Cargando…

Human retinal organoids release extracellular vesicles that regulate gene expression in target human retinal progenitor cells

The mechanisms underlying retinal development have not been completely elucidated. Extracellular vesicles (EVs) are novel essential mediators of cell-to-cell communication with emerging roles in developmental processes. Nevertheless, the identification of EVs in human retinal tissue, characterizatio...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhou, Jing, Flores-Bellver, Miguel, Pan, Jianbo, Benito-Martin, Alberto, Shi, Cui, Onwumere, Onyekwere, Mighty, Jason, Qian, Jiang, Zhong, Xiufeng, Hogue, Tasmim, Amponsah-Antwi, Baffour, Einbond, Linda, Gharbaran, Rajendra, Wu, Hao, Chen, Bo-Juen, Zheng, Zhiliang, Tchaikovskaya, Tatyana, Zhang, Xusheng, Peinado, Hector, Canto-Soler, Maria Valeria, Redenti, Stephen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8548301/
https://www.ncbi.nlm.nih.gov/pubmed/34702879
http://dx.doi.org/10.1038/s41598-021-00542-w
_version_ 1784590543382118400
author Zhou, Jing
Flores-Bellver, Miguel
Pan, Jianbo
Benito-Martin, Alberto
Shi, Cui
Onwumere, Onyekwere
Mighty, Jason
Qian, Jiang
Zhong, Xiufeng
Hogue, Tasmim
Amponsah-Antwi, Baffour
Einbond, Linda
Gharbaran, Rajendra
Wu, Hao
Chen, Bo-Juen
Zheng, Zhiliang
Tchaikovskaya, Tatyana
Zhang, Xusheng
Peinado, Hector
Canto-Soler, Maria Valeria
Redenti, Stephen
author_facet Zhou, Jing
Flores-Bellver, Miguel
Pan, Jianbo
Benito-Martin, Alberto
Shi, Cui
Onwumere, Onyekwere
Mighty, Jason
Qian, Jiang
Zhong, Xiufeng
Hogue, Tasmim
Amponsah-Antwi, Baffour
Einbond, Linda
Gharbaran, Rajendra
Wu, Hao
Chen, Bo-Juen
Zheng, Zhiliang
Tchaikovskaya, Tatyana
Zhang, Xusheng
Peinado, Hector
Canto-Soler, Maria Valeria
Redenti, Stephen
author_sort Zhou, Jing
collection PubMed
description The mechanisms underlying retinal development have not been completely elucidated. Extracellular vesicles (EVs) are novel essential mediators of cell-to-cell communication with emerging roles in developmental processes. Nevertheless, the identification of EVs in human retinal tissue, characterization of their cargo, and analysis of their potential role in retina development has not been accomplished. Three-dimensional retinal tissue derived from human induced pluripotent stem cells (hiPSC) provide an ideal developmental system to achieve this goal. Here we report that hiPSC-derived retinal organoids release exosomes and microvesicles with small noncoding RNA cargo. EV miRNA cargo-predicted targetome correlates with Gene Ontology (GO) pathways involved in mechanisms of retinogenesis relevant to specific developmental stages corresponding to hallmarks of native human retina development. Furthermore, uptake of EVs by human retinal progenitor cells leads to changes in gene expression correlated with EV miRNA cargo predicted gene targets, and mechanisms involved in retinal development, ganglion cell and photoreceptor differentiation and function.
format Online
Article
Text
id pubmed-8548301
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-85483012021-10-27 Human retinal organoids release extracellular vesicles that regulate gene expression in target human retinal progenitor cells Zhou, Jing Flores-Bellver, Miguel Pan, Jianbo Benito-Martin, Alberto Shi, Cui Onwumere, Onyekwere Mighty, Jason Qian, Jiang Zhong, Xiufeng Hogue, Tasmim Amponsah-Antwi, Baffour Einbond, Linda Gharbaran, Rajendra Wu, Hao Chen, Bo-Juen Zheng, Zhiliang Tchaikovskaya, Tatyana Zhang, Xusheng Peinado, Hector Canto-Soler, Maria Valeria Redenti, Stephen Sci Rep Article The mechanisms underlying retinal development have not been completely elucidated. Extracellular vesicles (EVs) are novel essential mediators of cell-to-cell communication with emerging roles in developmental processes. Nevertheless, the identification of EVs in human retinal tissue, characterization of their cargo, and analysis of their potential role in retina development has not been accomplished. Three-dimensional retinal tissue derived from human induced pluripotent stem cells (hiPSC) provide an ideal developmental system to achieve this goal. Here we report that hiPSC-derived retinal organoids release exosomes and microvesicles with small noncoding RNA cargo. EV miRNA cargo-predicted targetome correlates with Gene Ontology (GO) pathways involved in mechanisms of retinogenesis relevant to specific developmental stages corresponding to hallmarks of native human retina development. Furthermore, uptake of EVs by human retinal progenitor cells leads to changes in gene expression correlated with EV miRNA cargo predicted gene targets, and mechanisms involved in retinal development, ganglion cell and photoreceptor differentiation and function. Nature Publishing Group UK 2021-10-26 /pmc/articles/PMC8548301/ /pubmed/34702879 http://dx.doi.org/10.1038/s41598-021-00542-w Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Zhou, Jing
