F. Rezaei, Maryam Hassan Famian, H. Shafaei, J. S. Rad, L. Roshangar, A. Montaseri
{"title":"Mummy Enhances Chondrocyte Proliferation and the Expression of Extracellular Matrix Components in Monolayer and 3D Culture Conditions","authors":"F. Rezaei, Maryam Hassan Famian, H. Shafaei, J. S. Rad, L. Roshangar, A. Montaseri","doi":"10.36478/rjbsci.2020.33.39","DOIUrl":null,"url":null,"abstract":": To investigate the probable effects of mummy on chondrocyte proliferation and expression of cartilage specific gene. Chondrocytes at the second passage were plated at density of 1×10 6 in monolayer or seeded onto PCL scaffolds. Cells in both conditions were divided into control (received medium) or treated with mummy at concentrations of 500 or 1000 µg mL G 1 for 72 h. The gene expression profile of collagen II, aggrecan, Cartilage Oligomeric Matrix Protein (COMP) and Sox-9 was evaluated using real-time RT-PCR. The ability of mummy to enhance the proliferation of chondrocytes was further evaluated using doubling time. Treatment of chondrocytes with 1000 µg mL G 1 of mummy resulted in a significant increase in expression of Sox-9, COMP and aggrecan genes in both monolayer and 3D culture conditions. Compared to the monolayer cultivated cells, expression of genes in seeded chondrocytes on PCL scaffolds was significantly higher. The highest proliferation rate of chondrocytes was found at a concentration of 1000 µg mL G 1 . The preliminary findings of this study revealed that mummy can be a promoting factor for chondrocyte proliferation and ECM synthesis. The use of mummy at 1000 µg mL G 1","PeriodicalId":21014,"journal":{"name":"Research journal of pharmaceutical, biological and chemical sciences","volume":"51 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2020-05-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Research journal of pharmaceutical, biological and chemical sciences","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.36478/rjbsci.2020.33.39","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
: To investigate the probable effects of mummy on chondrocyte proliferation and expression of cartilage specific gene. Chondrocytes at the second passage were plated at density of 1×10 6 in monolayer or seeded onto PCL scaffolds. Cells in both conditions were divided into control (received medium) or treated with mummy at concentrations of 500 or 1000 µg mL G 1 for 72 h. The gene expression profile of collagen II, aggrecan, Cartilage Oligomeric Matrix Protein (COMP) and Sox-9 was evaluated using real-time RT-PCR. The ability of mummy to enhance the proliferation of chondrocytes was further evaluated using doubling time. Treatment of chondrocytes with 1000 µg mL G 1 of mummy resulted in a significant increase in expression of Sox-9, COMP and aggrecan genes in both monolayer and 3D culture conditions. Compared to the monolayer cultivated cells, expression of genes in seeded chondrocytes on PCL scaffolds was significantly higher. The highest proliferation rate of chondrocytes was found at a concentration of 1000 µg mL G 1 . The preliminary findings of this study revealed that mummy can be a promoting factor for chondrocyte proliferation and ECM synthesis. The use of mummy at 1000 µg mL G 1
目的:探讨木乃伊对软骨细胞增殖及软骨特异性基因表达的影响。将第二次传代的软骨细胞以1×10 6的密度单层或播种到PCL支架上。将两种情况下的细胞分为对照(接受培养基)或500或1000µg mL g1浓度的木乃伊处理72 h。使用实时RT-PCR评估II型胶原蛋白、聚集蛋白、软骨寡聚物基质蛋白(COMP)和Sox-9的基因表达谱。用倍增时间进一步评价木乃伊促进软骨细胞增殖的能力。用1000µg mL g1木乃伊处理软骨细胞,在单层和三维培养条件下,都能显著增加Sox-9、COMP和聚集蛋白基因的表达。与单层培养细胞相比,种子软骨细胞在PCL支架上的基因表达显著增加。在浓度为1000µg mL g1时,软骨细胞增殖率最高。本研究的初步结果显示木乃伊可能是软骨细胞增殖和ECM合成的促进因子。使用妈咪量为1000µg mL g1