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Scrib 和Dlg1 极性蛋白调节人类树突状细胞中的 Ag 呈递。

Scrib and Dlg1 polarity proteins regulate Ag presentation in human dendritic cells.

机构信息

Laboratory of Autoimmunity, Instituto Nacional de Enfermedades Respiratorias Ismael Cosío Villegas, Mexico City, Mexico.

Departamento de Inmunología, Escuela Nacional de Ciencias Biológicas, Instituto Politécnico Nacional, ENCB-IPN, Ciudad de México, México.

出版信息

J Leukoc Biol. 2020 Sep;108(3):883-893. doi: 10.1002/JLB.4MA0320-544RR. Epub 2020 Apr 15.

Abstract

We recently reported, for the first time, the expression and regulation of the PDZ polarity proteins Scrib and Dlg1 in human APCs, and also described the viral targeting of these proteins by NS1 of influenza A virus in human dendritic cells (DCs). Scrib plays an important role in reactive oxygen species (ROS) production in Mϕs and uropod formation and migration in T cells, while Dlg1 is important for T cell downstream activation after Ag recognition. Nevertheless, the functions of these proteins in human DCs remain unknown. Here, we knocked-down the expression of both Scrib and Dlg1 in human DCs and then evaluated the expression of co-stimulatory molecules and cytokine production during maturation. We demonstrated that Scrib is necessary for adequate CD86 expression, while Dlg1 is important for CD83 up-regulation and IL-6 production upon maturation, suggesting that Scrib and Dlg1 participate in separate pathways in DCs. Additionally, both proteins are required for adequate IL-12 production after maturation. Furthermore, we showed that the inefficient maturation of DCs induced by Scrib or Dlg1 depletion leads to impaired T cell activation. Our results revealed the previously unknown contribution of Scrib and Dlg1 in human DCs pivotal functions, which may be able to impact innate and adaptive immune response.

摘要

我们最近首次报道了 PDZ 极性蛋白 Scrib 和 Dlg1 在人 APC 中的表达和调节,还描述了流感 A 病毒 NS1 对人树突状细胞(DC)中这些蛋白的病毒靶向作用。Scrib 在 Mϕs 中活性氧(ROS)的产生和 T 细胞中足突的形成和迁移中发挥重要作用,而 Dlg1 对 Ag 识别后 T 细胞的下游激活很重要。然而,这些蛋白在人 DC 中的功能仍不清楚。在这里,我们敲低了人 DC 中 Scrib 和 Dlg1 的表达,然后评估了成熟过程中共刺激分子的表达和细胞因子的产生。我们证明 Scrib 对于 CD86 的充分表达是必需的,而 Dlg1 对于 CD83 的上调和成熟时 IL-6 的产生很重要,这表明 Scrib 和 Dlg1 参与了 DC 中的不同途径。此外,这两种蛋白对于成熟后 IL-12 的充分产生也是必需的。此外,我们表明 Scrib 或 Dlg1 耗尽诱导的 DC 成熟不良会导致 T 细胞激活受损。我们的结果揭示了 Scrib 和 Dlg1 在人 DCs 中以前未知的重要功能的贡献,这可能会影响固有和适应性免疫反应。

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