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首页> 外文期刊>Bulletin of experimental biology and medicine >Alteraatife Reprogrammlig of M1/M2 Pheiotype of Mouse Peritoneal Macrophages In Vitro with Interferon-gamma and Interleukin-4
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Alteraatife Reprogrammlig of M1/M2 Pheiotype of Mouse Peritoneal Macrophages In Vitro with Interferon-gamma and Interleukin-4

机译:小鼠腹膜巨噬细胞M1 / M2表型与干扰素-γ和白介素4体外的Alteraatife重编程。

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摘要

An important role in the development of the immune response is played by macrophages that acquire either anti-inflammatory Ml or anti-inflammatory M2 phenotype depending on their microenvironment. The possibility of targeted reprogramming of the initial M2 macrophage phenotype towards Ml phenotype and vice versa using macrophage reprogramming factors IFN-y and IL-4, respectively, was demonstrated. We showed that macrophages of genetically different mouse strains did not practically differ by their reprogramming capacity. Our findings suggest that macrophage programming not only participates in the triggering of the immune response, but also can ensure plasticity of functional activity during the developing response.
机译:巨噬细胞在免疫应答的发展中起重要作用,巨噬细胞根据其微环境获得抗炎M1或抗炎M2表型。证明了分别使用巨噬细胞重编程因子IFN-γ和IL-4有针对性地将初始M2巨噬细胞表型向M1表型进行反编程的可能性,反之亦然。我们表明,遗传上不同的小鼠品系的巨噬细胞实际上没有通过其重编程能力的差异。我们的发现表明,巨噬细胞程序设计不仅参与免疫应答的触发,而且还可以确保发育应答过程中功能活性的可塑性。

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