MicroRNA expression profile of pulmonary artery smooth muscle cells and the effect of let-7d in chronic thromboembolic pulmonary hypertension

被引:28
作者
Wang, Lei [1 ,2 ]
Guo, Li-Juan [1 ,2 ]
Liu, Jie [2 ]
Wang, Wang [2 ]
Yuan, Jason X. -J. [3 ,4 ]
Zhao, Lan [5 ]
Wang, Jun [1 ,2 ]
Wang, Chen [2 ,6 ]
机构
[1] Capital Med Univ, Dept Physiol, Beijing, Peoples R China
[2] Capital Med Univ, Beijing Chao Yang Hosp, Beijing Key Lab Resp & Pulm Circulat Disorders, Beijing, Peoples R China
[3] Univ Illinois, Dept Med, Inst Personalized Resp Med, Chicago, IL USA
[4] Univ Illinois, Dept Pharmacol, Inst Personalized Resp Med, Chicago, IL USA
[5] Imperial Coll London, Div Expt Med, Ctr Pharmacol & Therapeut, London, England
[6] Beijing Hosp, Minist Hlth, Beijing, Peoples R China
基金
中国国家自然科学基金;
关键词
chronic thromboembolic pulmonary hypertension; let-7d; pulmonary artery smooth muscle cell; proliferation;
D O I
10.1086/674310
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Chronic thromboembolic pulmonary hypertension (CTEPH) is a life-threatening condition characterized by single or recurrent pulmonary thromboemboli, which promote pulmonary vascular remodeling. MicroRNA (miRNA), is a small, noncoding RNA that is involved in multiple cell processes and functions and may participate in the pathogenesis of CTEPH. Our aims were to identify the miRNA expression signature in pulmonary artery smooth muscle cells (PASMCs) of CTEPH patients and to study the role of let-7d in CTEPH pathogenesis. The miRNA expression profile was analyzed by microarray in PASMCs of CTEPH and control patients. Differentially expressed miRNAs were selectively validated by stem-loop quantitative real-time reverse-transcription polymerase chain reaction (qRT-PCR). The role of let-7d was identified by in sit/co analysis, and its effect on the proliferation of PASMCs was measured by methyl thiazolyl tetrazolium (MTT). Student's unpaired test, the Fisher exact test, and the x2 test were used for statistical analysis. Eighteen miRNAs were differentially expressed in PASMCs from CTEPH patients, including 12 upregulated miRNAs and 6 downregulated miRNAs; among the latter, let-7d decreased 0.58-fold in CTEPH patients, as validated by qRT-PCR. It was found that let-7d could inhibit the proliferation of PASMCs through upregulation of p21. In conclusion, PASMCs in CTEPH patients have an aberrant miRNA profile and reduced let-7d, which could promote PASMC proliferation and may be involved in the pathogenesis of CTEPH.
引用
收藏
页码:654 / 664
页数:11
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