2022
DOI: 10.1038/s41434-021-00310-5
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Exosomal microRNA-133b-3p from bone marrow mesenchymal stem cells inhibits angiogenesis and oxidative stress via FBN1 repression in diabetic retinopathy

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Cited by 21 publications
(14 citation statements)
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“…The miRNAs described above can commonly inhibit angiogenesis through downregulation of target genes. In fact, miR-205 downregulates VEGA in gastric cancer [ 71 ], hepatocellular carcinoma [ 72 ], and the extracellular vesicles from diabetic ulcers [ 73 ], whereas miR133b in the exosomes secreted from bone marrow mesenchymal stem cells downregulates FBN1 [ 74 ] and miR-27b downregulates AMPK in brain microvascular endothelial cells [ 75 ], CDH5 (a.k.a. VE-cadherin) in ovarian cancer [ 76 ], and VEGFC in gastric cancer [ 77 ].…”
Section: Micrornas Related To Cleft Lipmentioning
confidence: 99%
“…The miRNAs described above can commonly inhibit angiogenesis through downregulation of target genes. In fact, miR-205 downregulates VEGA in gastric cancer [ 71 ], hepatocellular carcinoma [ 72 ], and the extracellular vesicles from diabetic ulcers [ 73 ], whereas miR133b in the exosomes secreted from bone marrow mesenchymal stem cells downregulates FBN1 [ 74 ] and miR-27b downregulates AMPK in brain microvascular endothelial cells [ 75 ], CDH5 (a.k.a. VE-cadherin) in ovarian cancer [ 76 ], and VEGFC in gastric cancer [ 77 ].…”
Section: Micrornas Related To Cleft Lipmentioning
confidence: 99%
“…MiR-133b has been described as an anti-angiomiR in murine models of diabetic retinopathy, in which treatment of retinal microvascular endothelial cells with upregulation of miR-133b resulted in impaired proliferation and migration with upregulation of apoptosis ( 155 ). Zhong et al ( 156 ) examined the relationship between miR-133b and EGFR after confirming EGFR as a direct target of miR-133b via luciferase assay and observing downregulation of EGFR in high glucose-treated HUVECs.…”
Section: Dysregulated Micrornas In Diabetic Angiogenesismentioning
confidence: 99%
“…Furthermore, EVs can themselves be therapeutic or serve as delivery vehicles for encapsulated therapeutic molecules (drugs, peptides, small molecules) and notably both of these approaches have been utilized for several eye diseases including specific retinal disease (Table 3). (Aboul Naga et al, 2015;Moisseiev et al, 2017;Zhu et al, 2017;Zhou et al, 2018;Xu et al, 2019;Bian et al, 2020;Kang et al, 2020;Dong et al, 2021;Gu et al, 2021;Tian et al, 2021;Wang T et al, 2021;Wang W et al, 2021;Zhou et al, 2021;Liang et al, 2022;Lin et al, 2022;Liu Y et al, 2022;Pollalis et al, 2022;Ren et al, 2022;Zhou et al, 2022) To date, two different modes of encapsulating molecules, active and passive, have been used with EVs. Active encapsulation includes sonication of drugs or molecules in the cells.…”
Section: Ev-based Therapeutics For Retinal Diseasesmentioning
confidence: 99%
“…Mechanistically, this was due to the internalization of mNPC-exosomes by the retinal microglia, which suppressed their activation. Recently, bone marrow mesenchymal stem cell (BMSC)-derived exosomal miR-133b-3p suppressed angiogenesis and oxidative stress in a mouse model of DR ( Liang et al, 2022 ). Furthermore, BMSC-derived exosomes co-cultured with high glucose-treated Muller glial cells inhibited oxidative stress, inflammation, apoptosis, and promoted cell proliferation in a DR model ( Li W et al, 2021 ).…”
Section: Ev-based Therapeutics For Retinal Diseasesmentioning
confidence: 99%