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Generation of Skeletal Muscle Organoids from Human Pluripotent Stem Cells to Model Myogenesis and Muscle Regeneration

In vitro organoids derived from human pluripotent stem cells (hPSCs) have been developed as essential tools to study the underlying mechanisms of human development and diseases owing to their structural and physiological similarity to corresponding organs. Despite recent advances, there are a few me...

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Autores principales: Shin, Min-Kyoung, Bang, Jin Seok, Lee, Jeoung Eun, Tran, Hoang-Dai, Park, Genehong, Lee, Dong Ryul, Jo, Junghyun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9103168/
https://www.ncbi.nlm.nih.gov/pubmed/35563499
http://dx.doi.org/10.3390/ijms23095108
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author Shin, Min-Kyoung
Bang, Jin Seok
Lee, Jeoung Eun
Tran, Hoang-Dai
Park, Genehong
Lee, Dong Ryul
Jo, Junghyun
author_facet Shin, Min-Kyoung
Bang, Jin Seok
Lee, Jeoung Eun
Tran, Hoang-Dai
Park, Genehong
Lee, Dong Ryul
Jo, Junghyun
author_sort Shin, Min-Kyoung
collection PubMed
description In vitro organoids derived from human pluripotent stem cells (hPSCs) have been developed as essential tools to study the underlying mechanisms of human development and diseases owing to their structural and physiological similarity to corresponding organs. Despite recent advances, there are a few methodologies for three-dimensional (3D) skeletal muscle differentiation, which focus on the terminal differentiation into myofibers and investigate the potential of modeling neuromuscular disorders and muscular dystrophies. However, these methodologies cannot recapitulate the developmental processes and lack regenerative capacity. In this study, we developed a new method to differentiate hPSCs into a 3D human skeletal muscle organoid (hSkMO). This organoid model could recapitulate the myogenesis process and possesses regenerative capacities of sustainable satellite cells (SCs), which are adult muscle stem/progenitor cells capable of self-renewal and myogenic differentiation. Our 3D model demonstrated myogenesis through the sequential occurrence of multiple myogenic cell types from SCs to myocytes. Notably, we detected quiescent, non-dividing SCs throughout the hSkMO differentiation in long-term culture. They were activated and differentiated to reconstitute muscle tissue upon damage. Thus, hSkMOs can recapitulate human skeletal muscle development and regeneration and may provide a new model for studying human skeletal muscles and related diseases.
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spelling pubmed-91031682022-05-14 Generation of Skeletal Muscle Organoids from Human Pluripotent Stem Cells to Model Myogenesis and Muscle Regeneration Shin, Min-Kyoung Bang, Jin Seok Lee, Jeoung Eun Tran, Hoang-Dai Park, Genehong Lee, Dong Ryul Jo, Junghyun Int J Mol Sci Article In vitro organoids derived from human pluripotent stem cells (hPSCs) have been developed as essential tools to study the underlying mechanisms of human development and diseases owing to their structural and physiological similarity to corresponding organs. Despite recent advances, there are a few methodologies for three-dimensional (3D) skeletal muscle differentiation, which focus on the terminal differentiation into myofibers and investigate the potential of modeling neuromuscular disorders and muscular dystrophies. However, these methodologies cannot recapitulate the developmental processes and lack regenerative capacity. In this study, we developed a new method to differentiate hPSCs into a 3D human skeletal muscle organoid (hSkMO). This organoid model could recapitulate the myogenesis process and possesses regenerative capacities of sustainable satellite cells (SCs), which are adult muscle stem/progenitor cells capable of self-renewal and myogenic differentiation. Our 3D model demonstrated myogenesis through the sequential occurrence of multiple myogenic cell types from SCs to myocytes. Notably, we detected quiescent, non-dividing SCs throughout the hSkMO differentiation in long-term culture. They were activated and differentiated to reconstitute muscle tissue upon damage. Thus, hSkMOs can recapitulate human skeletal muscle development and regeneration and may provide a new model for studying human skeletal muscles and related diseases. MDPI 2022-05-04 /pmc/articles/PMC9103168/ /pubmed/35563499 http://dx.doi.org/10.3390/ijms23095108 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Shin, Min-Kyoung
Bang, Jin Seok
Lee, Jeoung Eun
Tran, Hoang-Dai
Park, Genehong
Lee, Dong Ryul
Jo, Junghyun
Generation of Skeletal Muscle Organoids from Human Pluripotent Stem Cells to Model Myogenesis and Muscle Regeneration
title Generation of Skeletal Muscle Organoids from Human Pluripotent Stem Cells to Model Myogenesis and Muscle Regeneration
title_full Generation of Skeletal Muscle Organoids from Human Pluripotent Stem Cells to Model Myogenesis and Muscle Regeneration
title_fullStr Generation of Skeletal Muscle Organoids from Human Pluripotent Stem Cells to Model Myogenesis and Muscle Regeneration
title_full_unstemmed Generation of Skeletal Muscle Organoids from Human Pluripotent Stem Cells to Model Myogenesis and Muscle Regeneration
title_short Generation of Skeletal Muscle Organoids from Human Pluripotent Stem Cells to Model Myogenesis and Muscle Regeneration
title_sort generation of skeletal muscle organoids from human pluripotent stem cells to model myogenesis and muscle regeneration
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9103168/
https://www.ncbi.nlm.nih.gov/pubmed/35563499
http://dx.doi.org/10.3390/ijms23095108
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