2019
DOI: 10.1016/j.jconrel.2019.11.003
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Injectable extracellular vesicle-released self-assembling peptide nanofiber hydrogel as an enhanced cell-free therapy for tissue regeneration

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Cited by 113 publications
(76 citation statements)
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“…Moreover, proliferation of endothelial cells and angiogenesis were both improved, resulting in reduced chronic renal fibrosis. [135] The angiogenesis-enhancing properties of MSC-EVs have already been demonstrated in vivo, and the administration of MSC-EVs incorporated in matrigel enhanced the angiogenesis even more, due to the sustained release and prolonged residence of the EVs. [200] Age-induced vascular dysfunction was treated with umbilical cord mesenchymal stem cell-derived exosomes (UMSCs-exos) containing miR-675 and encapsulated in silk fibroin hydrogels, in order to be delivered into the ischemic hind-limb of mice.…”
Section: Extracellular Vesiclesmentioning
confidence: 99%
“…Moreover, proliferation of endothelial cells and angiogenesis were both improved, resulting in reduced chronic renal fibrosis. [135] The angiogenesis-enhancing properties of MSC-EVs have already been demonstrated in vivo, and the administration of MSC-EVs incorporated in matrigel enhanced the angiogenesis even more, due to the sustained release and prolonged residence of the EVs. [200] Age-induced vascular dysfunction was treated with umbilical cord mesenchymal stem cell-derived exosomes (UMSCs-exos) containing miR-675 and encapsulated in silk fibroin hydrogels, in order to be delivered into the ischemic hind-limb of mice.…”
Section: Extracellular Vesiclesmentioning
confidence: 99%
“…Considering the mechanism responsible for this in vitro in cisplatin-treated human tubular epithelial cells, it was shown that the EVs up-regulated anti-apoptotic genes (B-cell lymphoma extra-large B-cell lymphoma 2 and baculoviral IAP repeat containing 8) and down-regulated genes that contribute in the execution-phase of cell apoptosis (caspase-1, caspase-8 and lymphotoxin alpha) [116]. A significant better EV efficacy followed by improved renal function was noticed when mice BMMSC-EVs were loaded to self-assembling peptide nanofiber hydrogels, for control and targeted release of EVs on the site of mice AKI models after ischaemia-reperfusion [117]. Aside from bone marrow, MSC-EVs from other tissues have been isolated and evaluated for renal regeneration.…”
Section: Kidney Regenerationmentioning
confidence: 99%
“…EVs from various sources have therapeutic potency, among which MSC-derived EVs appear particularly useful in the treatment of diverse conditions, including the treatment of inflammatory disorders of the respiratory system 95 - 98 , heart 99 - 101 , liver 102 - 104 , kidney 105 - 108 , nervous system 109 - 113 , arthrosis 114 - 116 , muscle 117 - 119 and others 120 - 124 ( Table 1 ). The therapeutic action of MSC-EVs is reliant on their transfer of genetic materials and proteins.…”
Section: Applying Ev-based Nanotherapeutics In the Fight Against Inflmentioning
confidence: 99%