Cargando…

Symmetry Breaking of Human Pluripotent Stem Cells (hPSCs) in Micropattern Generates a Polarized Spinal Cord‐Like Organoid (pSCO) with Dorsoventral Organization

Axis formation and related spatial patterning are initiated by symmetry breaking during development. A geometrically confined culture of human pluripotent stem cells (hPSCs) mimics symmetry breaking and cell patterning. Using this, polarized spinal cord organoids (pSCOs) with a self‐organized dorsov...

Descripción completa

Detalles Bibliográficos
Autores principales: Seo, Kyubin, Cho, Subin, Shin, Hyogeun, Shin, Aeri, Lee, Ju‐Hyun, Kim, June Hoan, Lee, Boram, Jang, Hwanseok, Kim, Youngju, Cho, Hyo Min, Park, Yongdoo, Kim, Hee Youn, Lee, Taeseob, Park, Woong‐Yang, Kim, Yong Jun, Yang, Esther, Geum, Dongho, Kim, Hyun, Cho, Il‐Joo, Lee, Sanghyuk, Ryu, Jae Ryun, Sun, Woong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10369253/
https://www.ncbi.nlm.nih.gov/pubmed/37170679
http://dx.doi.org/10.1002/advs.202301787
_version_ 1785077718292889600
author Seo, Kyubin
Cho, Subin
Shin, Hyogeun
Shin, Aeri
Lee, Ju‐Hyun
Kim, June Hoan
Lee, Boram
Jang, Hwanseok
Kim, Youngju
Cho, Hyo Min
Park, Yongdoo
Kim, Hee Youn
Lee, Taeseob
Park, Woong‐Yang
Kim, Yong Jun
Yang, Esther
Geum, Dongho
Kim, Hyun
Cho, Il‐Joo
Lee, Sanghyuk
Ryu, Jae Ryun
Sun, Woong
author_facet Seo, Kyubin
Cho, Subin
Shin, Hyogeun
Shin, Aeri
Lee, Ju‐Hyun
Kim, June Hoan
Lee, Boram
Jang, Hwanseok
Kim, Youngju
Cho, Hyo Min
Park, Yongdoo
Kim, Hee Youn
Lee, Taeseob
Park, Woong‐Yang
Kim, Yong Jun
Yang, Esther
Geum, Dongho
Kim, Hyun
Cho, Il‐Joo
Lee, Sanghyuk
Ryu, Jae Ryun
Sun, Woong
author_sort Seo, Kyubin
collection PubMed
description Axis formation and related spatial patterning are initiated by symmetry breaking during development. A geometrically confined culture of human pluripotent stem cells (hPSCs) mimics symmetry breaking and cell patterning. Using this, polarized spinal cord organoids (pSCOs) with a self‐organized dorsoventral (DV) organization are generated. The application of caudalization signals promoted regionalized cell differentiation along the radial axis and protrusion morphogenesis in confined hPSC colonies. These detached colonies grew into extended spinal cord‐like organoids, which established self‐ordered DV patterning along the long axis through the spontaneous expression of polarized DV patterning morphogens. The proportions of dorsal/ventral domains in the pSCOs can be controlled by the changes in the initial size of micropatterns, which altered the ratio of center‐edge cells in 2D. In mature pSCOs, highly synchronized neural activity is separately detected in the dorsal and ventral side, indicating functional as well as structural patterning established in the organoids. This study provides a simple and precisely controllable method to generate spatially ordered organoids for the understanding of the biological principles of cell patterning and axis formation during neural development.
