腹主动脉瘤
巨噬细胞
上睑下垂
磷酰胆碱
动脉瘤
化学
基因剔除小鼠
细胞生物学
免疫学
癌症研究
医学
生物
炎症
生物化学
体外
外科
受体
炎症体
作者
Xu Zhang,Fangda Li,Wei Wang,Lei Ji,Bo Sun,Xue Xiao,Xiaoxiao Wang,Yuexin Chen,Bao Liu,Wei Ye,Cui Tian,Hongxia Wang,Yuehong Zheng
标识
DOI:10.1016/j.bbrc.2020.09.082
摘要
Macrophages contribute to abdominal aortic aneurysm (AAA), but the effect of macrophage on AAA formation is not totally understood. Recent research proved that macrophage pyroptosis plays an important role in many cardiovascular disease. However, whether macrophage pyroptosis is involved in AAA and its mechanism remains unknown. In this study, we found that the pyroptosis significantly increased in AAA tissues. β5i inhibitor PR-957 treatment or β5i deficiency markedly ameliorated AAA formation and decreased the pyroptosis. Pyroptosis were also significantly attenuated in bone marrow derived macrophages (BMDM) from β5i−/- mice compared with the control group when they were subjected to OXLDL. Mechanistically, β5i may promote activation of NFκB which augment NLRP3 expression. In conclusion, this study suggested macrophages pyroptosis are involved in AAA and inhibition or knockout of β5i decreased macrophage pyroptosis via IκB/NFκB pathway.
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