激光生物学报摘要, 更新时间: 2007年10月13日
  由美国生科集团 (BVTech, Inc.) 主办
  
胶原合成介导的软骨细胞的光生物调节作用
激光生物学报摘要 2007-3

杨小红1 , 刘承宜2 , 刘少杰1 , 谭见容1 , 梁佩红1 (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)

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)(semiconductor laser irradiation, SLI)照第4代软骨细胞后,每天分别照射1 min、3 min、5 min、7 min、10 min、20 min,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(Hrp)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 min、5 min、7 min和10 min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Hrp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。


Collagen Synthesis Mediated Chondrocyte Photobiomodulation in Vitro

YANG Xiao-Hong1, LIU Timon Cheng-Yi2, LIU Shao-Jie1, TAN Jian-Rong1, LIANG Pie-Hong1. ( 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 650nm 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.


 

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