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Single-Cell Transcriptomic Comparison of Human Fetal Retina, hPSC-Derived Retinal Organoids, and Long-Term Retinal Cultures

To study the development of the human retina, we use single-cell RNA sequencing (RNA-seq) at key fetal stages and follow the development of the major cell types as well as populations of transitional cells. We also analyze stem cell (hPSC)-derived retinal organoids; although organoids have a very si...

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Autores principales: Sridhar, Akshayalakshmi, Hoshino, Akina, Finkbeiner, Connor R., Chitsazan, Alex, Dai, Li, Haugan, Alexandra K., Eschenbacher, Kayla M., Jackson, Dana L., Trapnell, Cole, Bermingham-McDonogh, Olivia, Glass, Ian, Reh, Thomas A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7901645/
https://www.ncbi.nlm.nih.gov/pubmed/32023475
http://dx.doi.org/10.1016/j.celrep.2020.01.007
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author Sridhar, Akshayalakshmi
Hoshino, Akina
Finkbeiner, Connor R.
Chitsazan, Alex
Dai, Li
Haugan, Alexandra K.
Eschenbacher, Kayla M.
Jackson, Dana L.
Trapnell, Cole
Bermingham-McDonogh, Olivia
Glass, Ian
Reh, Thomas A.
author_facet Sridhar, Akshayalakshmi
Hoshino, Akina
Finkbeiner, Connor R.
Chitsazan, Alex
Dai, Li
Haugan, Alexandra K.
Eschenbacher, Kayla M.
Jackson, Dana L.
Trapnell, Cole
Bermingham-McDonogh, Olivia
Glass, Ian
Reh, Thomas A.
author_sort Sridhar, Akshayalakshmi
collection PubMed
description To study the development of the human retina, we use single-cell RNA sequencing (RNA-seq) at key fetal stages and follow the development of the major cell types as well as populations of transitional cells. We also analyze stem cell (hPSC)-derived retinal organoids; although organoids have a very similar cellular composition at equivalent ages as the fetal retina, there are some differences in gene expression of particular cell types. Moreover, the inner retinal lamination is disrupted at more advanced stages of organoids compared with fetal retina. To determine whether the disorganization in the inner retina is due to the culture conditions, we analyze retinal development in fetal retina maintained under similar conditions. These retinospheres develop for at least 6 months, displaying better inner retinal lamination than retinal organoids. Our single-cell RNA sequencing (scRNA-seq) comparisons of fetal retina, retinal organoids, and retinospheres provide a resource for developing better in vitro models for retinal disease.
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spelling pubmed-79016452021-02-23 Single-Cell Transcriptomic Comparison of Human Fetal Retina, hPSC-Derived Retinal Organoids, and Long-Term Retinal Cultures Sridhar, Akshayalakshmi Hoshino, Akina Finkbeiner, Connor R. Chitsazan, Alex Dai, Li Haugan, Alexandra K. Eschenbacher, Kayla M. Jackson, Dana L. Trapnell, Cole Bermingham-McDonogh, Olivia Glass, Ian Reh, Thomas A. Cell Rep Article To study the development of the human retina, we use single-cell RNA sequencing (RNA-seq) at key fetal stages and follow the development of the major cell types as well as populations of transitional cells. We also analyze stem cell (hPSC)-derived retinal organoids; although organoids have a very similar cellular composition at equivalent ages as the fetal retina, there are some differences in gene expression of particular cell types. Moreover, the inner retinal lamination is disrupted at more advanced stages of organoids compared with fetal retina. To determine whether the disorganization in the inner retina is due to the culture conditions, we analyze retinal development in fetal retina maintained under similar conditions. These retinospheres develop for at least 6 months, displaying better inner retinal lamination than retinal organoids. Our single-cell RNA sequencing (scRNA-seq) comparisons of fetal retina, retinal organoids, and retinospheres provide a resource for developing better in vitro models for retinal disease. 2020-02-04 /pmc/articles/PMC7901645/ /pubmed/32023475 http://dx.doi.org/10.1016/j.celrep.2020.01.007 Text en This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Sridhar, Akshayalakshmi
Hoshino, Akina
Finkbeiner, Connor R.
Chitsazan, Alex
Dai, Li
Haugan, Alexandra K.
Eschenbacher, Kayla M.
Jackson, Dana L.
Trapnell, Cole
Bermingham-McDonogh, Olivia
Glass, Ian
Reh, Thomas A.
Single-Cell Transcriptomic Comparison of Human Fetal Retina, hPSC-Derived Retinal Organoids, and Long-Term Retinal Cultures
title Single-Cell Transcriptomic Comparison of Human Fetal Retina, hPSC-Derived Retinal Organoids, and Long-Term Retinal Cultures
title_full Single-Cell Transcriptomic Comparison of Human Fetal Retina, hPSC-Derived Retinal Organoids, and Long-Term Retinal Cultures
title_fullStr Single-Cell Transcriptomic Comparison of Human Fetal Retina, hPSC-Derived Retinal Organoids, and Long-Term Retinal Cultures
title_full_unstemmed Single-Cell Transcriptomic Comparison of Human Fetal Retina, hPSC-Derived Retinal Organoids, and Long-Term Retinal Cultures
title_short Single-Cell Transcriptomic Comparison of Human Fetal Retina, hPSC-Derived Retinal Organoids, and Long-Term Retinal Cultures
title_sort single-cell transcriptomic comparison of human fetal retina, hpsc-derived retinal organoids, and long-term retinal cultures
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7901645/
https://www.ncbi.nlm.nih.gov/pubmed/32023475
http://dx.doi.org/10.1016/j.celrep.2020.01.007
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