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微小 RNA21 可在巨噬细胞中引发炎症反应,外泌体可作为其传递载体。

MicroRNA 21 Elicits a Pro-inflammatory Response in Macrophages, with Exosomes Functioning as Delivery Vehicles.

机构信息

Department of Applied Physiology, Faculty of Medicine, University of Miyazaki, Kihara 5200, Kiyotake Cho, Miyazaki, 889-1692, Japan.

出版信息

Inflammation. 2021 Aug;44(4):1274-1287. doi: 10.1007/s10753-021-01415-0. Epub 2021 Jan 26.

DOI:10.1007/s10753-021-01415-0
PMID:33501624
Abstract

MicroRNAs can regulate inflammatory responses by modulating macrophage polarization. Although microRNA miR-21 is linked to crucial processes involved in inflammatory responses, its precise role in macrophage polarization is controversial. In this study, we investigated the functional relevance of endogenous miRNA-21 and the role of exosomes. RAW 264.7 macrophages were transfected with miR-21 plasmid, and the inflammatory response was evaluated by flow cytometry, phagocytosis, and real-time PCR analysis of inflammatory cytokines. To understand the signaling pathways' role, the cells were treated with inhibitors specific for PI3K or NFĸB. Exosomes from transfected cells were used to study the paracrine action of miR-21 on naive macrophages. Overexpression of miR-21 resulted in significant upregulation of pro-inflammatory cytokines, pushing the cells towards a pro-inflammatory phenotype, with partial involvement of PI3K and NFĸB signal pathways. The cells also secreted miR-21 rich exosomes, which, on delivery to naive macrophages, caused them to exhibit pro-inflammatory activity. The presence of miR-21 inhibitor quenched the inflammatory response. This study validates the pro-inflammatory property of miR-21 with a tendency to foster an inflammatory milieu. Our findings also reinforce the dual importance of exosomal miR-21 as a biomarker and therapeutic target in inflammatory conditions.

摘要

微小 RNA 可以通过调节巨噬细胞极化来调节炎症反应。虽然 microRNA miR-21 与炎症反应中涉及的关键过程有关,但它在巨噬细胞极化中的确切作用仍存在争议。在这项研究中,我们研究了内源性 miRNA-21 的功能相关性和外泌体的作用。用 miR-21 质粒转染 RAW 264.7 巨噬细胞,通过流式细胞术、吞噬作用和实时 PCR 分析炎症细胞因子来评估炎症反应。为了了解信号通路的作用,用针对 PI3K 或 NFĸB 的特异性抑制剂处理细胞。转染细胞的外泌体用于研究 miR-21 对幼稚巨噬细胞的旁分泌作用。miR-21 的过表达导致促炎细胞因子的显著上调,使细胞向促炎表型倾斜,部分涉及 PI3K 和 NFĸB 信号通路。细胞还分泌富含 miR-21 的外泌体,将其递送到幼稚巨噬细胞中,导致它们表现出促炎活性。miR-21 抑制剂的存在抑制了炎症反应。这项研究验证了 miR-21 的促炎特性,并倾向于促进炎症环境。我们的发现还加强了外泌体 miR-21 作为炎症状态下的生物标志物和治疗靶点的双重重要性。

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Inflammation. 2021 Aug;44(4):1274-1287. doi: 10.1007/s10753-021-01415-0. Epub 2021 Jan 26.
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本文引用的文献

