Expression profiles and potential roles of transfer RNA-derived small RNAs in atherosclerosis

被引:28
|
作者
He, Xiangqin [1 ]
Yang, Yanyan [2 ]
Wang, Qi [3 ]
Wang, Jueru [4 ]
Li, Shifang [5 ]
Li, Chunrong [5 ]
Zong, Tingyu [1 ]
Li, Xiaolu [1 ]
Zhang, Ying [1 ]
Zou, Yulin [1 ]
Yu, Tao [1 ,6 ]
机构
[1] Qingdao Univ, Affiliated Hosp, Dept Cardiac Ultrasound, 16 Jiangsu Rd, Qingdao 266000, Peoples R China
[2] Qingdao Univ, Basic Med Sch, Dept Immunol, Qingdao, Peoples R China
[3] Xi An Jiao Tong Univ, Affiliated Hosp 1, Dept Cardiol, Xian, Shaanxi, Peoples R China
[4] Qingdao Univ, Affiliated Hosp, Dept Thyroid Surg, Qingdao, Peoples R China
[5] Qingdao Univ, Affiliated Hosp, Dept Neurosurg, Qingdao, Peoples R China
[6] Qingdao Univ, Affiliated Hosp, Inst Translat Med, Qingdao, Peoples R China
基金
中国国家自然科学基金;
关键词
atherosclerosis; cell proliferation; expression profile; non-coding RNAs; tRNA-derived fragments; THERAPEUTIC TARGETS; REGULATES PROLIFERATION; DIAGNOSTIC BIOMARKERS; FRAGMENTS; MECHANISMS; SUPPRESSES; EXOSOMES; REVEALS; CANCER; CELL;
D O I
10.1111/jcmm.16719
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Knowledge regarding the relationship between the molecular mechanisms underlying atherosclerosis (AS) and transfer RNA-derived small RNAs (tsRNAs) is limited. This study illustrated the expression profile of tsRNAs, thus exploring its roles in AS pathogenesis. Small RNA sequencing was performed with four atherosclerotic arterial and four healthy subject samples. Using bioinformatics, the protein-protein interaction network and cellular experiments were constructed to predict the enriched signalling pathways and regulatory roles of tsRNAs in AS. Of the total 315 tsRNAs identified to be dysregulated in the AS group, 131 and 184 were up-regulated and down-regulated, respectively. Interestingly, the pathway of the differentiated expression of tsRNAs in cell adhesion molecules (CAMs) was implicated to be closely associated with AS. Particularly, tRF-Gly-GCC might participate in AS pathogenesis via regulating cell adhesion, proliferation, migration and phenotypic transformation in HUVECs and VSMCs. In conclusion, tsRNAs might help understand the molecular mechanisms of AS better. tRF-Gly-GCC may be a promising target for suppressing abnormal vessels functions, suggesting a novel strategy for preventing the progression of atherosclerosis.
引用
收藏
页码:7052 / 7065
页数:14
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