流式细胞术
琼脂糖凝胶电泳
细胞凋亡
壳聚糖
MTT法
细胞周期
DNA断裂
细胞生长
细胞培养
化学
分子生物学
生物
生物化学
程序性细胞死亡
DNA
遗传学
作者
Lifeng Qi,Zirong Xu,Yan Li,Xia Jiang,Xinyan Han
出处
期刊:PubMed
[National Institutes of Health]
日期:2005-09-07
卷期号:11 (33): 5136-41
被引量:161
标识
DOI:10.3748/wjg.v11.i33.5136
摘要
AIM: To investigate the effects of chitosan nanoparticles on proliferation of human gastric carcinoma cell line MGC803 in vitro and the possible mechanisms involved. METHODS: Chitosan nanoparticles were characterized by particle size, zeta potential, and morphology. After treatment with various concentrations of chitosan nanoparticles (25, 50, 75, 100 microg/mL) at various time intervals, cell proliferation, ultrastructural changes, DNA fragmentation, mitochondrial membrane potential (MMP), cell cycle phase distribution and apoptotic peaks of MGC803 cells were analyzed by MTT assay, electron microscopy, DNA agarose gel electrophoresis, and flow cytometry. RESULTS: Chitosan nanoparticles exhibited a small particle size as 65 nm and a high surface charge as 52 mV. Chitosan nanoparticles markedly inhibited cell proliferation of MGC803 cells with an IC50 value of 5.3 microg/mL 48 h after treatment. After treatment with chitosan nanoparticles, the typical necrotic cell morphology was observed by electron microscopy, a typical DNA degradation associated with necrosis was determined by DNA agarose electrophoresis. Flow cytometry showed the loss of MMP and occurrence of apoptosis in chitosan nanoparticles-treated cells. CONCLUSION: Chitosan nanoparticles effectively inhibit the proliferation of human gastric carcinoma cell line MGC803 in vitro through multiple mechanisms, and may be a beneficial agent against human carcinoma.
科研通智能强力驱动
Strongly Powered by AbleSci AI