1
The Interplay among miRNAs, Major Cytokines, and Cancer-Related Inflammation.微小RNA、主要细胞因子与癌症相关炎症之间的相互作用
Mol Ther Nucleic Acids. 2020 Jun 5;20:606-620. doi: 10.1016/j.omtn.2020.04.002. Epub 2020 Apr 11.
2
M1 But Not M0 Extracellular Vesicles Induce Polarization of RAW264.7 Macrophages Via the TLR4-NFκB Pathway In Vitro.M1 型而非 M0 型细胞外囊泡通过 TLR4-NFκB 通路诱导 RAW264.7 巨噬细胞体外极化。
Inflammation. 2020 Oct;43(5):1611-1619. doi: 10.1007/s10753-020-01236-7.
3
Exosomal miR-21 regulates the TETs/PTENp1/PTEN pathway to promote hepatocellular carcinoma growth.
J Inflamm Res. 2024 Jul 25;17:5005-5024. doi: 10.2147/JIR.S475102. eCollection 2024.
4
miRNA-21-5p is an important contributor to the promotion of injured peripheral nerve regeneration using hypoxia-pretreated bone marrow-derived neural crest cells.微小RNA-21-5p是利用缺氧预处理的骨髓源性神经嵴细胞促进损伤周围神经再生的重要因素。
Neural Regen Res. 2025 Jan 1;20(1):277-290. doi: 10.4103/1673-5374.390956. Epub 2023 Dec 15.
5
Nrf2 Plays a Key Role in Erythropoiesis during Aging.Nrf2在衰老过程中的红细胞生成中起关键作用。
Antioxidants (Basel). 2024 Apr 12;13(4):454. doi: 10.3390/antiox13040454.
6
miR-21 Expressed by Dermal Fibroblasts Enhances Skin Wound Healing Through the Regulation of Inflammatory Cytokine Expression.由真皮成纤维细胞表达的miR-21通过调节炎性细胞因子表达促进皮肤伤口愈合。
Inflammation. 2024 Apr;47(2):572-590. doi: 10.1007/s10753-023-01930-2. Epub 2023 Dec 2.
7
The potential role of miRNA in regulating macrophage polarization.微小RNA在调节巨噬细胞极化中的潜在作用。
Heliyon. 2023 Oct 31;9(11):e21615. doi: 10.1016/j.heliyon.2023.e21615. eCollection 2023 Nov.
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Int J Mol Sci. 2023 Sep 8;24(18):13873. doi: 10.3390/ijms241813873.
9
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J Cancer Res Clin Oncol. 2023 Nov;149(17):15349-15364. doi: 10.1007/s00432-023-05313-w. Epub 2023 Aug 28.
10
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Stem Cell Rev Rep. 2023 Aug;19(6):2024-2037. doi: 10.1007/s12015-023-10560-y. Epub 2023 May 31.
外泌体 miR-21 通过调控 TETs/PTENp1/PTEN 通路促进肝癌生长。
Mol Cancer. 2019 Oct 27;18(1):148. doi: 10.1186/s12943-019-1075-2.
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Plasma exosome-encapsulated microRNA-21 and microRNA-92a are promising biomarkers for the prediction of peritoneal recurrence in patients with gastric cancer.血浆外泌体包裹的微小RNA-21和微小RNA-92a是预测胃癌患者腹膜复发的有前景的生物标志物。
Oncol Lett. 2019 Nov;18(5):4467-4480. doi: 10.3892/ol.2019.10807. Epub 2019 Sep 4.
5
MiR-21 in Substance P-induced exosomes promotes cell proliferation and migration in human colonic epithelial cells.降钙素基因相关肽诱导的外泌体中的 miR-21 促进人结肠上皮细胞的增殖和迁移。
Am J Physiol Gastrointest Liver Physiol. 2019 Dec 1;317(6):G802-G810. doi: 10.1152/ajpgi.00043.2019. Epub 2019 Sep 23.
6
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Annu Rev Pathol. 2020 Jan 24;15:123-147. doi: 10.1146/annurev-pathmechdis-012418-012718. Epub 2019 Sep 17.
7
Strategies for the use of Extracellular Vesicles for the Delivery of Therapeutics.细胞外囊泡用于治疗药物传递的策略。
J Neuroimmune Pharmacol. 2020 Sep;15(3):422-442. doi: 10.1007/s11481-019-09873-y. Epub 2019 Aug 27.
8
Macrophage-Derived miRNA-Containing Exosomes Induce Peritendinous Fibrosis after Tendon Injury through the miR-21-5p/Smad7 Pathway.巨噬细胞衍生的含miRNA外泌体通过miR-21-5p/Smad7途径在肌腱损伤后诱导腱周纤维化。
Mol Ther Nucleic Acids. 2019 Mar 1;14:114-130. doi: 10.1016/j.omtn.2018.11.006. Epub 2018 Nov 20.
9
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J Nat Med. 2019 Jan;73(1):59-66. doi: 10.1007/s11418-018-1237-3. Epub 2018 Aug 16.
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Beta cell extracellular vesicle miR-21-5p cargo is increased in response to inflammatory cytokines and serves as a biomarker of type 1 diabetes.β 细胞细胞外囊泡 miR-21-5p 载物在炎症细胞因子的刺激下增加,并作为 1 型糖尿病的生物标志物。
Diabetologia. 2018 May;61(5):1124-1134. doi: 10.1007/s00125-018-4559-5. Epub 2018 Feb 14.