电刺激对细胞因子诱导的巨噬细胞极化的影响

IF 3.1 3区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Journal of Tissue Engineering and Regenerative Medicine Pub Date : 2022-02-28 DOI:10.1002/term.3292
Jiahao Gu, Xuzhao He, Xiaoyi Chen, Lingqing Dong, Wenjian Weng, Kui Cheng
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引用次数: 9

摘要

巨噬细胞具有M1和M2两种功能化表型,巨噬细胞M1/M2极化的调节对组织修复至关重要。组织源性免疫因子被认为是巨噬细胞极化的主要驱动因素。基于细胞因子诱导的主要极化途径,我们测试了巨噬细胞电刺激(ES)对M1/M2极化的调节作用以及可能与细胞因子的协同作用。采用氧化铟锡(ITO)平面微电极在不同电压、频率和波形下制备ES。我们利用脂多糖(LPS)/IFN-γ因子和IL-4因子分别培养的小鼠骨髓源性巨噬细胞,评估ES对细胞因子诱导的M1/M2极化的影响。结果表明,ES促进了细胞因子诱导的巨噬细胞极化。重要的是,我们发现方形波形刺激选择性地促进了LPS/IFN-γ诱导的M1极化,而正弦波形刺激同时促进了LPS/IFN-γ诱导的M1和il -4诱导的M2极化。在机制上,方形波形刺激影响细胞内离子浓度,而正弦波形刺激促进细胞内离子浓度和膜受体。我们在此建立es介导的巨噬细胞极化免疫调节策略。
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Effects of electrical stimulation on cytokine-induced macrophage polarization

Macrophages have two functionalized phenotypes, M1 and M2, and the regulation of M1/M2 polarization of macrophages is critical for tissue repair. Tissue-derived immune factors are considered the major drivers of macrophage polarization. Based on the main cytokine-induced polarization pathways, we tested the effect of electrical stimulation (ES) of macrophages on the regulation of M1/M2 polarization and a possible synergistic effect with the cytokines. Indium tin oxide (ITO) planar microelectrodes were used to produce ES under different voltages, frequencies and waveforms. We evaluated the influence of ES on the cytokine-induced M1/M2 polarization using mouse bone marrow-derived macrophages cultured with both lipopolysaccharide (LPS)/IFN-γ factors and IL-4 factors for M1 and M2, respectively. The results showed that ES promoted the cytokine-induced macrophage polarization. Importantly, we found that stimulation with a square waveform selectively promoted LPS/IFN-γ-induced M1 polarization, while stimulation with a sinusoidal waveform promoted both LPS/IFN-γ-induced M1, and IL-4-induced M2 polarization. Mechanistically, stimulation with a square waveform affected the intracellular ion concentration, whereas stimulation with a sinusoidal waveform promoted both the intracellular ion concentration and membrane receptors. We hereby establish an ES-mediated strategy for immunomodulation via macrophage polarization.

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来源期刊
CiteScore
7.50
自引率
3.00%
发文量
97
审稿时长
4-8 weeks
期刊介绍: Journal of Tissue Engineering and Regenerative Medicine publishes rapidly and rigorously peer-reviewed research papers, reviews, clinical case reports, perspectives, and short communications on topics relevant to the development of therapeutic approaches which combine stem or progenitor cells, biomaterials and scaffolds, growth factors and other bioactive agents, and their respective constructs. All papers should deal with research that has a direct or potential impact on the development of novel clinical approaches for the regeneration or repair of tissues and organs. The journal is multidisciplinary, covering the combination of the principles of life sciences and engineering in efforts to advance medicine and clinical strategies. The journal focuses on the use of cells, materials, and biochemical/mechanical factors in the development of biological functional substitutes that restore, maintain, or improve tissue or organ function. The journal publishes research on any tissue or organ and covers all key aspects of the field, including the development of new biomaterials and processing of scaffolds; the use of different types of cells (mainly stem and progenitor cells) and their culture in specific bioreactors; studies in relevant animal models; and clinical trials in human patients performed under strict regulatory and ethical frameworks. Manuscripts describing the use of advanced methods for the characterization of engineered tissues are also of special interest to the journal readership.
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