Evidence map›Paper›PMID 37569444›Full record

ArticleInternational journal of molecular sciences2023

Intravitreal Administration of Retinal Organoids-Derived Exosomes Alleviates Photoreceptor Degeneration in Royal College of Surgeons Rats by Targeting the Mitogen-Activated Protein Kinase Pathway.

Jung Woo Han, Hun Soo Chang, Jin Young Yang, Han Sol Choi, Hyo Song Park, Hyoung Oh Jun, Ji Hye Choi, Sun-Sook Paik, Kyung Hwun Chung, Hee Jeong Shin and 9 more

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.5field-weighted citation impact, top 11% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

16 citing papers in PubMed, 16 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

19 authors at 6 institutions in 2 countries.

Jung Woo HanDepartment of Ophthalmology, Soonchunhyang University Bucheon Hospital, Bucheon 31538, Republic of Korea.
Hun Soo ChangDepartment of Microbiolo and BK21 FOUR Project, Soonchunhyang University College of Medicine, Cheonan 31538, Republic of Korea.
Jin Young YangLaboratory of Molecular Therapy for Retinal Degeneration, Soonchunhyang University Bucheon Hospital, Bucheon 31538, Republic of Korea.
Han Sol ChoiDepartment of Ophthalmology, Soonchunhyang University Bucheon Hospital, Bucheon 31538, Republic of Korea.ORCID 0009-0007-7022-3540
Hyo Song ParkDepartment of Ophthalmology, Soonchunhyang University Bucheon Hospital, Bucheon 31538, Republic of Korea.
Hyoung Oh JunLaboratory of Molecular Therapy for Retinal Degeneration, Soonchunhyang University Bucheon Hospital, Bucheon 31538, Republic of Korea.
Ji Hye ChoiLaboratory of Molecular Therapy for Retinal Degeneration, Soonchunhyang University Bucheon Hospital, Bucheon 31538, Republic of Korea.
Sun-Sook PaikDepartment of Anatomy, College of Medicine, The Catholic University of Korea, Seoul 14662, Republic of Korea.
Kyung Hwun ChungLaboratory of Molecular Therapy for Retinal Degeneration, Soonchunhyang University Bucheon Hospital, Bucheon 31538, Republic of Korea.
Hee Jeong ShinDepartment of Interdisciplinary Program in Biomedical Science, Soonchunhyang Graduate School, Soonchunhyang University Bucheon Hospital, Bucheon 31538, Republic of Korea.ORCID 0000-0002-0944-6637
Seungyeon NamDepartment of Neuroscience and Behavior, University of Notre Dame College of Science, Notre Dame, IN 46556, USA.
Ji-Hye SonDepartment of Microbiolo and BK21 FOUR Project, Soonchunhyang University College of Medicine, Cheonan 31538, Republic of Korea.
Si Hyung LeeDepartment of Ophthalmology, Soonchunhyang University Bucheon Hospital, Bucheon 31538, Republic of Korea.
Eun Jung LeeDepartment of Biological Sciences and KAIST Stem Cell Center, Korea Advanced Institute of Science and Technology, Daejeon 34141, Republic of Korea.ORCID 0000-0001-5145-4449
Kyoung Yul SeoDepartment of Ophthalmology, Severance Hospital, Institute of Vision Research, Yonsei University College of Medicine, Seoul 03722, Republic of Korea.ORCID 0000-0002-9855-1980
Jungmook LyuDepartment of Medical Science, Konyang University, Daejun 32992, Republic of Korea.
Jin Woo KimDepartment of Biological Sciences and KAIST Stem Cell Center, Korea Advanced Institute of Science and Technology, Daejeon 34141, Republic of Korea.ORCID 0000-0003-0767-1918
In-Beom KimDepartment of Anatomy, College of Medicine, The Catholic University of Korea, Seoul 14662, Republic of Korea.ORCID 0000-0002-1932-8407
Tae Kwann ParkDepartment of Ophthalmology, Soonchunhyang University Bucheon Hospital, Bucheon 31538, Republic of Korea.ORCID 0000-0001-9689-4384
Soonchunhyang University · KRCatholic University of Korea · KRKorea Advanced Institute of Science and Technology · KRKonyang University · KRUniversity of Notre Dame · USYonsei University · KR

Funding

Soonchunhyang University research fundthe grant of Technology Innovation Program 20009844the Ministry of Health & Welfare, Republic of Korea HI21C0317the Ministry of Trade, Industry & Energy
6 · The paper itself

Abstract

Increasing evidence suggests that exosomes are involved in retinal cell degeneration, including their insufficient release; hence, they have become important indicators of retinopathies. The exosomal microRNA (miRNA), in particular, play important roles in regulating ocular and retinal cell functions, including photoreceptor maturation, maintenance, and visual function. Here, we generated retinal organoids (ROs) from human induced pluripotent stem cells that differentiated in a conditioned medium for 60 days, after which exosomes were extracted from ROs (Exo-ROs). Subsequently, we intravitreally injected the Exo-RO solution into the eyes of the Royal College of Surgeons (RCS) rats. Intravitreal Exo-RO administration reduced photoreceptor apoptosis, prevented outer nuclear layer thinning, and preserved visual function in RCS rats. RNA sequencing and miRNA profiling showed that exosomal miRNAs are mainly involved in the mitogen-activated protein kinase (MAPK) signaling pathway. In addition, the expression of MAPK-related genes and proteins was significantly decreased in the Exo-RO-treated group. These results suggest that Exo-ROs may be a potentially novel strategy for delaying retinal degeneration by targeting the MAPK signaling pathway.

Indexed as

ExosomesInduced Pluripotent Stem CellsMicroRNAsRetinal DegenerationSurgeonsAnimalsHumansMitogen-Activated Protein KinasesRatsReactive Oxygen SpeciesMicroRNAsMitogen-Activated Protein KinasesReactive Oxygen Speciesexosomesextracellular vesiclesMAPK pathway signalingretinal degenerationretinal organoids

Identifiers

PMID37569444
PMCPMC10419150
OpenAlexW4385346716

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.