format Online
Article
Text
id pubmed-10369253
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-103692532023-07-27 Symmetry Breaking of Human Pluripotent Stem Cells (hPSCs) in Micropattern Generates a Polarized Spinal Cord‐Like Organoid (pSCO) with Dorsoventral Organization Seo, Kyubin Cho, Subin Shin, Hyogeun Shin, Aeri Lee, Ju‐Hyun Kim, June Hoan Lee, Boram Jang, Hwanseok Kim, Youngju Cho, Hyo Min Park, Yongdoo Kim, Hee Youn Lee, Taeseob Park, Woong‐Yang Kim, Yong Jun Yang, Esther Geum, Dongho Kim, Hyun Cho, Il‐Joo Lee, Sanghyuk Ryu, Jae Ryun Sun, Woong Adv Sci (Weinh) Research Articles Axis formation and related spatial patterning are initiated by symmetry breaking during development. A geometrically confined culture of human pluripotent stem cells (hPSCs) mimics symmetry breaking and cell patterning. Using this, polarized spinal cord organoids (pSCOs) with a self‐organized dorsoventral (DV) organization are generated. The application of caudalization signals promoted regionalized cell differentiation along the radial axis and protrusion morphogenesis in confined hPSC colonies. These detached colonies grew into extended spinal cord‐like organoids, which established self‐ordered DV patterning along the long axis through the spontaneous expression of polarized DV patterning morphogens. The proportions of dorsal/ventral domains in the pSCOs can be controlled by the changes in the initial size of micropatterns, which altered the ratio of center‐edge cells in 2D. In mature pSCOs, highly synchronized neural activity is separately detected in the dorsal and ventral side, indicating functional as well as structural patterning established in the organoids. This study provides a simple and precisely controllable method to generate spatially ordered organoids for the understanding of the biological principles of cell patterning and axis formation during neural development. John Wiley and Sons Inc. 2023-05-12 /pmc/articles/PMC10369253/ /pubmed/37170679 http://dx.doi.org/10.1002/advs.202301787 Text en © 2023 The Authors. Advanced Science published by Wiley‐VCH GmbH https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Seo, Kyubin
Cho, Subin
Shin, Hyogeun
Shin, Aeri
Lee, Ju‐Hyun
Kim, June Hoan
Lee, Boram
Jang, Hwanseok
Kim, Youngju
Cho, Hyo Min
Park, Yongdoo
Kim, Hee Youn
Lee, Taeseob
Park, Woong‐Yang
Kim, Yong Jun
Yang, Esther
Geum, Dongho
Kim, Hyun
Cho, Il‐Joo
Lee, Sanghyuk
Ryu, Jae Ryun
Sun, Woong
Symmetry Breaking of Human Pluripotent Stem Cells (hPSCs) in Micropattern Generates a Polarized Spinal Cord‐Like Organoid (pSCO) with Dorsoventral Organization
title Symmetry Breaking of Human Pluripotent Stem Cells (hPSCs) in Micropattern Generates a Polarized Spinal Cord‐Like Organoid (pSCO) with Dorsoventral Organization
title_full Symmetry Breaking of Human Pluripotent Stem Cells (hPSCs) in Micropattern Generates a Polarized Spinal Cord‐Like Organoid (pSCO) with Dorsoventral Organization
title_fullStr Symmetry Breaking of Human Pluripotent Stem Cells (hPSCs) in Micropattern Generates a Polarized Spinal Cord‐Like Organoid (pSCO) with Dorsoventral Organization
title_full_unstemmed Symmetry Breaking of Human Pluripotent Stem Cells (hPSCs) in Micropattern Generates a Polarized Spinal Cord‐Like Organoid (pSCO) with Dorsoventral Organization
title_short Symmetry Breaking of Human Pluripotent Stem Cells (hPSCs) in Micropattern Generates a Polarized Spinal Cord‐Like Organoid (pSCO) with Dorsoventral Organization
