原位硫醇铜复合物对巨噬细胞形态和细胞因子的再教育作用

IF 2.9 4区 医学 Q3 IMMUNOLOGY
Jorge Xool-Tamayo, Víctor Ermilo Arana-Argaez, Fabiola Villa-de la Torre, Ivan Chan-Zapata, Rossana F Vargas-Coronado, Juan V Cauich-Rodríguez
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引用次数: 0

摘要

目的:研究硫醇铜复合物对巨噬细胞形态和细胞因子表达的再教育作用:研究硫醇铜复合物对巨噬细胞形态和细胞因子表达的再教育作用:方法:通过光学显微镜观察细胞形态,评估硫醇铜复合物对小鼠巨噬细胞的影响;通过刺激后的蛋白质丰度评估细胞因子的表达。还对 PMBC 进行了存活率实验,以确认铜复合物不会影响其他细胞:结果:硫醇铜复合物在 1-200 µM 的浓度下处理后,出现了 M1 形态,而在 50 到 800 µM 的浓度下,出现了 M2 行为。令人惊讶的是,在 400-800 µM 之间观察到的细长形态与 M2 形态相似。M1 细胞因子的表达量从 1 微摩尔到 100 微摩尔不等,铜-青霉胺复合物在 1 微摩尔时产量最高(2243 pg/µL)。在 1-800 µM 的范围内观察到 M2 的产生,铜-半胱氨酸复合物的最高丰度接近 1150 pg/µL(200-400 µM)。最后,LCCu 复合物不会诱导 PBMC 产生细胞毒性反应,同时会产生大量 IL-4 和 IL-10,这与其金类似物相似:结论:硫醇铜复合物具有将 M1 形态表达重新教育为 M2 形态表达的能力,这对于使用硫醇青霉胺铜保护细胞或使用硫醇半胱氨酸铜进行组织免疫再生很有帮助。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Macrophages morphology and cytokine reeducation by ex situ copper thiol complexes.

Objective: To study the reeducation effect of copper thiol complexes on macrophage morphology and cytokine expression.

Methods: The effect of copper thiol complexes was assessed on murine macrophages by the cell morphology observed through optical microscopy, while the expression of cytokines by protein abundance after stimulation. A viability experiment was performed on PMBC to confirm that copper complexes do not affect other cells.

Results: The M1 shape was reported after treatment with copper thiol complexes at 1-200 µM, while M2 behavior was documented between 50 and 800 µM. Surprisingly, a thin elongate morphology was observed between 400-800 µM like the M2 shape. The expression of M1 cytokines was noted ranging from 1 to 100 µM, with the highest yield at 1 µM (2243 pg/µL) for the copper-penicillamine complex. M2 production behavior was observed at 1-800 µM, with the highest abundance close to 1150 pg/µL (200-400 µM) was quantified from the copper-cysteine complex. Finally, LCCu complexes did not induce a cytotoxic response on PBMC while exhibiting a high IL-4 and IL-10 production, similar to their gold analogs.

Conclusions: The capacity of copper thiol complexes to reeducate M1 to M2 morphoexpression can be promising for cell protection by using copper thiol penicillamine or immuno-regeneration of tissues when using copper thiol cysteine.

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来源期刊
CiteScore
5.40
自引率
0.00%
发文量
133
审稿时长
4-8 weeks
期刊介绍: The journal Immunopharmacology and Immunotoxicology is devoted to pre-clinical and clinical drug discovery and development targeting the immune system. Research related to the immunoregulatory effects of various compounds, including small-molecule drugs and biologics, on immunocompetent cells and immune responses, as well as the immunotoxicity exerted by xenobiotics and drugs. Only research that describe the mechanisms of specific compounds (not extracts) is of interest to the journal. The journal will prioritise preclinical and clinical studies on immunotherapy of disorders such as chronic inflammation, allergy, autoimmunity, cancer etc. The effects of small-drugs, vaccines and biologics against central immunological targets as well as cell-based therapy, including dendritic cell therapy, T cell adoptive transfer and stem cell therapy, are topics of particular interest. Publications pointing towards potential new drug targets within the immune system or novel technology for immunopharmacological drug development are also welcome. With an immunoscience focus on drug development, immunotherapy and toxicology, the journal will cover areas such as infection, allergy, inflammation, tumor immunology, degenerative disorders, immunodeficiencies, neurology, atherosclerosis and more. Immunopharmacology and Immunotoxicology will accept original manuscripts, brief communications, commentaries, mini-reviews, reviews, clinical trials and clinical cases, on the condition that the results reported are based on original, clinical, or basic research that has not been published elsewhere in any journal in any language (except in abstract form relating to paper communicated to scientific meetings and symposiums).
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