S. Soleimani, H. Nazem, M. Fazilati, Mohammad Pezeshki Modarres, Seyed Mohammad Atyabi
{"title":"利用滑液和冷大气层等离子体处理纳米纤维pcl基质观察间充质干细胞向软骨细胞的分化","authors":"S. Soleimani, H. Nazem, M. Fazilati, Mohammad Pezeshki Modarres, Seyed Mohammad Atyabi","doi":"10.15406/mojbm.2021.06.00129","DOIUrl":null,"url":null,"abstract":"Tissue engineering has developed strategy for the repair and regeneration of a variety of tissues. The demand for effective treatment strategies of cartilage cause to autologous human Mesenchymal stem cells (hMSC) used for the repair of cartilage defects. In this study effect of some factors on human MSCs for differentiation to chondrocyte were surveyed such as Present of Poly Ɛ-caprolactone (PCL) nanofibrous scaffold and cold atmospheric plasma (CAP), also effect and amount of synovial fluid were evaluated. In this experimental study cell culture for differentiation assay performed in 6 well pellets by DMEM high glucose medium with a supplement of 10% FBS and synovial fluid 5% and 10% of medium add to pellets for 21 days. Total cellular RNA extracted was used for analysis by RT-PCR. Alcian blue staining confirmed the chondrogenic differentiation. MTT assay results in this study showed that the cells proliferation gradually increased from 1st day to 21st days on the electrospun nanofibrous scaffold. Cellular attachment and proliferation of hMSCs showed higher rate on PCL substrate, modified with Helium cold atmospheric plasma, compared to the unmodified and control group at the first day to 21st days. Chondrogenic differentiation confirmed by alcian blue staining, and show high degree of conversion to the chondrocyte. MTT assay and the expression of chondrogenic specific genes Collagen type П and Has-2 in comparison with control groups demonstrated cell survival ability, proliferation and cell differentiation by synovial fluid.","PeriodicalId":127077,"journal":{"name":"MOJ Biology and Medicine","volume":"3 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"1900-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Survey differentiation of mesenchymal stem cell to chondrocyte using synovial fluid and coldatmospheric plasma treated nanofibrous pcl substrate\",\"authors\":\"S. Soleimani, H. Nazem, M. Fazilati, Mohammad Pezeshki Modarres, Seyed Mohammad Atyabi\",\"doi\":\"10.15406/mojbm.2021.06.00129\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Tissue engineering has developed strategy for the repair and regeneration of a variety of tissues. The demand for effective treatment strategies of cartilage cause to autologous human Mesenchymal stem cells (hMSC) used for the repair of cartilage defects. In this study effect of some factors on human MSCs for differentiation to chondrocyte were surveyed such as Present of Poly Ɛ-caprolactone (PCL) nanofibrous scaffold and cold atmospheric plasma (CAP), also effect and amount of synovial fluid were evaluated. In this experimental study cell culture for differentiation assay performed in 6 well pellets by DMEM high glucose medium with a supplement of 10% FBS and synovial fluid 5% and 10% of medium add to pellets for 21 days. Total cellular RNA extracted was used for analysis by RT-PCR. Alcian blue staining confirmed the chondrogenic differentiation. MTT assay results in this study showed that the cells proliferation gradually increased from 1st day to 21st days on the electrospun nanofibrous scaffold. Cellular attachment and proliferation of hMSCs showed higher rate on PCL substrate, modified with Helium cold atmospheric plasma, compared to the unmodified and control group at the first day to 21st days. Chondrogenic differentiation confirmed by alcian blue staining, and show high degree of conversion to the chondrocyte. 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引用次数: 0
摘要
组织工程已经为各种组织的修复和再生制定了策略。自体人间充质干细胞(hMSC)用于软骨缺损的修复需要有效的软骨治疗策略。本研究考察了聚纳米纤维支架(Present of Poly Ɛ-caprolactone, PCL)和冷大气等离子体(cold atmospheric plasma, CAP)等因子对人间充质干细胞向软骨细胞分化的影响,并对滑液的作用和用量进行了评价。本实验采用DMEM高糖培养基,在6孔微球中添加10%胎牛血清和5%滑液,并在微球中添加10%培养基,培养细胞21天。提取细胞总RNA进行RT-PCR分析。阿利新蓝染色证实软骨分化。本研究的MTT实验结果显示,细胞在静电纺纳米纤维支架上的增殖从第1天到第21天逐渐增加。第1 ~ 21天,经氦冷常压等离子体修饰的PCL底物上hMSCs的细胞附着和增殖率高于未修饰的PCL底物和对照组。阿利新蓝染色证实软骨细胞分化,并显示高度转化为软骨细胞。与对照组相比,MTT试验和软骨形成特异性基因Collagen type П和Has-2的表达显示了滑膜液作用下细胞的存活能力、增殖能力和细胞分化能力。
Survey differentiation of mesenchymal stem cell to chondrocyte using synovial fluid and coldatmospheric plasma treated nanofibrous pcl substrate
Tissue engineering has developed strategy for the repair and regeneration of a variety of tissues. The demand for effective treatment strategies of cartilage cause to autologous human Mesenchymal stem cells (hMSC) used for the repair of cartilage defects. In this study effect of some factors on human MSCs for differentiation to chondrocyte were surveyed such as Present of Poly Ɛ-caprolactone (PCL) nanofibrous scaffold and cold atmospheric plasma (CAP), also effect and amount of synovial fluid were evaluated. In this experimental study cell culture for differentiation assay performed in 6 well pellets by DMEM high glucose medium with a supplement of 10% FBS and synovial fluid 5% and 10% of medium add to pellets for 21 days. Total cellular RNA extracted was used for analysis by RT-PCR. Alcian blue staining confirmed the chondrogenic differentiation. MTT assay results in this study showed that the cells proliferation gradually increased from 1st day to 21st days on the electrospun nanofibrous scaffold. Cellular attachment and proliferation of hMSCs showed higher rate on PCL substrate, modified with Helium cold atmospheric plasma, compared to the unmodified and control group at the first day to 21st days. Chondrogenic differentiation confirmed by alcian blue staining, and show high degree of conversion to the chondrocyte. MTT assay and the expression of chondrogenic specific genes Collagen type П and Has-2 in comparison with control groups demonstrated cell survival ability, proliferation and cell differentiation by synovial fluid.