Flores-Bellver, Miguel
Pan, Jianbo
Benito-Martin, Alberto
Shi, Cui
Onwumere, Onyekwere
Mighty, Jason
Qian, Jiang
Zhong, Xiufeng
Hogue, Tasmim
Amponsah-Antwi, Baffour
Einbond, Linda
Gharbaran, Rajendra
Wu, Hao
Chen, Bo-Juen
Zheng, Zhiliang
Tchaikovskaya, Tatyana
Zhang, Xusheng
Peinado, Hector
Canto-Soler, Maria Valeria
Redenti, Stephen
Human retinal organoids release extracellular vesicles that regulate gene expression in target human retinal progenitor cells
title Human retinal organoids release extracellular vesicles that regulate gene expression in target human retinal progenitor cells
title_full Human retinal organoids release extracellular vesicles that regulate gene expression in target human retinal progenitor cells
title_fullStr Human retinal organoids release extracellular vesicles that regulate gene expression in target human retinal progenitor cells
title_full_unstemmed Human retinal organoids release extracellular vesicles that regulate gene expression in target human retinal progenitor cells
title_short Human retinal organoids release extracellular vesicles that regulate gene expression in target human retinal progenitor cells
title_sort human retinal organoids release extracellular vesicles that regulate gene expression in target human retinal progenitor cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8548301/
https://www.ncbi.nlm.nih.gov/pubmed/34702879
http://dx.doi.org/10.1038/s41598-021-00542-w
work_keys_str_mv AT zhoujing humanretinalorganoidsreleaseextracellularvesiclesthatregulategeneexpressionintargethumanretinalprogenitorcells
AT floresbellvermiguel humanretinalorganoidsreleaseextracellularvesiclesthatregulategeneexpressionintargethumanretinalprogenitorcells
AT panjianbo humanretinalorganoidsreleaseextracellularvesiclesthatregulategeneexpressionintargethumanretinalprogenitorcells
AT benitomartinalberto humanretinalorganoidsreleaseextracellularvesiclesthatregulategeneexpressionintargethumanretinalprogenitorcells
AT shicui humanretinalorganoidsreleaseextracellularvesiclesthatregulategeneexpressionintargethumanretinalprogenitorcells
AT onwumereonyekwere humanretinalorganoidsreleaseextracellularvesiclesthatregulategeneexpressionintargethumanretinalprogenitorcells
AT mightyjason humanretinalorganoidsreleaseextracellularvesiclesthatregulategeneexpressionintargethumanretinalprogenitorcells
AT qianjiang humanretinalorganoidsreleaseextracellularvesiclesthatregulategeneexpressionintargethumanretinalprogenitorcells
AT zhongxiufeng humanretinalorganoidsreleaseextracellularvesiclesthatregulategeneexpressionintargethumanretinalprogenitorcells
AT hoguetasmim humanretinalorganoidsreleaseextracellularvesiclesthatregulategeneexpressionintargethumanretinalprogenitorcells
AT amponsahantwibaffour humanretinalorganoidsreleaseextracellularvesiclesthatregulategeneexpressionintargethumanretinalprogenitorcells
AT einbondlinda humanretinalorganoidsreleaseextracellularvesiclesthatregulategeneexpressionintargethumanretinalprogenitorcells
AT gharbaranrajendra humanretinalorganoidsreleaseextracellularvesiclesthatregulategeneexpressionintargethumanretinalprogenitorcells
AT wuhao humanretinalorganoidsreleaseextracellularvesiclesthatregulategeneexpressionintargethumanretinalprogenitorcells
AT chenbojuen humanretinalorganoidsreleaseextracellularvesiclesthatregulategeneexpressionintargethumanretinalprogenitorcells
AT zhengzhiliang humanretinalorganoidsreleaseextracellularvesiclesthatregulategeneexpressionintargethumanretinalprogenitorcells
AT tchaikovskayatatyana humanretinalorganoidsreleaseextracellularvesiclesthatregulategeneexpressionintargethumanretinalprogenitorcells
AT zhangxusheng humanretinalorganoidsreleaseextracellularvesiclesthatregulategeneexpressionintargethumanretinalprogenitorcells
AT peinadohector humanretinalorganoidsreleaseextracellularvesiclesthatregulategeneexpressionintargethumanretinalprogenitorcells
AT cantosolermariavaleria humanretinalorganoidsreleaseextracellularvesiclesthatregulategeneexpressionintargethumanretinalprogenitorcells
AT redentistephen humanretinalorganoidsreleaseextracellularvesiclesthatregulategeneexpressionintargethumanretinalprogenitorcells