miR-455-5p Overexpression Reduces Rat Lung Alveolar Type II Cell Proliferation by Downregulating STRA6.

IF 2.1
Anatomical record (Hoboken, N.J. : 2007) Pub Date : 2019-11-01 Epub Date: 2019-06-02 DOI:10.1002/ar.24145
Jintao Zheng, Qiuming He, Huajian Tang, Huimin Xia
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引用次数: 6

Abstract

miR-455-5p and retinoid signaling pathway and its membrane receptor, STRA6, are associated with lung development. Software copredictions indicate that the miRNA upstream of the STRA6 gene is miR-455-5p. We hypothesized that miR-455-5p participates in rat lung alveolar Type II cell proliferation by targeting STRA6 and designed this study to investigate the effects of miR-455-5p overexpression on rat lung alveolar Type II cells. Dual luciferase reporter gene assay was utilized to confirm the relationship between miR-455-5p and STRA6. An miR-455-5p-expressing adenoviral vector was constructed and transfected into rat lung alveolar Type II cells. STRA6 protein expression was detected in rat lung alveolar Type II cells by Western blotting at 72 hr posttransfection. Retinol concentration was detected by ELISA at 72 hr posttransfection. The cell proliferation was detected by CCK8 assay at 24, 48, and 72 hr posttransfection. Our results showed that STRA6 is a target gene of miR-455-5p. STRA6 protein expression was significantly lower in the miR-455-5p-overexpression group than in the NC group (0.615 ± 0.131 vs. 0.958 ± 0.246, P = 0.029). Similar results were observed for retinol concentration (2.985 ± 0.061 vs. 3.949 ± 0.118, P = 0.000). Rat lung alveolar Type II cell proliferation was lower in the miR-455-5p-overexpression group than in the NC group at 24, 48, and 72 hr posttransfection (24 hr: 0.280 ± 0.184 vs. 1.354 ± 0.169 P = 0.026; 48 hr: 0.881 ± 0.016 vs. 1.992 ± 0.050 P = 0.001; 72 hr: 2.105 ± 0.148 vs. 2.937 ± 0.079 P = 0.016). In summary, miR-455-5p is associated with lung development. miR-455-5p overexpression downregulates STRA6, leading to reduced retinol concentration and rat lung alveolar Type II cell proliferation. Anat Rec, 302:2062-2069, 2019. © 2019 The Authors. The Anatomical Record published by Wiley Periodicals, Inc. on behalf of American Association of Anatomists.

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miR-455-5p过表达通过下调STRA6抑制大鼠肺泡II型细胞增殖。
miR-455-5p和类视黄酮信号通路及其膜受体STRA6与肺发育相关。软件预测显示STRA6基因上游的miRNA为miR-455-5p。我们假设miR-455-5p通过靶向STRA6参与大鼠肺泡II型细胞增殖,设计本研究探讨miR-455-5p过表达对大鼠肺泡II型细胞的影响。双荧光素酶报告基因检测证实miR-455-5p与STRA6之间的关系。构建表达mir -455-5p的腺病毒载体,并将其转染大鼠肺泡II型细胞。转染72小时后,用Western blotting检测STRA6蛋白在大鼠肺泡II型细胞中的表达。转染72hr后,ELISA检测视黄醇浓度。转染后24、48、72小时用CCK8法检测细胞增殖情况。我们的研究结果表明,STRA6是miR-455-5p的靶基因。mir -455-5p过表达组STRA6蛋白表达明显低于NC组(0.615±0.131比0.958±0.246,P = 0.029)。视黄醇浓度(2.985±0.061∶3.949±0.118,P = 0.000)与对照组相似。转染后24、48和72小时,mir -455-5p过表达组大鼠肺泡II型细胞增殖低于NC组(24小时:0.280±0.184比1.354±0.169 P = 0.026;48小时:0.881±0.016和1.992±0.050 P = 0.001;72人力资源:2.105±0.148和2.937±0.079 P = 0.016)。综上所述,miR-455-5p与肺发育相关。miR-455-5p过表达下调STRA6,导致视黄醇浓度降低和大鼠肺泡II型细胞增殖。生物医学工程学报,2016,32(2):662 - 669。©2019作者。由Wiley期刊公司代表美国解剖学家协会出版的解剖学记录。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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