Qin Song, Chen Miao, Ji Hui, Liu Guoyue, Chen Tao, Li Kang, Mei Hong
Department of Critical Care Medicine, the First Affiliated Hospital of Zunyi Medical College, Zunyi 563003, Guizhou, China. Corresponding author: Chen Miao, Email:
Zhonghua Wei Zhong Bing Ji Jiu Yi Xue. 2015 Jul;27(7):574-8. doi: 10.3760/cma.j.issn.2095-4352.2015.07.007.
To study the effect of hydrogen peroxide (H2O2) in inducing apoptosis of type II alveolar epithelial cell (AECII) after overexpression by adenoviral transfection of micro RNA-21-5p (miR-21-5p), and to explore the mechanism of its anti-apoptosis.
Subculture AECII were randomly divided into four groups: normal control group (normal saline), H2O2 challenge group (0.5 mmol/L H2O2), miR-21-5p overexpression group (miR-21-5p adenovirus+0.5 mmol/L H2O2), miR-21-5p negative transfection group (adenovirus void+0.5 mmol/L H2O2). Transmission electron microscopy and flow cytometry were used to detect apoptotic morphology and early apoptotic rate. Real-time fluorescence quantitative reverse transcription-polymerase chain reaction (RT-PCR) was used to detect the expression of miR-21-5p in AECII, and Western Blot was used to detect the protein expressions of Bcl-2, Bax, and caspase-3 at the highest transfection efficiency at different time points (6, 12, 24, 48 hours).
(1) AECII identification: fluorescence microscopy showed the presence of characteristic structure of AECII, i.e. microvilli and osmiophilic lamellar bodies. (2) Apoptotic morphology: transmission electron microscopy showed cytoplasmic retraction, chromatin condensation, margination, lack of cell surface microvilli, and emptying of osmiophilic lamellar bodies in AECII. (3) The expression of miR-21-5p in AECII: the highest transfection efficiency was found at 48 hours. The expression of miR-21-5p in miR-21-5p overexpression group was significantly higher than that of the normal control group, H2O2 challenge group and miR-21-5p negative transfection group (A value: 1.54±0.02 vs. 1.02±0.02, 0.56±0.03, 0.58±0.02, all P<0.05). (4) The rate of early apoptosis: compared with normal control group, the early apoptotic rates in H2O2 challenge group, miR-21-5p negative transfection group and miR-21-5p overexpression group were gradually elevated with the prolongation of injury time. The early apoptotic rate in miR-21-5p overexpression group was significantly lower than that of the H2O2 challenge group and miR-21-5p negative transfection group at all time points except 6 hours [12 hours: (10.73±2.80)% vs. (16.26±0.59)%, (16.04±0.70)%; 24 hours: (16.00±3.44)% vs. (23.29±2.78)%, (23.58±2.31)%; 48 hours: (31.30±3.55)% vs. (50.53±2.17)%, (49.41±1.97)%, all P<0.05]. There was no significant difference in early apoptotic rate between miR-21-5p negative transfection group and H2O2 challenge group at each time point. (5) Protein expression: the expressions of Bax and caspase-3 in miR-21-5p overexpression group were significantly lower than those of the H2O2 challenge group and miR-21-5p negative transfection group [Bax (A value): 0.07±0.01 vs. 0.18±0.01, 0.13±0.01; caspase-3 (A value): 0.07±0.01 vs. 0.23±0.01, 0.12±0.01, all P<0.05], and Bcl-2 protein expression was significantly higher than that of the H2O2 challenge group and miR-21-5p negative transfection group (A value: 0.26±0.01 vs. 0.06±0.01, 0.10±0.01, both P<0.05).
(1) miR-21-5p has the function of anti-apoptosis of AECII. (2) Adenoviral vector is a successful gene transfer vector when transfected with AECII. (3) The anti-apoptosis of AECII by miR-21-5p may be associated with reduced Bax and caspase-3 protein levels and raised expression levels of Bcl-2 protein.
研究经腺病毒转染微小RNA-21-5p(miR-21-5p)过表达后过氧化氢(H₂O₂)对Ⅱ型肺泡上皮细胞(AECII)凋亡的影响,并探讨其抗凋亡机制。
将传代培养的AECII随机分为四组:正常对照组(生理盐水)、H₂O₂刺激组(0.5 mmol/L H₂O₂)、miR-21-5p过表达组(miR-21-5p腺病毒+0.5 mmol/L H₂O₂)、miR-21-5p阴性转染组(空腺病毒+0.5 mmol/L H₂O₂)。采用透射电子显微镜和流式细胞术检测凋亡形态和早期凋亡率。采用实时荧光定量逆转录-聚合酶链反应(RT-PCR)检测AECII中miR-21-5p的表达,采用蛋白质免疫印迹法检测不同时间点(6、12、24、48小时)转染效率最高时Bcl-2、Bax和caspase-3的蛋白表达。
(1)AECII鉴定:荧光显微镜显示存在AECII的特征性结构,即微绒毛和嗜锇板层小体。(2)凋亡形态:透射电子显微镜显示AECII出现细胞质收缩、染色质凝聚、边缘化、细胞表面微绒毛缺失和嗜锇板层小体排空。(3)AECII中miR-21-5p的表达:48小时转染效率最高。miR-21-5p过表达组中miR-21-5p的表达明显高于正常对照组、H₂O₂刺激组和miR-21-5p阴性转染组(A值:1.54±0.02 vs. 1.02±0.02、0.56±0.03、0.58±0.02,均P<0.05)。(4)早期凋亡率:与正常对照组相比,H₂O₂刺激组、miR-21-5p阴性转染组和miR-21-5p过表达组的早期凋亡率随损伤时间延长逐渐升高。除6小时外,miR-21-5p过表达组在各时间点的早期凋亡率均明显低于H₂O₂刺激组和miR-21-5p阴性转染组[12小时:(10.73±2.80)% vs.(16.26±0.59)%、(16.04±0.70)%;24小时:(16.00±3.44)% vs.(23.29±2.78)%、(23.58±2.31)%;48小时:(31.30±3.55)% vs.(50.53±2.17)%、(49.41±1.97)%,均P<0.05]。miR-21-5p阴性转染组与H₂O₂刺激组在各时间点的早期凋亡率无明显差异。(5)蛋白表达:miR-21-5p过表达组中Bax和caspase-3的表达明显低于H₂O₂刺激组和miR-21-5p阴性转染组[Bax(A值):0.07±0.01 vs. 0.18±0.01、0.13±0.01;caspase-3(A值):0.07±0.01 vs. 0.23±0.01、0.12±0.01,均P<0.05],Bcl-2蛋白表达明显高于H₂O₂刺激组和miR-21-5p阴性转染组(A值:0.26±0.01 vs. 0.06±0.01、0.10±0.01,均P<0.05)。
(1)miR-21-5p具有抗AECII凋亡的作用。(2)腺病毒载体转染AECII时是一种成功的基因转移载体。(3)miR-21-5p对AECII的抗凋亡作用可能与降低Bax和caspase-3蛋白水平以及提高Bcl-2蛋白表达水平有关。