Role of long non-coding RNA TCONS_02443383 in regulating cell adhesion and peroxisome proliferator-activated receptor (PPAR) signaling genes in atherosclerosis: A New Zealand white rabbit model study

被引:0
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作者
Yilihamu, Yilinuer [1 ]
Xu, Rui [1 ]
Jia, Wenxiao [1 ]
Kukun, Hanjiaerbieke [1 ]
Aihemaiti, Dilinuerkezi [1 ]
Chang, Yifan [1 ]
Ding, Shuang [1 ]
Wang, Yunling [1 ]
机构
[1] Xinjiang Med Univ, Affiliated Hosp 1, Dept Radiol, 137 South Liyushan Rd, Urumqi 830054, Xinjiang, Peoples R China
关键词
Aortic atherosclerosis; High-throughput sequencing; New Zealand white rabbit; PROMOTES; ANNOTATION; MECHANISMS; MUSCLE;
D O I
10.1016/j.gene.2024.148694
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Objective: In this study, we performed RNA sequencing (RNA-seq) on the abdominal aorta tissue of New Zealand rabbits and investigated the potential association of lncRNA TCONS_02443383 with the development of AS through bioinformatics analysis of the sequencing data. The obtained results were further validated using quantitative real-time polymerase chain reaction (qRT-PCR). Method: We induced an AS model in New Zealand rabbits by causing balloon injury to the abdominal aorta vascular wall and administering a high-fat diet. We then upregulated the expression level of the lncRNA TCONS_02443383 by injecting lentiviral plasmids through the ear vein. RNA sequencing (RNA-seq) was performed on the abdominal aorta tissues. We conducted Kyoto Encyclopedia of Genes and Genomes (KEGG) signaling pathway and Gene Ontology (GO) analyses. Result: The overexpression of the lncRNA TCONS_02443383 led to an upregulation of peroxisome proliferatoractivated receptor (PPAR) signaling pathways as well as genes related to cell adhesion. Conclusion: The overexpression of the lncRNA TCONS_02443383 can inhibit the occurrence and development of AS by upregulating peroxisome proliferator-activated receptor (PPAR) signaling pathways and genes related to cell adhesion.
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页数:12
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