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硫酸软骨素纳米硒可抑制T-2毒素诱导的大骨节病软骨细胞凋亡
引用本文:韩晶,郭雄,吴翠艳,李春燕,何淑兰,段琛,宁玉洁. 硫酸软骨素纳米硒可抑制T-2毒素诱导的大骨节病软骨细胞凋亡[J]. 南方医科大学学报, 2013, 33(2): 225-229
作者姓名:韩晶  郭雄  吴翠艳  李春燕  何淑兰  段琛  宁玉洁
作者单位:西安交通大学医学院公共卫生系地方病研究所//环境与疾病相关基因教育部重点实验室,陕西西安,710061
基金项目:国家自然科学基重点项目
摘    要:目的确定硫酸软骨素纳米硒对T-2毒素干预体外大骨节病软骨细胞生长的影响。方法合成并表征硫酸软骨素纳米硒粒
子,依据《大骨节病临床诊断标准》(WS/T 207-2010),选择Ⅱ/Ⅲ度KBD患者6例关节软骨进行体外分离、培养。分别给予硫酸
软骨素纳米硒联合T-2毒素进行干预,采用MTT、HE染色和流式细胞仪观察细胞生长和凋亡的变化。结果合成的硫酸软骨素
纳米硒中硒的含量为10.1%,可在蒸馏水中自组装成粒径为30~200 nm纳米粒子,红外图谱提示纳米硒与硫酸软骨素可能以共
价键的方式结合;硫酸软骨素纳米硒在浓度为50~200 ng/ml可有效抑制20 ng/ml T-2毒素诱导大骨节病软骨细胞的凋亡作用,
降低T-2毒素诱导软骨细胞的早期凋亡率[(8.64±1.57)%,P<0.05]。结论硫酸软骨素纳米硒具有抗T-2毒素诱导软骨细胞凋亡
的作用,可作为一种潜在的治疗大骨节病的药物制剂。


关 键 词:大骨节病  软骨细胞  硫酸软骨素纳米硒  T-2毒素  细胞凋亡

Nano-Se-chondroitin sulfate inhibits T-2 toxin-induced apoptosis of cultured chondrocytes from patients with Kashin-Beck disease
HAN Jing , GUO Xiong , WU Cuiyan , LI Chunyan , HE Shulan , DUAN Chen , NING Yujie. Nano-Se-chondroitin sulfate inhibits T-2 toxin-induced apoptosis of cultured chondrocytes from patients with Kashin-Beck disease[J]. Journal of Southern Medical University, 2013, 33(2): 225-229
Authors:HAN Jing    GUO Xiong    WU Cuiyan    LI Chunyan    HE Shulan    DUAN Chen    NING Yujie
Affiliation:Institute of Endemic Diseases,Faculty of Public Health,Xi’an Jiaotong University College of Medicine/Key Laboratory of Environment and Gene Related to Diseases of Ministry Education,Xi’an 710061,China
Abstract:Objective To observe the effect of nano-Se-chondroitin sulfate on the growth and apoptosis of chondrocytes from
patients with Kashin-Beck disease (KBD) exposed to T-2 toxin in vitro. Methods Samples of the articular cartilage were
obtained from 6 patients with grade II/III KBD diagnosed in line with the National Clinical Diagnostic Criteria of KBD (WS/T
207-2010) for chondrocyte separation and culture in vitro. The separated chondrocytes were treated with synthesized
nano-Se-chondroitin sulfate particles and T-2 toxin, alone or in combination, and the cell growth and apoptosis were observed
using MTT assay, HE staining and flow cytometry. Results The synthesized nano-Se-chondroitin sulfate, with a selenium
entrapment ratio of 10.1%, spontaneously formed nanoparticles in distilled water with sizes ranging from 30 to 200 nm.
Fourier-transform infrared spectroscopy suggested a possible covalent bond that bound Nano-Se and chondroitin sulfate.
Within the concentration range of 50-200 ng/ml, nano-Se-chondroitin sulfate significantly inhibited T-2 toxin-induced
apoptosis of the cultured chondrocytes and reduced the early apoptosis rate to (8.64±1.57)% (P<0.05). Conclusion Nano-Sechondroitin
sulfate can inhibit T-2 toxin-induced apoptosis of cultured chondrocytes from KBD patients in vitro, and serves as
a promising candidate therapeutic agent for KBD.
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