4.7 Article

Research paper Hsa_circ_0007478 aggravates NLRP3 inflammasome activation and lipid metabolism imbalance in ox-LDL-stimulated macrophage via miR-765/ EFNA3 axis

期刊

CHEMICO-BIOLOGICAL INTERACTIONS
卷 368, 期 -, 页码 -

出版社

ELSEVIER IRELAND LTD
DOI: 10.1016/j.cbi.2022.110195

关键词

Hsa_circ_0007478; MiR-765; Atherosclerosis; NLRP3 inflammasome; Lipid metabolism

资金

  1. Zhejiang Provincial Natural Science Foundation of China [LY22H020004, LQ21H020009]
  2. National Natural Science Foundation of China [82070446, 82003750]
  3. Wenzhou Science and Technology Bureau [Y20210136]
  4. Key Research and Development Program of Zhejiang Province [2019C03012]
  5. Research Funds project of Wenzhou Medical University [KYYW202017]

向作者/读者索取更多资源

This study found that circular RNA hsa_circ_0007478 was upregulated in ox-LDL-stimulated macrophages, accompanied by reduced miR-765 and increased EFNA3 expression. Silencing of hsa_circ_0007478 or transfection of miR-765 mimics decreased the activation of NLRP3 inflammasome and IL-113 in macrophages. Hsa_circ_0007478 promoted EFNA3 expression by acting as a miR-765 sponge. These findings suggest that hsa_circ_0007478 may play an important role in the inflammatory response and foam cell formation in atherosclerosis.
Coronary heart disease can be effectively prevented by alleviating atherosclerotic plaque progression. Ox-LDL-induced inflammatory response in macrophages is a critical factor in the pathophysiology of atherosclerosis. It is well known that circular RNAs (circRNAs) are associated with the progression of several human diseases, such as coronary artery diseases, by sponging microRNAs (miRNAs), but the function and hidden mechanisms of circRNAs in macrophage inflammation and lipid metabolism remain unclear. In our study, we established an ox-LDL-stimulated macrophage model and used microarray to detect circRNA expression in macrophages. The re-sults revealed distinct profiles of circRNA expression across the ox-LDL-stimulated macrophage group and the control group. Among them, hsa_circ_0007478 was upregulated in ox-LDL-stimulated macrophages, accompa-nied by reduced miR-765 and increased EFNA3 expression. Activation of NLRP3 inflammasome and IL-113 in macrophages was decreased following silencing of hsa_circ_0007478 or transfection of miR-765 mimics. In addition, we demonstrated that as a direct target gene of miR-765, the expression of EFNA3 regulated NLRP3 inflammasome and IL-113 levels in macrophages. Besides, hsa_circ_0007478 promoted EFNA3 expression by acting as a miR-765 sponge. We further showed that hsa_circ_0007478/miR-765/EFNA3 axis could also be involved in the inhibition of the lipid metabolism and foam cells formation in ox-LDL-macrophages. Taken together, these findings suggest that Hsa_circ_0007478 may be a potential molecular target against the inflam-matory response and foam cells during atherosclerosis.

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