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间充质干细胞条件培养基的抗炎作用抑制了体外巨噬细胞的激活。

Anti-inflammatory effects of mesenchymal stem cell-conditioned media inhibited macrophages activation in vitro.

机构信息

Department of Orthopaedic Surgery, Chonnam National University Medical School and Hospital, 322 Seoyang-ro, Hwasun-eup, Hwasun-gun, Jeollanam-do, Republic of Korea.

Department of Orthopaedic Surgery, Affiliated Sir Run Run Hospital of Nanjing Medical University, Nanjing, Jiangsu, People's Republic of China.

出版信息

Sci Rep. 2022 Mar 19;12(1):4754. doi: 10.1038/s41598-022-08398-4.

Abstract

The immunomodulatory effects of mesenchymal stem cells (MSCs) on macrophages have been reported, however, the underlying mechanism remains unknown. Therefore, this study aimed to investigate the anti-inflammatory effects of MSCs on lipopolysaccharide (LPS)-stimulated macrophages and the subsequent downregulation of their inflammatory mediators. Macrophages were treated with conditioned media from MSCs, without a subsequent change of MSCs responding to the inflammation state. This study also evaluated whether the interleukin (IL) 4 stimulation of MSCs can improve their anti-inflammatory effects. Results demonstrated that the MSC-conditioned medium (MSC-CM) stimulated with IL4 significantly inhibited inducible nitric oxide synthase (iNOS) and cyclooxygenase-2 (COX-2) protein expression of LPS-activated macrophages. MSC-CM treatment inhibited the mRNA transcription of the cytokines IL1β and IL6, the chemokines C-C motif ligand (CCL) 2, CCL3, CCL4, and CCL5, and the chemokine receptors CCR2 and CCR5, in LPS-stimulated macrophages. As revealed through western blot and immunofluorescence analyses, the phosphorylation of p38, JNK, and ERK MAPKs, as well as phosphorylation of NF-κB in stimulated macrophages, were also inhibited by the MSC-CM. Further, more potent anti-inflammatory effects were observed with the IL4-stimulated cells, compared with those observed with the non-stimulated cells. The MSC-CM demonstrated a potent anti-inflammatory effect on LPS-activated macrophages, while the IL4 stimulation improved this effect. These findings indicate that MSCs could exert anti-inflammatory effects on macrophages, and may be considered as a therapeutic agent in inflammation treatment.

摘要

间充质干细胞 (MSCs) 对巨噬细胞的免疫调节作用已有报道,但具体机制尚不清楚。因此,本研究旨在探讨 MSCs 对脂多糖 (LPS) 刺激的巨噬细胞的抗炎作用及其对炎症介质的下调作用。巨噬细胞用 MSC 的条件培养基(MSC-CM)处理,而不改变 MSC 对炎症状态的反应。本研究还评估了 IL4 刺激 MSCs 是否可以改善其抗炎作用。结果表明,IL4 刺激的 MSC 条件培养基 (MSC-CM) 显著抑制 LPS 激活的巨噬细胞中诱导型一氧化氮合酶 (iNOS) 和环氧化酶-2 (COX-2) 蛋白的表达。MSC-CM 处理抑制了 LPS 刺激的巨噬细胞中细胞因子 IL1β 和 IL6、趋化因子 C-C 基序配体 (CCL) 2、CCL3、CCL4 和 CCL5 以及趋化因子受体 CCR2 和 CCR5 的 mRNA 转录。通过 Western blot 和免疫荧光分析显示,MSC-CM 还抑制了刺激巨噬细胞中 p38、JNK 和 ERK MAPKs 的磷酸化以及 NF-κB 的磷酸化。进一步的研究发现,与未刺激的细胞相比,IL4 刺激的细胞具有更强的抗炎作用。MSC-CM 对 LPS 激活的巨噬细胞具有强大的抗炎作用,而 IL4 刺激则增强了这种作用。这些发现表明,MSCs 可以对巨噬细胞发挥抗炎作用,并且可以被认为是炎症治疗的一种治疗剂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51e4/8934344/be6d42c0000b/41598_2022_8398_Fig1_HTML.jpg

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