Exosomes isolated from melatonin-stimulated mesenchymal stem cells improve kidney function by regulating inflammation and fibrosis in a chronic kidney disease mouse model.
Ji-Hye YeaYeo Min YoonJun Hee LeeChul Won YunSang Hun LeePublished in: Journal of tissue engineering (2021)
Chronic kidney disease (CKD) is defined as structural and functional abnormalities of the kidney due to inflammation and fibrosis. We investigated the therapeutic effects of exosomes secreted by melatonin-stimulated mesenchymal stem cells (Exocue) on the functional recovery of the kidney in a CKD mouse model. Exocue upregulated gene expression of micro RNAs (miRNAs) associated with anti-inflammatory and anti-fibrotic effects. Exocue-treated groups exhibited low tumor necrosis factor-α and transforming growth factor-β levels in serum and fibrosis inhibition in kidney tissues mediated through regulation of cell apoptosis and proliferation of fibrosis-related cells. Exocue treatment decreased the gene expression of CKD progression-related miRNAs. Moreover, the CKD severity was alleviated in the Exocue group via upregulation of aquaporin 2 and 5 levels and reduction of blood urea nitrogen and creatinine, resulting in functional recovery of the kidney. In conclusion, Exocue could be a novel therapeutic agent for treating CKD by regulating inflammation and fibrosis.
Keyphrases
- chronic kidney disease
- mesenchymal stem cells
- gene expression
- end stage renal disease
- mouse model
- transforming growth factor
- oxidative stress
- umbilical cord
- dna methylation
- stem cells
- anti inflammatory
- epithelial mesenchymal transition
- bone marrow
- liver fibrosis
- cell proliferation
- signaling pathway
- induced apoptosis
- rheumatoid arthritis
- metabolic syndrome
- poor prognosis
- high resolution