Transplantation of derivative retinal organoids from chemically induced pluripotent stem cells restored visual function

As an emerging type of pluripotent stem cells, chemically induced pluripotent stem cells (CiPSCs) avoid the risks of genomic disintegration by exogenous DNAs from viruses or plasmids, providing a safer stem cell source. To verify CiPSCs' capacity to differentiate into retinal organoids (ROs), we induced CiPSCs from mouse embryonic fibroblasts by defined small-molecule compounds and successfully differentiated the CiPSCs into three-dimensional ROs, in which all major retinal cell types and retinal genes were in concordance with those in vivo. We transplanted retinal photoreceptors from ROs into the subretinal space of retinal degeneration mouse models and the cells could integrate into the host retina, establish synaptic connections, and significantly improve the visual functions of the murine models. This proof-of-concept study for the first time demonstrated that CiPSCs could differentiate into ROs with a full spectrum of retinal cell types, and provided new insights into chemical approach-based retinal regeneration for degenerative diseases.

Authors

Institutions

Publication Details

Journal
npj Regenerative Medicine
Published
2024-12-27
DOI
https://doi.org/10.1038/s41536-024-00387-7
Citations
8
Primary Topic
Retinal Development and Disorders
Type
article
Field-Weighted Citation Impact
1.87

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Transplantation of derivative retinal organoids from chemically induced pluripotent stem cells restored visual function

Kangxin Jin, Zi‐Bing Jin, Ning Zhao, Xiao Zhang et al.
8 citations
npj Regenerative Medicine
Retinal Development and Disorders
1.87
article

Transplantation of derivative retinal organoids from chemically induced pluripotent stem cells restored visual function

Kangxin Jin, Zi‐Bing Jin, Ning Zhao, Xiao Zhang, Wen Wang, Chang-Jun Zhang
article en
8 citations

Abstract

As an emerging type of pluripotent stem cells, chemically induced pluripotent stem cells (CiPSCs) avoid the risks of genomic disintegration by exogenous DNAs from viruses or plasmids, providing a safer stem cell source. To verify CiPSCs' capacity to differentiate into retinal organoids (ROs), we induced CiPSCs from mouse embryonic fibroblasts by defined small-molecule compounds and successfully differentiated the CiPSCs into three-dimensional ROs, in which all major retinal cell types and retinal genes were in concordance with those in vivo. We transplanted retinal photoreceptors from ROs into the subretinal space of retinal degeneration mouse models and the cells could integrate into the host retina, establish synaptic connections, and significantly improve the visual functions of the murine models. This proof-of-concept study for the first time demonstrated that CiPSCs could differentiate into ROs with a full spectrum of retinal cell types, and provided new insights into chemical approach-based retinal regeneration for degenerative diseases.

npj Regenerative MedicineVol. 9(1)
Beijing Tongren Hospital (CN), Capital Medical University (CN)
National Natural Science Foundation of China, Natural Science Foundation of Beijing Municipality, Beijing Municipal Science and Technology Commission, Major Research Plan, Young Scientists Fund
Openalex Percentile: Top 14%
Retinal Development and Disorders
1.87
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.

Transplantation of derivative retinal organoids from chemically induced pluripotent stem cells restored visual function — Kangxin Jin, Zi‐Bing Jin, et al. · npj Regenerative Medicine (2024) | TGRS Research Map | TGRS