2021
DOI: 10.1016/j.biopha.2021.112118
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Mesenchymal stem cell-derived exosome microRNA as therapy for cardiac ischemic injury

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Cited by 45 publications
(26 citation statements)
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“…In the mouse model, compared with the use of liposomes, exosomes are able to enter cells more effectively with less immune clearance in vivo ( Ferguson and Nguyen, 2016 ; Barile and Vassalli, 2017 ; Liao et al, 2019 ). Exosomes play an important role in cardiovascular function regulation and cardiovascular and cancer therapy ( Li et al, 2021a ; Lim, 2021 ; Nasser et al, 2021 ; Robson, 2021 ). With the development of technology, artificial exosomes have been used to deliver various nanomedicines ( Li et al, 2021b ).…”
Section: Exosomementioning
confidence: 99%
“…In the mouse model, compared with the use of liposomes, exosomes are able to enter cells more effectively with less immune clearance in vivo ( Ferguson and Nguyen, 2016 ; Barile and Vassalli, 2017 ; Liao et al, 2019 ). Exosomes play an important role in cardiovascular function regulation and cardiovascular and cancer therapy ( Li et al, 2021a ; Lim, 2021 ; Nasser et al, 2021 ; Robson, 2021 ). With the development of technology, artificial exosomes have been used to deliver various nanomedicines ( Li et al, 2021b ).…”
Section: Exosomementioning
confidence: 99%
“…MSC release vesicles of various sizes loaded with miRNAs primarily for cell-to-cell communication. Research has shown that MSC-derived exosomes could accumulate in the ischemic myocardial tissue and regulate cell proliferation, apoptosis, inflammation, and angiogenesis [ 51 , 52 ]. Exosomes can be used as drug delivery systems by being loaded with the required miRNAs to the target organ of interest, such as the heart.…”
Section: Msc-derived Exosomes As Therapy In Different Cvdsmentioning
confidence: 99%
“…Nowadays, exosomal miRNAs are regarded as novel biomarkers for cervical cancer prediction and diagnosis [ 131 , 132 ]. Moreover, BMSCs-derived exosomal miR-150–5p can inhibit the apoptosis of cardiomyocytes and improve the cardiac function via targeting Bax [ 133 , 134 ]. In addition, exosomes derived from BMSCs contained higher miR-29 and miR-24 and lower miR-21, miR-34, and miR-378.…”
Section: Conclusion and Future Perspectivesmentioning
confidence: 99%
“…In addition, exosomes derived from BMSCs contained higher miR-29 and miR-24 and lower miR-21, miR-34, and miR-378. These exosomal miRNAs can improve cardiac function by attenuating fibrosis and inflammation in the rat model of myocardial infarction [ 133 , 135 ].Except for MSCs, neurons, microglia and oligodendrocytes, emerging studies also indicate that astrocytes-derived exosomal miR-26a may impact neuronal function and morphology [ 136 ] and infiltrated macrophages after SCI could aggravate BSCB integrity breakdown by delivering exosomal miR-155 through activating the NF-κB pathway [ 137 ]. Nevertheless, it has not been well studied whether exosomes can accurately transfer miRNAs from their parent cells to their target cells, and the functions of regulating post-transcriptional translation and contribution of SCI and TBI are not transparent.…”
Section: Conclusion and Future Perspectivesmentioning
confidence: 99%