Centre for Immune Regulation, Department of Biosciences, University of Oslo, Oslo, Norway.
PLoS One. 2013 Sep 5;8(9):e73538. doi: 10.1371/journal.pone.0073538. eCollection 2013.
The regulation of Rab expression to modulate cellular function has recently been proposed. Dendritic cells are a prototypic example of cells that drastically alter their function in response to environmental cues by reducing endocytosis, secreting cytokines, changing surface protein repertoires and altering morphology and migration. This is not a binary event, but is subject to fluctuations through the activation process, termed maturation. Consequently, DCs transiently increase endocytosis and production of major histocompatibility complex class II molecules, and secrete inflammatory cytokines in infected tissues before migrating to secondary lymph nodes and releasing T cell polarizing factors. All these cellular processes rely on intracellular membrane transport, which is regulated by Rab family GTPases and their diverse effectors. Here we examine how the Rabs likely to be involved in these functions are regulated throughout DC maturation. We find that Rab expression is altered upon lipopolysaccharide-induced activation, and discuss how this correlates to the reported functions of these cells during maturation.
最近有人提出,通过调节 Rab 表达来调节细胞功能。树突状细胞是一个典型的例子,它们通过降低内吞作用、分泌细胞因子、改变表面蛋白谱以及改变形态和迁移来响应环境线索,从而极大地改变其功能。这不是一个二元事件,而是通过激活过程(称为成熟)而发生波动。因此,DC 在迁移到次级淋巴节点并释放 T 细胞极化因子之前,会短暂增加内吞作用和主要组织相容性复合体 II 类分子的产生,并在感染组织中分泌炎症细胞因子。所有这些细胞过程都依赖于细胞内的膜转运,而这是由 Rab 家族 GTPases 及其不同的效应物调节的。在这里,我们研究了在 DC 成熟过程中,可能参与这些功能的 Rab 是如何被调节的。我们发现 Rab 的表达在脂多糖诱导的激活后发生改变,并讨论了这与这些细胞在成熟过程中的报告功能有何关联。