
Mitochondrial arginase-2 is essential for IL-10 metabolic ... - Nature
2021年3月5日 · Here, we show that arginase-2 (Arg2) is a microRNA-155 (miR-155) and interleukin-10 (IL-10) regulated protein localized at the mitochondria in inflammatory macrophages, and is critical for...
巨噬细胞极化标志物 - 知乎 - 知乎专栏
2023年12月26日 · m2巨噬细胞的主要标记是 cd163 和cd206。此外,精氨酸酶1(arg1)和dectin-1也是用于鉴定m2巨噬细胞的理想表型指标。 研究还显示,fizz1、ym1和ly6c 也可以用作与m1或m2巨噬细胞亚群相关的表面标记。
Inhibition of pro-inflammatory signaling in human primary …
2023年9月12日 · We have previously shown that arginase-2 (Arg2), a mitochondrial enzyme, is a key regulator of the macrophage anti-inflammatory response. Here, we investigate the therapeutic potential of Arg2 enhancement via target site blockers (TSBs) in human macrophages.
Functions of Arginase Isoforms in Macrophage Inflammatory Responses ...
2021年10月27日 · The M1 killer type response and the M2 repair type response are best known, and are two extreme examples. Among other markers, inducible nitric oxide synthase and type-I arginase (Arg-I), the enzymes that are involved in l -arginine/nitric oxide (NO) metabolism, are associated with the M1 and M2 phenotype, respectively, and therefore widely ...
线粒体精氨酸酶 2 对炎症巨噬细胞的 IL-10 代谢重编程至关重 …
Here, we show that arginase-2 (Arg2) is a microRNA-155 (miR-155) and interleukin-10 (IL-10) regulated protein localized at the mitochondria in inflammatory macrophages, and is critical for IL-10-induced modulation of mitochondrial dynamics and oxidative respiration.
Polarization of Macrophages toward M2 Phenotype Is Favored by …
Our findings of higher Arg1 and blunted induction of Arg2 in the iPLA 2 β −/−, relative to WT macrophages support the possibility that Arg2 is a proinflammatory marker under classical activation conditions, as might exist in an in vivo inflammatory milieu such as T1D.
Arginase: shedding light on the mechanisms and opportunities in ...
2022年10月8日 · ARG1 promotes M2 anti-inflammation response through blocking NO production from iNOS, but ARG2 induces pro-inflammatory cytokine production (TNF-α, IL-6, and MCP-1) in M1 via mitochondrial ROS...
Cell Reports 丨M1&M2 巨噬细胞极化的转换 - 知乎 - 知乎专栏
2023年6月14日 · 尽管 Arg1 基因表达是可塑的,并且在 LPS + IFNγ 刺激后仍可被 IL-4 诱导(图 1B),但与 M2 细胞相比,M1→M2 巨噬细胞显示出明显较少的 IL-4 诱导的精氨酸酶功能(图 1D)。 同样,LPS + IFNγ 预处理损害了 IL-10 引发的 M2 样表型的诱导。 接下来,作者通过比较 LPS + IFNγ 诱导的 M2→M1 反应与正常 M1 细胞(红色)的反应,研究了 M2 巨噬细胞产生炎症反应的能力。 作者发现,与第一次刺激无关,LPS + IFNγ 在 M2→M1 和 M1 细胞中有效诱导 …
Mitochondrial arginase-2 is essential for IL-10 metabolic …
Here, we show that arginase-2 (Arg2) is a microRNA-155 (miR-155) and interleukin-10 (IL-10) regulated protein localized at the mitochondria in inflammatory macrophages, and is critical for IL-10-induced modulation of mitochondrial dynamics and oxidative respiration.
Mitochondrial arginase-2 is essential for IL-10 metabolic ... - PubMed
2021年3月5日 · Here, we show that arginase-2 (Arg2) is a microRNA-155 (miR-155) and interleukin-10 (IL-10) regulated protein localized at the mitochondria in inflammatory macrophages, and is critical for IL-10-induced modulation of mitochondrial dynamics and …