Xu Ran, Zhu Dan, Guo Jianghong, Wang Chong
Department of Cardiovascular Surgery, Shanghai Chest Hospital, Shanghai Jiao Tong University, Shanghai, China.
Department of Cardiovascular Surgery, Shanghai Chest Hospital, Shanghai Jiao Tong University, Shanghai, China.
Can J Cardiol. 2021 Sep;37(9):1460-1471. doi: 10.1016/j.cjca.2021.04.007. Epub 2021 May 10.
Calcific aortic-valve disease (CAVD) is the most common cause of aortic valve replacement in developed countries. Intraleaflet hemorrhage has been found to be positively correlated with the progression of CAVD. Although most research has focused on erythrocyte degradation products, which promote progression of CAVD, the process of erythrophagocytosis and erythrocyte degradation by macrophages in intraleaflet hemorrhage areas has remained unexplored.
The erythrocyte degradation products of aortic valve specimens were detected by Perls' staining and quantified. The gene and protein expression levels of interleukin (IL)-18 in THP-1-polarized macrophages cultured in osteogenic medium were tested. We also quantified the iron and heme degraded by macrophages and analyzed the expression of ferroportin (FPN) and heme oxygenase-1 (HO-1) in the osteogenic medium. Furthermore, we tested the mRNA and protein levels of osteoblast markers in valve interstitial cells after co-culture with M1 macrophages treated with IL-18 and erythrocytes.
Our experiments demonstrated that IL-18 activates HO-1 and FPN to promote erythrophagocytosis and erythrocyte degradation by macrophages in a calcific microenvironment via p38 and Erk1/2. We also found that the calcific microenvironment promotes IL-18 mRNA and protein expression in THP-1-polarized macrophages.
In conclusion, IL-18 promotes M1 macrophage-mediated erythrophagocytosis and erythrocyte degradation by regulating the activation of HO-1 and FPN via p38 and Erk1/2 in a calcific microenvironment.
钙化性主动脉瓣疾病(CAVD)是发达国家主动脉瓣置换最常见的原因。已发现瓣叶内出血与CAVD的进展呈正相关。尽管大多数研究集中在促进CAVD进展的红细胞降解产物上,但瓣叶内出血区域巨噬细胞的红细胞吞噬和红细胞降解过程仍未得到探索。
采用普鲁士蓝染色检测并定量主动脉瓣标本的红细胞降解产物。检测在成骨培养基中培养的THP-1极化巨噬细胞中白细胞介素(IL)-18的基因和蛋白表达水平。我们还定量了巨噬细胞降解的铁和血红素,并分析了成骨培养基中铁转运蛋白(FPN)和血红素加氧酶-1(HO-1)的表达。此外,我们检测了与经IL-18和红细胞处理的M1巨噬细胞共培养后瓣膜间质细胞中成骨细胞标志物的mRNA和蛋白水平。
我们的实验表明,IL-18通过p38和Erk1/2激活HO-1和FPN,以促进钙化微环境中巨噬细胞的红细胞吞噬和红细胞降解。我们还发现钙化微环境促进THP-1极化巨噬细胞中IL-18 mRNA和蛋白的表达。
总之,IL-18通过在钙化微环境中经由p38和Erk1/2调节HO-1和FPN的激活,促进M1巨噬细胞介导的红细胞吞噬和红细胞降解。