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重组人 KAI1/CD82 通过阻断 TLR4/JNK/NF-κB 信号通路抑制 LPS 诱导的 RAW264.7 细胞 M1 型极化。

Recombinant human KAI1/CD82 attenuates M1 macrophage polarization on LPS-stimulated RAW264.7 cells via blocking TLR4/JNK/NF-κB signal pathway.

机构信息

Department of Convergence Medicine, Pusan National University School of Medicine, Yangsan 50612, Korea.

Department of Convergence Medicine, Pusan National University School of Medicine, Yangsan 50612; PNU GRAND Convergence Medical Science Education Research Center, Pusan National University School of Medicine, Yangsan 50612, Korea.

出版信息

BMB Rep. 2023 Jun;56(6):359-364. doi: 10.5483/BMBRep.2022-0189.

Abstract

KAI1/CD82, a membrane tetraspanin protein, can prevent various cancers and retinal disorders through its anti-angiogenic and anti-metastatic capacity. However, little is known about its anti-inflammatory effect and molecular mechanism. Therefore, the present study aimed to inLPSvestigate effect of a recombinant protein of the large extracellular domain of human KAI1 (Gly 111-Leu 228, rhKAI1) on lipopolysaccharides (LPS)-stimulated RAW264.7 macrophage-like cells and mouse bone marrow-derived macrophages (BMDM) and to identify its underlying mechanism. Our data showed that rhKAI1 suppressed expression levels of classically macrophages (M1) phenotyperelated surface markers F4/80+CD86+ in LPS-stimulated BMDM and RAW264.7 cells. In addition, LPS markedly increased mRNA expression and release levels of pro-inflammatory cytokines and mediators such as interleukin (IL)-1β, IL-6, tumor necrosis factor-α, cyclooxygenase-2, nitric oxide and prostaglandin E2, whereas these increases were substantially down-regulated by rhKAI1. Furthermore, LPS strongly increased expression of NF-κB p65 in the nuclei and phosphorylation of ERK, JNK, and p38 MAPK. However, nuclear translocation of NF-κB p65 and phosphorylation of JNK were greatly reversed in the presence of rhKAI1. Especially, rhKAI1 markedly suppressed expression of toll-like receptor (TLR4) and prevented binding of LPS with TLR4 through molecular docking predict analysis. Importantly, Glu 214 of rhKAI1 residue strongly interacted with Lys 360 of TLR4 residue, with a binding distance of 2.9 Å. Taken together, these findings suggest that rhKAI1 has an anti-inflammatory effect on LPS-polarized macrophages by interacting with TLR4 and down-regulating the JNK/NF-κB signaling pathway. [BMB Reports 2023; 56(6): 359-364].

摘要

KAI1/CD82 是一种膜四跨膜蛋白,通过其抗血管生成和抗转移能力可以预防多种癌症和视网膜疾病。然而,其抗炎作用及其分子机制知之甚少。因此,本研究旨在探讨人 KAI1 大细胞外域重组蛋白(Gly 111-Leu 228,rhKAI1)对脂多糖(LPS)刺激的 RAW264.7 样巨噬细胞和小鼠骨髓来源巨噬细胞(BMDM)的作用,并鉴定其潜在机制。我们的数据表明,rhKAI1 抑制 LPS 刺激的 BMDM 和 RAW264.7 细胞中经典巨噬细胞(M1)表型相关表面标志物 F4/80+CD86+的表达水平。此外,LPS 显著增加促炎细胞因子和介质(如白细胞介素(IL)-1β、IL-6、肿瘤坏死因子-α、环氧化酶-2、一氧化氮和前列腺素 E2)的 mRNA 表达和释放水平,而 rhKAI1 则显著下调这些水平。此外,LPS 强烈增加核内 NF-κB p65 的表达和 ERK、JNK 和 p38 MAPK 的磷酸化。然而,在存在 rhKAI1 的情况下,NF-κB p65 的核易位和 JNK 的磷酸化得到了很大逆转。特别是,rhKAI1 显著抑制 TLR4 的表达,并通过分子对接预测分析防止 LPS 与 TLR4 结合。重要的是,rhKAI1 残基上的 Glu214 与 TLR4 残基上的 Lys360 强烈相互作用,结合距离为 2.9 Å。总之,这些发现表明 rhKAI1 通过与 TLR4 相互作用并下调 JNK/NF-κB 信号通路对 LPS 极化的巨噬细胞具有抗炎作用。[BMB 报告 2023;56(6): 359-364]。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/399e/10315567/6701b3aceb72/bmb-56-6-359-f1.jpg

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