Cargando…

Enhanced Inner-Ear Organoid Formation from Mouse Embryonic Stem Cells by Photobiomodulation

Photobiomodulation (PBM) stimulates different types of stem cells to migrate, proliferate, and differentiate in vitro and in vivo. However, little is known about the effects of PBM on the differentiation of embryonic stem cells (ESCs) toward the otic lineage. Only a few reports have documented the i...

Descripción completa

Detalles Bibliográficos
Autores principales: Chang, So-Young, Carpena, Nathaniel T., Mun, Seyoung, Jung, Jae Yun, Chung, Phil-Sang, Shim, Hosup, Han, Kyudong, Ahn, Jin-Chul, Lee, Min Young
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society of Gene & Cell Therapy 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7118273/
https://www.ncbi.nlm.nih.gov/pubmed/32258218
http://dx.doi.org/10.1016/j.omtm.2020.03.010
_version_ 1783514526541414400
author Chang, So-Young
Carpena, Nathaniel T.
Mun, Seyoung
Jung, Jae Yun
Chung, Phil-Sang
Shim, Hosup
Han, Kyudong
Ahn, Jin-Chul
Lee, Min Young
author_facet Chang, So-Young
Carpena, Nathaniel T.
Mun, Seyoung
Jung, Jae Yun
Chung, Phil-Sang
Shim, Hosup
Han, Kyudong
Ahn, Jin-Chul
Lee, Min Young
author_sort Chang, So-Young
collection PubMed
description Photobiomodulation (PBM) stimulates different types of stem cells to migrate, proliferate, and differentiate in vitro and in vivo. However, little is known about the effects of PBM on the differentiation of embryonic stem cells (ESCs) toward the otic lineage. Only a few reports have documented the in vitro differentiation of ESCs into inner-ear hair cells (HCs) due to the complexity of HCs compared with other target cell types. In this study, we determined the optimal condition to differentiate the ESCs into the otic organoid using different culture techniques and PBM parameters. The efficiency of organoid formation within the embryoid body (EB) was dependent on the cell density of the hanging drop. PBM, using 630 nm wavelength light-emitting diodes (LEDs), further improved the differentiation of inner-ear hair cell-like cells coupled with reactive oxygen species (ROS) overexpression. Transcriptome analysis showed the factors that are responsible for the effect of PBM in the formation of otic organoids, notably, the downregulation of neural development-associated genes and the hairy and enhancer of split 5 (Hes5) gene, which inhibits the differentiation of prosensory cells to hair cells. These data enrich the current differentiation protocols for generating inner-ear hair cells.
format Online
Article
Text
id pubmed-7118273
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher American Society of Gene & Cell Therapy
record_format MEDLINE/PubMed
spelling pubmed-71182732020-04-06 Enhanced Inner-Ear Organoid Formation from Mouse Embryonic Stem Cells by Photobiomodulation Chang, So-Young Carpena, Nathaniel T. Mun, Seyoung Jung, Jae Yun Chung, Phil-Sang Shim, Hosup Han, Kyudong Ahn, Jin-Chul Lee, Min Young Mol Ther Methods Clin Dev Article Photobiomodulation (PBM) stimulates different types of stem cells to migrate, proliferate, and differentiate in vitro and in vivo. However, little is known about the effects of PBM on the differentiation of embryonic stem cells (ESCs) toward the otic lineage. Only a few reports have documented the in vitro differentiation of ESCs into inner-ear hair cells (HCs) due to the complexity of HCs compared with other target cell types. In this study, we determined the optimal condition to differentiate the ESCs into the otic organoid using different culture techniques and PBM parameters. The efficiency of organoid formation within the embryoid body (EB) was dependent on the cell density of the hanging drop. PBM, using 630 nm wavelength light-emitting diodes (LEDs), further improved the differentiation of inner-ear hair cell-like cells coupled with reactive oxygen species (ROS) overexpression. Transcriptome analysis showed the factors that are responsible for the effect of PBM in the formation of otic organoids, notably, the downregulation of neural development-associated genes and the hairy and enhancer of split 5 (Hes5) gene, which inhibits the differentiation of prosensory cells to hair cells. These data enrich the current differentiation protocols for generating inner-ear hair cells. American Society of Gene & Cell Therapy 2020-03-13 /pmc/articles/PMC7118273/ /pubmed/32258218 http://dx.doi.org/10.1016/j.omtm.2020.03.010 Text en © 2020 The Author(s) http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Chang, So-Young
Carpena, Nathaniel T.
Mun, Seyoung
Jung, Jae Yun
Chung, Phil-Sang
Shim, Hosup
Han, Kyudong
Ahn, Jin-Chul
Lee, Min Young
Enhanced Inner-Ear Organoid Formation from Mouse Embryonic Stem Cells by Photobiomodulation
title Enhanced Inner-Ear Organoid Formation from Mouse Embryonic Stem Cells by Photobiomodulation
title_full Enhanced Inner-Ear Organoid Formation from Mouse Embryonic Stem Cells by Photobiomodulation
title_fullStr Enhanced Inner-Ear Organoid Formation from Mouse Embryonic Stem Cells by Photobiomodulation
title_full_unstemmed Enhanced Inner-Ear Organoid Formation from Mouse Embryonic Stem Cells by Photobiomodulation
title_short Enhanced Inner-Ear Organoid Formation from Mouse Embryonic Stem Cells by Photobiomodulation
title_sort enhanced inner-ear organoid formation from mouse embryonic stem cells by photobiomodulation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7118273/
https://www.ncbi.nlm.nih.gov/pubmed/32258218
http://dx.doi.org/10.1016/j.omtm.2020.03.010
work_keys_str_mv AT changsoyoung enhancedinnerearorganoidformationfrommouseembryonicstemcellsbyphotobiomodulation
AT carpenanathanielt enhancedinnerearorganoidformationfrommouseembryonicstemcellsbyphotobiomodulation
AT munseyoung enhancedinnerearorganoidformationfrommouseembryonicstemcellsbyphotobiomodulation
AT jungjaeyun enhancedinnerearorganoidformationfrommouseembryonicstemcellsbyphotobiomodulation
AT chungphilsang enhancedinnerearorganoidformationfrommouseembryonicstemcellsbyphotobiomodulation
AT shimhosup enhancedinnerearorganoidformationfrommouseembryonicstemcellsbyphotobiomodulation
AT hankyudong enhancedinnerearorganoidformationfrommouseembryonicstemcellsbyphotobiomodulation
AT ahnjinchul enhancedinnerearorganoidformationfrommouseembryonicstemcellsbyphotobiomodulation
AT leeminyoung enhancedinnerearorganoidformationfrommouseembryonicstemcellsbyphotobiomodulation