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胶原合成介导的软骨细胞的光生物调节作用
引用本文:杨小红,刘承宜,刘少杰,谭见容,梁佩红.胶原合成介导的软骨细胞的光生物调节作用[J].激光生物学报,2007,16(3):266-270.
作者姓名:杨小红  刘承宜  刘少杰  谭见容  梁佩红
作者单位:1. 暨南大学医学院第四附属医院,广州市创伤外科研究所,广东,广州,510220
2. 华南师范大学激光运动医学实验室,广东,广州,510631
基金项目:国家自然科学基金 , 广东省卫生厅科研项目
摘    要:目的:了解低强度激光照射对软骨细胞增殖的影响及其机制。方法:选取3周龄新西兰白兔分离培养软骨细胞,在2.5%新生牛血清中培养,用半导体激光(650 nm,2.96 mW/cm2)(sem iconductor laser irrad iation,SLI)照第4代软骨细胞,每天分别照射1 m in、3 m in、5 m in、7 m in、10 m in、20 m in,共6 d。收集激光照射后第2 d、4 d、6 d、8 d、10 d和12 d的细胞培养液,用氯胺T消化法检测羟脯氨酸(H rp)的含量。在培养至第13 d时,用XTT法检测细胞的活性,了解细胞的增殖情况。结果:在2.5%新生牛血清中,SLI对软骨细胞具有明显的光生物调节作用:(1)在培养至第13 d时,所有剂量组在照射后XTT吸光度值均有不同程度的增高,其中3 m in、5 m in、7 m in和10 m in组的增高较为明显(P<0.01);(2)两因素重复测定资料的方差分析结果显示,SLI照射后软骨细胞合成胶原的能力在逐步增加,而对照组在培养至第2周开始H rp含量明显下降。结论:SLI照射可促进2.5%新生牛血清中兔软骨细胞增殖,这个过程可能是通过促进胶原合成实现的。

关 键 词:半导体激光  光生物调节作用  软骨细胞  胶原  羟脯氨酸
文章编号:1007-7146(2007)03-0266-05
收稿时间:2007-03-15
修稿时间:2007-03-15

Collagen Synthesis Mediated Chondrocyte Photobiomodulation in vitro
YANG Xiao-hong,LIU Cheng-yi,LIU Shao-jie,TAN Jian-rong,LIANG Pei-hong.Collagen Synthesis Mediated Chondrocyte Photobiomodulation in vitro[J].ACTA Laser Biology Sinica,2007,16(3):266-270.
Authors:YANG Xiao-hong  LIU Cheng-yi  LIU Shao-jie  TAN Jian-rong  LIANG Pei-hong
Institution:1. Guangzhou Institute of Traumatology, the 4th Affiliated Hospital of Medical College of Jinan University, Guangzhou 510220, Guangdong, China; 2. Laboratory of Laser Sports Medicine, South China Normal University, Guangzhou 510631, Guangdong, China
Abstract:Objective:the effects of low intensity laser irradiation on the chondrocyte proliferation and its mechanism were studied.Methods: the chondrocytes isolated from the cartilage sample of 3-week-old New Zealand white rabbits were cultured with 10 % newborn calf serum(NCS),irradiated by 650 nm semiconductor laser irradiation(SLI) at 2.96 mW/cm2 for 1 min,3 min,5 min,7 min,10 min and 20 min per day for 6 days,and then incubated till the 13th day at 2.5 % NCS.The type II collagen synthesis was assessed by a hydroxyproline(Hpr) content measurement on the 2nd,4th,6th,8th,10th and 12th day after the first SLI irradiation,respectively.The proliferation on the 13th day was assessed by a XTT assay.Results:There is significant photobiomodulation on the proliferation of the chondrocytes cultured at 2.5 % NCS.(1) The chondrocyte proliferation was significantly(P<0.01) promoted for the groups irradiated by SLI for 3,5,7 and 10 min,respectively,on the 13rd day;(2) The type II collagen synthesis increased steadily with days in the group irradiated by SLI for 5 min.Conclusions: the proliferation of the chondrocyte cultured at 2.5 % NCS might be promoted by SLI,which might be mediated by collagen synthesis.
Keywords:semiconductor laser  photobiomodulation  chondrocytes  collagen  hydroxyproline
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