| Literature DB >> 28965281 |
Pengfei Zhang1, Hong Wang1, Xueting Luo2, Haiyun Liu1, Bing Lu1, Tong Li1, Shiqi Yang1, Qing Gu2, Bin Li3,4, Fenghua Wang5,6, Xiaodong Sun7,8,9.
Abstract
Arg-1+Ym-1+ M2-type macrophages play essential roles in the development of choroidal neovascularization (CNV). Thus, inhibition of M2-type macrophages may be effective in suppressing CNV. However, the potential mechanisms of macrophage polarization during development of CNV remain unclear. In this study, we report that microRNA-155 (miR-155) inhibited M2 polarization by targeting C/EBPβ in CNV model mice and in bone marrow-derived primary macrophages. Moreover, our data show that intravitreous injection of miR-155 mimics suppressed subretinal leakage and neovascularization. Therefore, we conclude that C/EBPβ plays a significant role in M2 macrophage polarization in CNV model, while miR-155 mimics could suppress CNV by inhibiting C/EBPβ activity and M2 macrophage polarization.Entities:
Keywords: C/EBPβ; choroidal neovascularization; macrophages; miRNA-155; polarization
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Year: 2018 PMID: 28965281 DOI: 10.1007/s10753-017-0672-8
Source DB: PubMed Journal: Inflammation ISSN: 0360-3997 Impact factor: 4.092