2022
DOI: 10.1007/s12012-022-09743-9
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Mesenchymal Stem Cell-Derived Exosome-Loaded microRNA-129-5p Inhibits TRAF3 Expression to Alleviate Apoptosis and Oxidative Stress in Heart Failure

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Cited by 28 publications
(14 citation statements)
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“…Several signaling pathways has been proved to regulate oxidative stress in HF, like Nrf2/HO-1/Ca2 + -SERCA2a axis ( 42 ), phosphoinositide 3-kinase/protein kinase B (PI3K/Akt) pathway ( 43 ), and IL-6/STAT3 ( 44 ). Mesenchymal stem cell derived exosomes could inhibit oxidative stress, inflammation and cell apoptosis via inhibiting inflammatory related NF-κB pathway in HF ( 45 ). In chronic HF, the level of inflammation is associated with oxidative stress.…”
Section: Discussionmentioning
confidence: 99%
“…Several signaling pathways has been proved to regulate oxidative stress in HF, like Nrf2/HO-1/Ca2 + -SERCA2a axis ( 42 ), phosphoinositide 3-kinase/protein kinase B (PI3K/Akt) pathway ( 43 ), and IL-6/STAT3 ( 44 ). Mesenchymal stem cell derived exosomes could inhibit oxidative stress, inflammation and cell apoptosis via inhibiting inflammatory related NF-κB pathway in HF ( 45 ). In chronic HF, the level of inflammation is associated with oxidative stress.…”
Section: Discussionmentioning
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%
“…In this study, miR-182 shuttling by sEVs targets Toll-like receptor 4 (TLR4), the inhibition of which leads to anti-inflammatory M2 macrophage conversion ( Vergadi et al, 2017 ), thus promoting macrophage polarization and alleviating inflammation. Similarly, another study showed that in an ischemia-induced mouse heart failure model, sEVs derived from BMMSCs improved cardiac function by inhibiting NF-κB signaling, a transcription factor for cytokine release, and miR-129-5p carried by sEVs was proven to target tumor necrosis factor receptor-associated factor 3 (TRAF3), which subsequently regulates NF-kB ( Yan et al, 2022 ). The anti-inflammatory effects of sEVs derived from BMMSCs were not only found in ischemic heart injury, doxorubicin-induced heart failure models and sepsis-induced heart failure models but also significantly reduced inflammatory factor release when BMMSC-derived sEVs are injected into hearts ( Wang et al, 2015 ; Sun et al, 2018 ; Pei et al, 2021 ).…”
Section: Anti-inflammatory Actions Of Bmmsc-sevs On Ihdmentioning
confidence: 99%