title_sort symmetry breaking of human pluripotent stem cells (hpscs) in micropattern generates a polarized spinal cord‐like organoid (psco) with dorsoventral organization
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10369253/
https://www.ncbi.nlm.nih.gov/pubmed/37170679
http://dx.doi.org/10.1002/advs.202301787
work_keys_str_mv AT seokyubin symmetrybreakingofhumanpluripotentstemcellshpscsinmicropatterngeneratesapolarizedspinalcordlikeorganoidpscowithdorsoventralorganization
AT chosubin symmetrybreakingofhumanpluripotentstemcellshpscsinmicropatterngeneratesapolarizedspinalcordlikeorganoidpscowithdorsoventralorganization
AT shinhyogeun symmetrybreakingofhumanpluripotentstemcellshpscsinmicropatterngeneratesapolarizedspinalcordlikeorganoidpscowithdorsoventralorganization
AT shinaeri symmetrybreakingofhumanpluripotentstemcellshpscsinmicropatterngeneratesapolarizedspinalcordlikeorganoidpscowithdorsoventralorganization
AT leejuhyun symmetrybreakingofhumanpluripotentstemcellshpscsinmicropatterngeneratesapolarizedspinalcordlikeorganoidpscowithdorsoventralorganization
AT kimjunehoan symmetrybreakingofhumanpluripotentstemcellshpscsinmicropatterngeneratesapolarizedspinalcordlikeorganoidpscowithdorsoventralorganization
AT leeboram symmetrybreakingofhumanpluripotentstemcellshpscsinmicropatterngeneratesapolarizedspinalcordlikeorganoidpscowithdorsoventralorganization
AT janghwanseok symmetrybreakingofhumanpluripotentstemcellshpscsinmicropatterngeneratesapolarizedspinalcordlikeorganoidpscowithdorsoventralorganization
AT kimyoungju symmetrybreakingofhumanpluripotentstemcellshpscsinmicropatterngeneratesapolarizedspinalcordlikeorganoidpscowithdorsoventralorganization
AT chohyomin symmetrybreakingofhumanpluripotentstemcellshpscsinmicropatterngeneratesapolarizedspinalcordlikeorganoidpscowithdorsoventralorganization
AT parkyongdoo symmetrybreakingofhumanpluripotentstemcellshpscsinmicropatterngeneratesapolarizedspinalcordlikeorganoidpscowithdorsoventralorganization
AT kimheeyoun symmetrybreakingofhumanpluripotentstemcellshpscsinmicropatterngeneratesapolarizedspinalcordlikeorganoidpscowithdorsoventralorganization
AT leetaeseob symmetrybreakingofhumanpluripotentstemcellshpscsinmicropatterngeneratesapolarizedspinalcordlikeorganoidpscowithdorsoventralorganization
AT parkwoongyang symmetrybreakingofhumanpluripotentstemcellshpscsinmicropatterngeneratesapolarizedspinalcordlikeorganoidpscowithdorsoventralorganization
AT kimyongjun symmetrybreakingofhumanpluripotentstemcellshpscsinmicropatterngeneratesapolarizedspinalcordlikeorganoidpscowithdorsoventralorganization
AT yangesther symmetrybreakingofhumanpluripotentstemcellshpscsinmicropatterngeneratesapolarizedspinalcordlikeorganoidpscowithdorsoventralorganization
AT geumdongho symmetrybreakingofhumanpluripotentstemcellshpscsinmicropatterngeneratesapolarizedspinalcordlikeorganoidpscowithdorsoventralorganization
AT kimhyun symmetrybreakingofhumanpluripotentstemcellshpscsinmicropatterngeneratesapolarizedspinalcordlikeorganoidpscowithdorsoventralorganization
AT choiljoo symmetrybreakingofhumanpluripotentstemcellshpscsinmicropatterngeneratesapolarizedspinalcordlikeorganoidpscowithdorsoventralorganization
AT leesanghyuk symmetrybreakingofhumanpluripotentstemcellshpscsinmicropatterngeneratesapolarizedspinalcordlikeorganoidpscowithdorsoventralorganization
AT ryujaeryun symmetrybreakingofhumanpluripotentstemcellshpscsinmicropatterngeneratesapolarizedspinalcordlikeorganoidpscowithdorsoventralorganization
AT sunwoong symmetrybreakingofhumanpluripotentstemcellshpscsinmicropatterngeneratesapolarizedspinalcordlikeorganoidpscowithdorsoventralorganization