BACKGROUND:Traditional methods of urinary tract reconstruction are limited by donor scarcity,high complication rates,and suboptimal functional recovery.Tissue engineering strategies offer new directions in this field.Since the urinary tract is mainly composed of muscle tissue,the key is to find suitable seed cells and efficiently induce them to differentiate into smooth muscle cells.Comparative studies on the efficacy of different smooth muscle cell induction regimens are still lacking. OBJECTIVE:To isolate,culture,and identify human urine-derived stem cells,and to compare the effects of two different induction protocols. METHODS:Human urine-derived stem cells were isolated from urine samples of 11 healthy adult volunteers by multiple centrifugations.Surface markers were identified by flow cytometry.The multi-directional differentiation potential of human urine-derived stem cells was verified through osteogenic and adipogenic differentiation.Differentiation was induced by transforming growth factor-β1 or transforming growth factor-β1 combined with platelet derived growth factor for 14 days.Immunofluorescence staining and western blot assay were employed to compare the expression differences of smooth muscle-specific proteins(α-SMA and SM22). RESULTS AND CONCLUSION:(1)Urine-derived stem cells were successfully isolated from the eight urine samples of healthy people.These cells exhibit a"rice grain"-like morphology and possess a robust proliferative capacity.(2)Urine-derived stem cells exhibited high expression of mesenchymal stem cell surface markers(CD73,CD90,and CD44)and extremely low expression of hematopoietic stem cell surface markers(CD34 and CD45).These cells did not express CD19,CD105,and HLA-DR.(3)After osteogenic and adipogenic differentiation,the formation of calcium nodules and lipid droplets was observed,with positive staining results from Alizarin Red S and Oil Red O staining.(4)After 14 days of smooth muscle induction culture,immunofluorescence staining revealed that the smooth muscle differentiation rate of urine-derived stem cells treated with a combination of transforming growth factor-β1 and platelet derived growth factor was significantly higher compared to those treated with transforming growth factor-β1 alone(P<0.005).(5)After 14 days of smooth muscle induction culture,western blot assay further demonstrated that the expression levels of α-SMA and SM22 in the transforming growth factor-β1/platelet derived growth factor group were significantly elevated compared to those in the transforming growth factor-β1 only group(P<0.005).These findings confirm that urine-derived stem cells can be non-invasively isolated using multiple rounds of centrifugation.Compared with transforming growth factor-β1 alone,the combination of transforming growth factor-β1 and platelet derived growth factor can improve the efficiency of inducing urine-derived stem cells to differentiate into smooth muscle cells.

The aim of this study is to investigate the effect of Mito TEMPO on the preservation of porcine semen in liquid form.The preservation solution was supplemented with 0,0.5,5.0,50.0,and 500.0 μmol/L of Mito TEMPO,and the diluted boar semen was stored at 17 ℃ for 1 to 5 days.After preservation,we measured sperm motility,acrosome integrity,plasma membrane integrity,reactive oxygen species(ROS)content,total antioxidant capacity,and mitochondrial membrane potential.The fertilization ability and embryonic development potential of sperm preserved for 5 days were assessed using an in vitro fertilization test.The results indicated that the addition of 5.0,50.0 μmol/L of Mito TEMPO to the preservation solution significantly reduced ROS content and improved sperm motility,plasma membrane integrity,acrosome integrity,mitochondrial membrane potential,and antioxidant capacity.Furthermore,it enhanced the fertilization and embryonic devel-opment potential of the preserved sperm.Therefore,Mito TEMPO is beneficial for the preservation of porcine semen in liquid form and may serve as a foundation for the development of liquid semen preservation solutions.

The aim of this study is to investigate the effect of Mito TEMPO on the preservation of porcine semen in liquid form.The preservation solution was supplemented with 0,0.5,5.0,50.0,and 500.0 μmol/L of Mito TEMPO,and the diluted boar semen was stored at 17 ℃ for 1 to 5 days.After preservation,we measured sperm motility,acrosome integrity,plasma membrane integrity,reactive oxygen species(ROS)content,total antioxidant capacity,and mitochondrial membrane potential.The fertilization ability and embryonic development potential of sperm preserved for 5 days were assessed using an in vitro fertilization test.The results indicated that the addition of 5.0,50.0 μmol/L of Mito TEMPO to the preservation solution significantly reduced ROS content and improved sperm motility,plasma membrane integrity,acrosome integrity,mitochondrial membrane potential,and antioxidant capacity.Furthermore,it enhanced the fertilization and embryonic devel-opment potential of the preserved sperm.Therefore,Mito TEMPO is beneficial for the preservation of porcine semen in liquid form and may serve as a foundation for the development of liquid semen preservation solutions.