Urine-derived stem cells-extracellular vesicles ameliorate diabetic osteoporosis through HDAC4/HIF-1α/VEGFA axis by delivering microRNA-26a-5p

Critical roles of stem cell-extracellular vesicles (EVs) in the management of osteoporosis have been documented. Here, this study was designed to enlarge the research of the specific effects and underlying mechanism of urine-derived stem cells-EVs (USCs-EVs) on osteoporosis in diabetes rats. Firstly, miR-26a-5p and histone deacetylase 4 (HDAC4) expression in USCs of rats after diabetic osteoporosis (DOP) modeling induced by streptozotocin injection was determined, followed by study of their interaction. Then, USCs-EVs were co-cultured with osteogenic precursor cells, the effects of miRNA-26a-5p (miR-26a-5p) on osteoblasts, osteoclasts, bone mineralization deposition rate were evaluated. Meanwhile, the effect of USCs-EVs carrying miR-26a-5p on DOP rats was assessed. Elevated miR-26a-5p was seen in USCs-EVs which limited HDAC4 expression. Moreover, USCs-EVs delivered miR-26a-5p to osteogenic precursor cells, thereby promoting their differentiation, enhancing the activity of osteoblasts, and inhibiting the activity of osteoclasts, thereby preventing DOP through the activation of hypoxia inducible factor 1 subunit alpha (HIF-1 alpha)/vascular endothelial growth factor A (VEGFA) pathway by repressing HDAC4. In a word, USCs-EVsmiR-26a-5p is a promising therapy for DOP by activating HIF-1 alpha/VEGFA pathway through HDAC4 inhibition.

Automated summary

The specific effects and underlying mechanism of urine-derived stem cells-extracellular vesicles (USCs-EVs) on osteoporosis in diabetes rats were studied. It was found that USCs-EVs carrying miR-26a-5p activated the HIF-1α/VEGFA pathway through HDAC4 inhibition to prevent diabetic osteoporosis (DOP).