A protective polymorphism in MMP16, improved blood gas levels, and chronic obstructive pulmonary diseases: Family and two population‐based studies. Issue 7 (14th April 2020)

• Record Type: Journal Article
• Authors: Zhang, Zili; Wang, Jian; Zheng, Zeguang; Chen, Xindong; Xu, Guihua; Chen, Sifan; Liu, Fei; Chen, Lingdan; Ding, Mingjing; Yuan, Liang; Li, Yuanyuan; Qian, Jing; Xie, Xiaohui; Deng, Bingxian; Lu, Wenju
• Is Part Of: Human mutation. Volume 41:Issue 7(2020)
• Page Start: 1280
• Page End: 1297
• Publication Date: 2020-04-14
• Subjects: blood gas -- COPD -- Hsa‐miR‐576‐5p -- MMP16 -- WGS; Human chromosome abnormalities -- Periodicals; Mutation (Biology) -- Periodicals; 616.04205
• DOI: 10.1002/humu.24013
• Languages: English
• ISSNs: 1059-7794

Abstract

Abstract: The aberrant expression of matrix metalloproteinases ( MMPs ) is known to contribute to the pathogenesis of airway remodeling and alveolar disruption in chronic obstructive pulmonary disease (COPD). In the discovery stage, 11 COPD from five families were subjected to whole‐genome sequencing, and 21 common polymorphisms in MMPs and TIMPs were identified. These polymorphisms were genotyped in two subsequent verification studies. Of these polymorphisms, c.2392G>A (rs2664370T>C) and c.4158C>A (rs2664369T>G) in MMP16 remained significantly different. Functionally, we found that MMP16 expression was significantly increased in peripheral blood monocytes (PBMCs) from COPD and in cigarette smoke extract‐treated 16HBE cells compared with controls. This was also shown by bioinformatics analysis. COPD carrying rs2664370CC showed decreased levels of MMP16 in the plasma and in PBMCs compared with those carrying CT and TT. Treatment with hsa‐miR‐576‐5p mimics led to a greater reduction in luciferase reporter activity in cells transfected with rs2664370CC. Moreover, blood levels of base excess, PCO2, and PO2 in COPD with rs2664370CC were significantly lower than those with rs2664370CT+TT. Taken together, these results demonstrate that the rs2664370T>C polymorphism in MMP16 protects against the risk of COPD, likely by favoring interaction with hsa‐miR‐576‐5p, leading to reduced MMP16 expression and improved blood gas levels.