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作 者:张玲玲[1] 范晓云[1] 吴莎莎[1] 王亚妮[1]
机构地区:[1]安徽医科大学第一附属医院老年医学呼吸内科,合肥230022
出 处:《临床与实验病理学杂志》2016年第10期1135-1139,共5页Chinese Journal of Clinical and Experimental Pathology
基 金:国家自然科学基金青年科学基金(81100027);安徽省高校省级自然科学研究项目(KJ2011A176);2016年高校学科(专业)拔尖人才学术资助重点项目(gxbj ZD2016036);安徽人社厅第九批学术和技术带头人及后备人选学术科研活动资助
摘 要:目的观察多聚左旋精氨酸(poly-L-arginine,PLA)诱导气道上皮细胞NCI-H292凋亡以及对细胞内BCL-2/Bax、Caspase 3表达的影响,从而揭示PLA参与哮喘气道损伤的机制。方法按PLA浓度不同分为对照组、10 mg/L组、20 mg/L组、40 mg/L组、60 mg/L组,流式细胞仪检测各组PLA作用24 h后NCI-H292细胞凋亡率;电镜下观察60 mg/L组PLA作用24 h后NCIH292细胞凋亡形态学改变;Western blot法检测各组PLA作用24 h后NCI-H292细胞内Bax、BCL-2及活性Caspase 3的表达。结果各组NCI-H292细胞凋亡率分别为(4.97±0.17)%、(7.82±0.21)%、(11.99±0.21)%、(29.52±0.55)%、(55.23±0.67)%(P<0.05);电镜下PLA作用后NCI-H292细胞呈明显凋亡改变;Western blot检测出细胞中BCL-2/Bax表达降低(P<0.05),活性Caspase 3表达增加(P<0.05)。结论 PLA能引起气道上皮细胞凋亡,并下调BCL-2/Bax表达,上调活性Caspase3表达。Purpose To study the function of poly-L-arginine in inducing the apoptosis of NCI-H292 cells and its influence on the ex- pression of BCL-2/Bax and Caspase 3, then to further reveal the mechanism of airway damage in asthma. Methods NCI-H292 cells were grouped into control group, 10 mg/L PLA group, 20 mg/L PLA group, 40 mg/L PLA group and 60 mg/L PLA group. The apop- tosis rates of NCI-H292 cells of each group after PLA 24-hours-work were detected by flow cytometry, and the morphological changes of apoptosis in NCI-H292 cells among 60 mg/L PLA group were observed by electron microscope. The expression of the Bax, BCL-2 and cleaved Caspase 3 of each group was detected by Western blot. Results The apoptosis rates of NCI-H292 cells in each group respec- tively were (4. 97± O. 17) %, (7. 82 ± O. 21 ) %, ( 11.99 ± 0. 21 ) %, ( 29. 52 ± 0. 55 ) %, ( 55.23 ± 0. 67) %, ( P 〈 O. 05 ). The apoptosis changes of NCI-H292 cells induced by PLA was significant under electron microscope, and the expression of BCL-2/Bax in NCI-H292 cells induced by PLA was statistically decreased ( P 〈 0. 05 ) , and the expression of cleaved Caspase 3 was statistically in- creased ( P 〈 0.05 ). Conclusion PLA can cause the apoptosis of airway epithelial cell by downregulating the expression of BCL-2/ Bax expression and upregulating the expression of cleaved Caspase 3.
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