use.
spellingShingle Article
Jo, Youngmin
Yim, Donghyun
Park, Chan E
Yong, Insung
Lee, Jongbeom
Cho, Wonjin
Ahn, Kwang Ho
Yang, Chanhee
Chang, Jae-Byum
Park, Young-Gyun
Kim, Taek-Soo
Kim, Taeyoon
Kim, Pilnam
Bi-directional crosstalk between cells and extracellular matrix leads to network morphogenesis in multi-layered tissues
title Bi-directional crosstalk between cells and extracellular matrix leads to network morphogenesis in multi-layered tissues
title_full Bi-directional crosstalk between cells and extracellular matrix leads to network morphogenesis in multi-layered tissues
title_fullStr Bi-directional crosstalk between cells and extracellular matrix leads to network morphogenesis in multi-layered tissues
title_full_unstemmed Bi-directional crosstalk between cells and extracellular matrix leads to network morphogenesis in multi-layered tissues
title_short Bi-directional crosstalk between cells and extracellular matrix leads to network morphogenesis in multi-layered tissues
title_sort bi-directional crosstalk between cells and extracellular matrix leads to network morphogenesis in multi-layered tissues
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9915997/
https://www.ncbi.nlm.nih.gov/pubmed/36778230
http://dx.doi.org/10.21203/rs.3.rs-2294818/v1
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