MiR‐378a Modulates Macrophage Phagocytosis and Differentiation through Targeting CD47‐SIRPα Axis in Atherosclerosis. (22nd April 2019)

• Record Type: Journal Article
• Authors: Chen, Wenna; Li, Ximing; Wang, Junyan; Song, Nan; Zhu, Aisong; Jia, Lianqun
• Is Part Of: Scandinavian journal of immunology. Volume 90:Number 1(2019)
• Page Start: n/a
• Page End: n/a
• Publication Date: 2019-04-22
• Subjects: atherosclerosis -- inflammation -- micro‐RNA -- SIRPa; Immunology -- Periodicals; 571.96
• DOI: 10.1111/sji.12766
• Languages: English
• ISSNs: 0300-9475

Abstract

Abstract: Background: Signal regulatory protein alpha (SIRPa) is an essential signalling molecule that modulates inflammatory responses in macrophages. However, the regulation of SIRPs and its dynamic changes in macrophages under inflammatory stimulation in atherosclerosis remain uncertain. Objective: The study aimed to identify the miRNAs that regulate SIRPa transcription and their roles in modulating phagocytosis, differentiation and cholesterol efflux in macrophages. Methods: ApoE knockout mice were fed with a high‐fat diet for 12 weeks. Intimal lesion areas and lipid accumulation were assessed by haematoxylin and eosin (HE) and oil red O staining. The expression of mRNAs/miRNAs was assessed by RNA‐seq (RNA sequencing) and RT‐qPCR (real‐time quantitative polymerase chain reaction). The identification of miR‐378a associated with SIRPa regulation in macrophages induced by ox‐LDL was confirmed by RT‐qPCR and Western blot. The phagocytosis and differentiation of macrophages were detected to figure out the role of miR‐378a and SIRPa. Results: SIRPa was proved to be a target of miR‐378a. Reduced miR‐378a can promote the expression of SIRPa. RNA‐seq data showed that the levels of mRNA associated with macrophage phenotypes and SIRPa‐CD47 axis were increasing significantly with a decreasing phagocytic phenotype in ApoE −/− mice vs wild‐type (WT) mice ( P < 0.01). The level of miR‐378a was reduced in the aorta of ApoE −/− mice vs WT mice. The experiment in vitro showed that overexpression of miR‐378a in macrophages decreased the level of Sirpa mRNA obviously vs control ( P < 0.01). The phagocytic activity of miR‐378a–transfected macrophages was promoted vs control ( P < 0.05). miR‐378a significantly depleted Sirpa levels in oxidized low‐density lipoprotein (ox‐LDL)‐stimulated macrophages ( P < 0.05), and depletion of miR‐378a reversed Sirpa reduction obviously ( P < 0.05). miR‐378a promoted the secretion of TNF‐a and IL‐6 indirectly. Conclusion: It has been demonstrated that miR‐378a regulates SIRPa‐mediated phagocytosis and polarization of macrophages by a direct or indirect way. This research may provide a new path to promote reverse cholesterol transport of macrophages and hinder the progress of atherosclerosis.