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An apicosome initiates self-organizing morphogenesis of human pluripotent stem cells

Human pluripotent stem cells (hPSCs) self-organize into apicobasally polarized cysts, reminiscent of the lumenal epiblast stage, providing a model to explore key morphogenic processes in early human embryos. Here, we show that apical polarization begins on the interior of single hPSCs through the dy...

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Autores principales: Taniguchi, Kenichiro, Shao, Yue, Townshend, Ryan F., Cortez, Chari L., Harris, Clair E., Meshinchi, Sasha, Kalantry, Sundeep, Fu, Jianping, O’Shea, K. Sue, Gumucio, Deborah L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5716285/
https://www.ncbi.nlm.nih.gov/pubmed/29021220
http://dx.doi.org/10.1083/jcb.201704085
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author Taniguchi, Kenichiro
Shao, Yue
Townshend, Ryan F.
Cortez, Chari L.
Harris, Clair E.
Meshinchi, Sasha
Kalantry, Sundeep
Fu, Jianping
O’Shea, K. Sue
Gumucio, Deborah L.
author_facet Taniguchi, Kenichiro
Shao, Yue
Townshend, Ryan F.
Cortez, Chari L.
Harris, Clair E.
Meshinchi, Sasha
Kalantry, Sundeep
Fu, Jianping
O’Shea, K. Sue
Gumucio, Deborah L.
author_sort Taniguchi, Kenichiro
collection PubMed
description Human pluripotent stem cells (hPSCs) self-organize into apicobasally polarized cysts, reminiscent of the lumenal epiblast stage, providing a model to explore key morphogenic processes in early human embryos. Here, we show that apical polarization begins on the interior of single hPSCs through the dynamic formation of a highly organized perinuclear apicosome structure. The membrane surrounding the apicosome is enriched in apical markers and displays microvilli and a primary cilium; its lumenal space is rich in Ca(2+). Time-lapse imaging of isolated hPSCs reveals that the apicosome forms de novo in interphase, retains its structure during mitosis, is asymmetrically inherited after mitosis, and relocates to the recently formed cytokinetic plane, where it establishes a fully polarized lumen. In a multicellular aggregate of hPSCs, intracellular apicosomes from multiple cells are trafficked to generate a common lumenal cavity. Thus, the apicosome is a unique preassembled apical structure that can be rapidly used in single or clustered hPSCs to initiate self-organized apical polarization and lumenogenesis.
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spelling pubmed-57162852018-06-04 An apicosome initiates self-organizing morphogenesis of human pluripotent stem cells Taniguchi, Kenichiro Shao, Yue Townshend, Ryan F. Cortez, Chari L. Harris, Clair E. Meshinchi, Sasha Kalantry, Sundeep Fu, Jianping O’Shea, K. Sue Gumucio, Deborah L. J Cell Biol Research Articles Human pluripotent stem cells (hPSCs) self-organize into apicobasally polarized cysts, reminiscent of the lumenal epiblast stage, providing a model to explore key morphogenic processes in early human embryos. Here, we show that apical polarization begins on the interior of single hPSCs through the dynamic formation of a highly organized perinuclear apicosome structure. The membrane surrounding the apicosome is enriched in apical markers and displays microvilli and a primary cilium; its lumenal space is rich in Ca(2+). Time-lapse imaging of isolated hPSCs reveals that the apicosome forms de novo in interphase, retains its structure during mitosis, is asymmetrically inherited after mitosis, and relocates to the recently formed cytokinetic plane, where it establishes a fully polarized lumen. In a multicellular aggregate of hPSCs, intracellular apicosomes from multiple cells are trafficked to generate a common lumenal cavity. Thus, the apicosome is a unique preassembled apical structure that can be rapidly used in single or clustered hPSCs to initiate self-organized apical polarization and lumenogenesis. The Rockefeller University Press 2017-12-04 /pmc/articles/PMC5716285/ /pubmed/29021220 http://dx.doi.org/10.1083/jcb.201704085 Text en © 2017 Taniguchi et al. http://www.rupress.org/terms/https://creativecommons.org/licenses/by-nc-sa/4.0/This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms/). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 International license, as described at https://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Research Articles
Taniguchi, Kenichiro
Shao, Yue
Townshend, Ryan F.
Cortez, Chari L.
Harris, Clair E.
Meshinchi, Sasha
Kalantry, Sundeep
Fu, Jianping
O’Shea, K. Sue
Gumucio, Deborah L.
An apicosome initiates self-organizing morphogenesis of human pluripotent stem cells
title An apicosome initiates self-organizing morphogenesis of human pluripotent stem cells
title_full An apicosome initiates self-organizing morphogenesis of human pluripotent stem cells
title_fullStr An apicosome initiates self-organizing morphogenesis of human pluripotent stem cells
title_full_unstemmed An apicosome initiates self-organizing morphogenesis of human pluripotent stem cells
title_short An apicosome initiates self-organizing morphogenesis of human pluripotent stem cells
title_sort apicosome initiates self-organizing morphogenesis of human pluripotent stem cells
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5716285/
https://www.ncbi.nlm.nih.gov/pubmed/29021220
http://dx.doi.org/10.1083/jcb.201704085
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