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Control of matrix stiffness promotes endodermal lineage specification by regulating SMAD2/3 via lncRNA LINC00458

During endoderm formation, cell identity and tissue morphogenesis are tightly controlled by cell-intrinsic and cell-extrinsic factors such as biochemical and physical inputs. While the effects of biochemical factors are well studied, the physical cues that regulate cell division and differentiation...

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Autores principales: Chen, Yu-Fan, Li, Yi-Shuan J., Chou, Chih-Hung, Chiew, Men Yee, Huang, Hsien-Da, Ho, Jennifer Hui-Chun, Chien, Shu, Lee, Oscar K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7002135/
https://www.ncbi.nlm.nih.gov/pubmed/32076643
http://dx.doi.org/10.1126/sciadv.aay0264
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author Chen, Yu-Fan
Li, Yi-Shuan J.
Chou, Chih-Hung
Chiew, Men Yee
Huang, Hsien-Da
Ho, Jennifer Hui-Chun
Chien, Shu
Lee, Oscar K.
author_facet Chen, Yu-Fan
Li, Yi-Shuan J.
Chou, Chih-Hung
Chiew, Men Yee
Huang, Hsien-Da
Ho, Jennifer Hui-Chun
Chien, Shu
Lee, Oscar K.
author_sort Chen, Yu-Fan
collection PubMed
description During endoderm formation, cell identity and tissue morphogenesis are tightly controlled by cell-intrinsic and cell-extrinsic factors such as biochemical and physical inputs. While the effects of biochemical factors are well studied, the physical cues that regulate cell division and differentiation are poorly understood. RNA sequencing analysis demonstrated increases of endoderm-specific gene expression in hPSCs cultured on soft substrate (Young’s modulus, 3 ± 0.45 kPa) in comparison with hard substrate (Young’s modulus, 165 ± 6.39 kPa). Further analyses revealed that multiple long noncoding RNAs (lncRNAs) were up-regulated on soft substrate; among them, LINC00458 was identified as a stiffness-dependent lncRNA specifically required for hPSC differentiation toward an early endodermal lineage. Gain- and loss-of-function experiments confirmed that LINC00458 is functionally required for hPSC endodermal lineage specification induced by soft substrates. Our study provides evidence that mechanical cues regulate the expression of LINC00458 and induce differentiation of hPSC into hepatic lineage progenitors.
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spelling pubmed-70021352020-02-19 Control of matrix stiffness promotes endodermal lineage specification by regulating SMAD2/3 via lncRNA LINC00458 Chen, Yu-Fan Li, Yi-Shuan J. Chou, Chih-Hung Chiew, Men Yee Huang, Hsien-Da Ho, Jennifer Hui-Chun Chien, Shu Lee, Oscar K. Sci Adv Research Articles During endoderm formation, cell identity and tissue morphogenesis are tightly controlled by cell-intrinsic and cell-extrinsic factors such as biochemical and physical inputs. While the effects of biochemical factors are well studied, the physical cues that regulate cell division and differentiation are poorly understood. RNA sequencing analysis demonstrated increases of endoderm-specific gene expression in hPSCs cultured on soft substrate (Young’s modulus, 3 ± 0.45 kPa) in comparison with hard substrate (Young’s modulus, 165 ± 6.39 kPa). Further analyses revealed that multiple long noncoding RNAs (lncRNAs) were up-regulated on soft substrate; among them, LINC00458 was identified as a stiffness-dependent lncRNA specifically required for hPSC differentiation toward an early endodermal lineage. Gain- and loss-of-function experiments confirmed that LINC00458 is functionally required for hPSC endodermal lineage specification induced by soft substrates. Our study provides evidence that mechanical cues regulate the expression of LINC00458 and induce differentiation of hPSC into hepatic lineage progenitors. American Association for the Advancement of Science 2020-02-05 /pmc/articles/PMC7002135/ /pubmed/32076643 http://dx.doi.org/10.1126/sciadv.aay0264 Text en Copyright © 2020 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). http://creativecommons.org/licenses/by-nc/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (http://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited.
spellingShingle Research Articles
Chen, Yu-Fan
Li, Yi-Shuan J.
Chou, Chih-Hung
Chiew, Men Yee
Huang, Hsien-Da
Ho, Jennifer Hui-Chun
Chien, Shu
Lee, Oscar K.
Control of matrix stiffness promotes endodermal lineage specification by regulating SMAD2/3 via lncRNA LINC00458
title Control of matrix stiffness promotes endodermal lineage specification by regulating SMAD2/3 via lncRNA LINC00458
title_full Control of matrix stiffness promotes endodermal lineage specification by regulating SMAD2/3 via lncRNA LINC00458
title_fullStr Control of matrix stiffness promotes endodermal lineage specification by regulating SMAD2/3 via lncRNA LINC00458
title_full_unstemmed Control of matrix stiffness promotes endodermal lineage specification by regulating SMAD2/3 via lncRNA LINC00458
title_short Control of matrix stiffness promotes endodermal lineage specification by regulating SMAD2/3 via lncRNA LINC00458
title_sort control of matrix stiffness promotes endodermal lineage specification by regulating smad2/3 via lncrna linc00458
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7002135/
https://www.ncbi.nlm.nih.gov/pubmed/32076643
http://dx.doi.org/10.1126/sciadv.aay0264
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