UBA2 activates Wnt/β-catenin signaling pathway during protection of R28 retinal precursor cells from hypoxia by extracellular vesicles derived from placental mesenchymal stem cells.


Journal

Stem cell research & therapy
ISSN: 1757-6512
Titre abrégé: Stem Cell Res Ther
Pays: England
ID NLM: 101527581

Informations de publication

Date de publication:
02 10 2020
Historique:
received: 05 06 2020
accepted: 18 09 2020
entrez: 3 10 2020
pubmed: 4 10 2020
medline: 22 6 2021
Statut: epublish

Résumé

Stem cell transplantation has been proposed as an alternative treatment for intractable optic nerve disorders characterized by irrecoverable loss of cells. Mesenchymal stem cells, with varying tissue regeneration and recovery capabilities, are being considered for potential cell therapies. To overcome the limitations of cell therapy, we isolated exosomes from human placenta-derived mesenchymal stem cells (hPMSCs) and investigated their therapeutic effects in R28 cells (retinal precursor cells) exposed to CoCl After 9 h of exposure to CoCl We observed that exosome could significantly recover proliferation damaged by CoCl This study reported that hypoxic damaged expression of regeneration markers in R28 cells was significantly recovered by hPMSC exosomes. We could also demonstrate that UBA2 played a key role in activating the Wnt/β-catenin signaling pathway during protection of hypoxic damaged R28 cells, induced by hPMSC exosomes.

Sections du résumé

BACKGROUND
Stem cell transplantation has been proposed as an alternative treatment for intractable optic nerve disorders characterized by irrecoverable loss of cells. Mesenchymal stem cells, with varying tissue regeneration and recovery capabilities, are being considered for potential cell therapies. To overcome the limitations of cell therapy, we isolated exosomes from human placenta-derived mesenchymal stem cells (hPMSCs) and investigated their therapeutic effects in R28 cells (retinal precursor cells) exposed to CoCl
METHOD
After 9 h of exposure to CoCl
RESULT
We observed that exosome could significantly recover proliferation damaged by CoCl
CONCLUSION
This study reported that hypoxic damaged expression of regeneration markers in R28 cells was significantly recovered by hPMSC exosomes. We could also demonstrate that UBA2 played a key role in activating the Wnt/β-catenin signaling pathway during protection of hypoxic damaged R28 cells, induced by hPMSC exosomes.

Identifiants

pubmed: 33008487
doi: 10.1186/s13287-020-01943-w
pii: 10.1186/s13287-020-01943-w
pmc: PMC7532108
doi:

Substances chimiques

UBA2 protein, human 0
beta Catenin 0
Ubiquitin-Activating Enzymes EC 6.2.1.45

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

428

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Auteurs

Kyungmin Koh (K)

Department of Ophthalmology, CHA Bundang Medical Center, CHA University, Seongnam, Republic of Korea.
Department of Ophthalmology, Kim's Eye Hospital, Konyang University College of Medicine, Seoul, Republic of Korea.

Mira Park (M)

Department of Ophthalmology, CHA Bundang Medical Center, CHA University, Seongnam, Republic of Korea.

Eun Soo Bae (ES)

Department of Ophthalmology, CHA Bundang Medical Center, CHA University, Seongnam, Republic of Korea.

Van-An Duong (VA)

Gachon Institute of Pharmaceutical Sciences, Gachon College of Pharmacy, Gachon University, Incheon, Republic of Korea.

Jong-Moon Park (JM)

Gachon Institute of Pharmaceutical Sciences, Gachon College of Pharmacy, Gachon University, Incheon, Republic of Korea.

Hookeun Lee (H)

Gachon Institute of Pharmaceutical Sciences, Gachon College of Pharmacy, Gachon University, Incheon, Republic of Korea.

Helen Lew (H)

Department of Ophthalmology, CHA Bundang Medical Center, CHA University, Seongnam, Republic of Korea. eye@cha.ac.kr.

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Classifications MeSH