Tropoelastin基因单核苷酸多态性突变影响人主动脉平滑肌细胞Tropoelastin mRNA和弹力蛋白的表达。

DNA and cell biology Pub Date : 2023-12-01 Epub Date: 2023-11-21 DOI:10.1089/dna.2023.0108
Jie Yue, You-Fei Qi, Wen-Bo Zhang, Sa-Hua Liu, Hao Chen, Zhen-Zhen Li, Hong-Fei Wu
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Afterward, HASMCs were infected with recombinant lentiviruses, and the positive cells sorted by flow cytometry were amplified. Four stable HASMCs cell lines including pWSLV-02-ELN, pWSLV-02-ELN-mut1, pWSLV-02-ELN-mut2, and pWSLV-02 vector were constructed. The expressions of tropoelastin mRNA and elastin in HASMCs were detected by real-time quantitative reverse transcription-PCR and western blot, respectively. Recombinant plasmids including pWSLV-02-ELN-mut1, pWSLV-02-ELN-mut2, and pWSLV-02-ELN were successfully constructed. Recombinant lentiviruses carrying tropoelastin gene were obtained via lentivirus packaging. After infection for 24 h, 3 days and 5 days in HASMCs, tropoelastin mRNA expressions in pWSLV-02-ELN-mut1 and pWSLV-02-ELN-mut2 groups were significantly lower than that of pWSLV-02-ELN group. Besides, after infection for 24 h, 3 days, and 5 days, elastin levels in pWSLV-02-ELN-mut1 and pWSLV-02-ELN-mut2 groups were significantly lower than that in pWSLV-02-ELN group. 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引用次数: 0

摘要

本研究旨在探讨肌弹性蛋白基因单核苷酸多态性(snp)对人主动脉平滑肌细胞(HASMCs)肌弹性蛋白mRNA和弹性蛋白表达的影响。选择rs2071307 (G/A)和rs1785598 (G/C)两个SNP位点,构建携带野生型和突变型tropoelastin基因的重组慢病毒载体。构建重组质粒pWSLV-02-ELN、pWSLV-02-ELN-mut1、pWSLV-02-ELN-mut2,经PCR扩增并测序。将制备的质粒与包装质粒pVSV-G和psPAX2共转染HEK293T细胞,获得携带tropoelastin基因的重组慢病毒。然后用重组慢病毒感染HASMCs,流式细胞术扩增阳性细胞。构建了4株稳定的HASMCs细胞株pWSLV-02- eln、pWSLV-02- eln -mut1、pWSLV-02- eln -mut2和pWSLV-02载体。采用实时定量逆转录- pcr和western blot分别检测HASMCs中tropoelastin mRNA和elastin的表达。成功构建了重组质粒pWSLV-02-ELN-mut1、pWSLV-02-ELN-mut2和pWSLV-02-ELN。通过慢病毒包装获得了携带弹力蛋白基因的重组慢病毒。感染24 h、3 d和5 d后,pWSLV-02-ELN-mut1和pWSLV-02-ELN-mut2组的tropoelastin mRNA表达量均显著低于pWSLV-02-ELN组。感染24 h、3 d、5 d后,pWSLV-02-ELN-mut1组和pWSLV-02-ELN-mut2组的弹性蛋白水平均显著低于pWSLV-02-ELN组。综上所述,肌弹性蛋白基因snp突变影响了肌弹性蛋白mRNA和弹性蛋白的表达,提示肌弹性蛋白基因rs2071307和rs17855988的多态性可能是AD发生的重要因素。
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Single Nucleotide Polymorphisms Mutation of Tropoelastin Gene Affects Tropoelastin mRNA and Elastin Expressions in Human Aortic Smooth Muscle Cells.

We aimed to explore the effects of single nucleotide polymorphisms (SNPs) in tropoelastin gene on tropoelastin mRNA and elastin expressions in human aortic smooth muscle cells (HASMCs). Two SNP loci, rs2071307 (G/A) and rs1785598 (G/C), were selected to construct recombinant lentivirus vectors carrying wild-type and mutant tropoelastin gene. Recombinant plasmids including pWSLV-02-ELN, pWSLV-02-ELN-mut1, and pWSLV-02-ELN-mut2 were constructed, before being amplified by polymerase chain reaction (PCR) and sequenced. The prepared plasmids and the packaging plasmids (pVSV-G and psPAX2) were cotransfected into HEK293T cells to obtain recombinant lentiviruses carrying tropoelastin gene. Afterward, HASMCs were infected with recombinant lentiviruses, and the positive cells sorted by flow cytometry were amplified. Four stable HASMCs cell lines including pWSLV-02-ELN, pWSLV-02-ELN-mut1, pWSLV-02-ELN-mut2, and pWSLV-02 vector were constructed. The expressions of tropoelastin mRNA and elastin in HASMCs were detected by real-time quantitative reverse transcription-PCR and western blot, respectively. Recombinant plasmids including pWSLV-02-ELN-mut1, pWSLV-02-ELN-mut2, and pWSLV-02-ELN were successfully constructed. Recombinant lentiviruses carrying tropoelastin gene were obtained via lentivirus packaging. After infection for 24 h, 3 days and 5 days in HASMCs, tropoelastin mRNA expressions in pWSLV-02-ELN-mut1 and pWSLV-02-ELN-mut2 groups were significantly lower than that of pWSLV-02-ELN group. Besides, after infection for 24 h, 3 days, and 5 days, elastin levels in pWSLV-02-ELN-mut1 and pWSLV-02-ELN-mut2 groups were significantly lower than that in pWSLV-02-ELN group. In conclusion, SNPs mutation of tropoelastin gene affected the expression of tropoelastin mRNA and elastin, suggesting that the polymorphisms of rs2071307 and rs17855988 in tropoelastin gene might be important factors for AD development.

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