Title : Exosomes derived from atorvastatin-pretreated MSC accelerate diabetic wound repair by enhancing angiogenesis via AKT/eNOS pathway.

Pub. Date : 2020 Aug 12

PMID : 32787917






5 Functional Relationships(s)
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1 Exosomes derived from atorvastatin-pretreated MSC accelerate diabetic wound repair by enhancing angiogenesis via AKT/eNOS pathway. Atorvastatin nitric oxide synthase 3 Rattus norvegicus
2 The role of miRNAs and AKT/eNOS signaling pathway in the promoted angiogenesis of ATV-Exos were assessed with their inhibitors. Atorvastatin nitric oxide synthase 3 Rattus norvegicus
3 And AKT/eNOS pathway was activated by ATV-Exos and the pro-angiogenic effects of ATV-Exo were attenuated after the pathway being blocked. Atorvastatin nitric oxide synthase 3 Rattus norvegicus
4 And AKT/eNOS pathway was activated by ATV-Exos and the pro-angiogenic effects of ATV-Exo were attenuated after the pathway being blocked. Atorvastatin nitric oxide synthase 3 Rattus norvegicus
5 CONCLUSIONS: Exosomes originated from ATV-pretreated MSCs might serve as a potential strategy for the treatment of diabetic skin defects through enhancing the biological function of endothelial cells via AKT/eNOS pathway by upregulating the miR-221-3p. Atorvastatin nitric oxide synthase 3 Rattus norvegicus