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作 者:贾赛雄[1] 利春叶[1] 洪意侠 翁启文 吴迪[1] 龙海泉[1] 陈金仁[1] JIA Sai-xiong;LI Chun-ye;HONG Yi-xia;WENG Qi-wen;WU Di;LONG Hai-quan;CHEN Jin-ren(Department of Upper Limb Microsurgery,Shenzhen Bao’an District People’s Hospital,Shenzhen,Guangdong,518101,China)
机构地区:[1]深圳市宝安区人民医院上肢显微外科,广东省518101 [2]汕头市中医医院创伤骨科,广东省515041
出 处:《中国骨与关节杂志》2024年第3期195-200,共6页Chinese Journal of Bone and Joint
摘 要:目的探讨富血小板纤维蛋白(platelet-rich fibrin,PRF)对体外培养大鼠骺板软骨细胞增殖和分化的影响。方法选取2周龄SD大鼠4只,获取原代骺板细胞后进行培养及鉴定。采集8周龄大鼠全血10 ml,制备PRF。实验分组:对照组在培养基中不加PRF;实验组在培养基底部加入PRF膜。采用CCK-8、划痕实验、硫酸糖胺聚糖含量(glycosaminoglycan,GAG)检测评价在PRF作用下细胞的增殖、迁移、生物学功能活性。结果PRF作用后48 h,CCK-8检测显示实验组增殖率较对照组显著升高,差异有统计学意义(P<0.05)。PRF作用24 h和48 h,划痕实验提示实验组伤口闭合度分别为(81.27±3.02)%、(97.60±0.89)%,较对照组(28.04±4.50)%、(45.68±2.44)%显著升高,对比差异有统计学意义(P<0.05)。实验组PRF作用24 h,与对照组相比GAG含量差异无统计学意义(P>0.05);PRF作用48 h,实验组的GAG含量为(102.45±4.11)μg/ml,与对照组(56.62±4.61)μg/ml相比显著升高,差异有统计学意义(P<0.05)。结论PRF可以促进骺板软骨细胞增殖、分化,还可以促进GAG的产生。Objective To study the effect of platelet-rich fibrin(PRF)on the proliferation and differentiation of rat epiphyseal plate chondrocytes cultured in vitro.Methods Four 2-week-old SD rats were selected,and primary epiphyseal plate cells were obtained and subjected for culture and identification.10 ml whole blood of 8-weekold rats was collected to prepare PRF.PRF was not added in the medium of the control group;PRF membrane was added at the bottom of the medium of the experimental group.CCK-8,scratch experiment and sulfate glycosamine polysaccharide content glycosaminoglycan(GAG)were used to evaluate the proliferation,migration and biological function activity of cells with PRF.Results After 48h of PRF treatment in the experimental group,the CCK-8 test showed a significantly higher proliferation rate compared with the control group(P<0.05).After 24 h and 48 h of PRF treatment,the scratch experiment indicated that the wound closure of experimental group were(81.27±3.02)%,(97.60±0.89)%,which were significantly higher than the control group[(28.04±4.50)%,(45.68±2.44)%](P<0.05).After 24 h of PRF treatment in the experimental group,there was no statistical difference in GAG content compared with the control group(P>0.05).After 48 h of PRF treatment in the experimental group,the GAG content(102.45±4.11)μg/ml was significantly increased than that of the control group(56.62±4.61)μg/ml(P<0.05).Conclusions PRF can promote the proliferation and differentiation of epiphyseal plate chondrocytes and GAG production.
关 键 词:软骨细胞 生长面 富血小板纤维蛋白 细胞增殖 动物实验
分 类 号:R329.2[医药卫生—人体解剖和组织胚胎学]
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