2023
DOI: 10.1016/j.jconrel.2023.04.003
|View full text |Cite
|
Sign up to set email alerts
|

Mesenchymal stem cell exosomes as nanotherapeutics for dry age-related macular degeneration

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1
1

Citation Types

0
4
0

Year Published

2023
2023
2024
2024

Publication Types

Select...
8

Relationship

0
8

Authors

Journals

citations
Cited by 12 publications
(4 citation statements)
references
References 86 publications
0
4
0
Order By: Relevance
“…5 D). They are important genes for retinal antioxidant enzymes and risk genes for dry AMD [ 25 ], and their increased expression represents an increased ability of the retina to resist oxidative damage [ 26 ].
Fig.
…”
Section: Resultsmentioning
confidence: 99%
“…5 D). They are important genes for retinal antioxidant enzymes and risk genes for dry AMD [ 25 ], and their increased expression represents an increased ability of the retina to resist oxidative damage [ 26 ].
Fig.
…”
Section: Resultsmentioning
confidence: 99%
“…Moreover, as previously noted, MSC-EVs can temper neuroinflammation—a prevalent instigator of oxidative stress—potentially lessening oxidative stress intensity through inflammation reduction. For instance, they can exert their effects through various pathways, including the NF-kB signaling pathway ( Yan et al, 2022 ) and the Nrf2/Keap1 signaling pathway ( Tang et al, 2023 ). Additionally, they have the ability to modulate mitochondrial membrane potential and mitigate mitochondrial ROS production ( Xian et al, 2019 ).…”
Section: Role and Application Of Msc-evs In The Pathophysiological Pr...mentioning
confidence: 99%
“…Using an experimental approach with primary polarized RPE cultures under subtoxic oxidative stress conditions, changes in sEV proteins content involved in epithelial barrier integrity have been reported, which include basal-side specific desmosome and hemidesmosome shedding via sEVs [48], which would explain the RPE-impaired outer blood-retinal barrier function that occurs in AMD. Cellular oxidative damage of the RPE cells induced by NaIO3 could be prevented by the administration of sEVs obtained from mesenchymal stem cells [49], that decreased the levels of reactive oxygen species, and upregulated SOD activity by a mechanism that has been ascribed to the up regulation of the expression of the Nrf2 pathway, since Nrf2 inhibitors block this antioxidant effect [49]. Moreover, recent findings indicate that under oxidative conditions, RPE cells upregulate the expression of CYLD-AS1, a long, noncoding mRNA with the ability to modulate the expression of Nrf2 (associated with oxidative stress) and members of the NF-κB pathway, which play a role in inflammation.…”
Section: Extracellular Vesiclesmentioning
confidence: 99%