LIN28B-AS1-IGF2BP1 association is required for LPS-induced NFκB activation and pro-inflammatory responses in human macrophages and monocytes

被引:7
|
作者
Xie, Zichen [1 ]
Zhang, Heng [1 ]
Wang, Jiqin [1 ]
Li, Zhimin [1 ]
Qiu, Chao [1 ]
Sun, Keyu [1 ]
机构
[1] Fudan Univ, Minhang Hosp, Emergency Dept, 39 Xinling Rd, Shanghai 201100, Peoples R China
关键词
LONG NONCODING RNAS; IMMUNOLOGICAL ASPECTS; PROTEINS; STRESS; FAMILY; INJURY;
D O I
10.1016/j.bbrc.2019.09.012
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Insulin-like growth factor 2 (IGF2) mRNA-binding protein 1 (IGF2BP1) mediates lipopolysaccharide (LPS)-induced NF kappa B activation and pro-inflammatory cytokines production in human macrophages. Recent studies have identified a novel IGF2BP1-binding LncRNA LIN28B-AS1. In the present study we show that LPS induced LIN28B-AS1-IGF2BP1 association in THP-1 macrophages, required for LPS-induced IGF2BP1-p65-p52 association and NF kappa B activation. LIN28B-AS1 silencing, by targeted shRNAs, potently inhibited LPS-induced activation of NF kappa B, as well as expression and productions of key pro-inflammatory cytokines, inducing IL-1 beta, IL-6 and TNF-alpha. Conversely, ectopic overexpression of LIN28B-AS1 in THP-1 macrophages potentiated NF kappa B activation and pro-inflammatory cytokines production by LPS. Significantly, LIN28B-AS1 shRNA was ineffective on LPS-induced pro-inflammatory responses in IGF2BP1-knockout THP-1 macrophages. In ex vivo cultured primary human peripheral blood mononuclear cells (PBMCs), LPS-induced IL-1 beta expression and production were attenuated by LIN28B-AS1 shRNA, but augmented with forced LIN28B-AS1 overexpression. Collectively, we show that LIN28B-AS1, binding to IGF2BP1, is required for LPS-induced NF kappa B activation and pro-inflammatory responses in human macrophages. (C) 2019 Elsevier Inc. All rights reserved.
引用
收藏
页码:525 / 532
页数:8
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