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吞噬作用过程中磷脂酰肌醇4-磷酸的多相动力学

Multiphasic dynamics of phosphatidylinositol 4-phosphate during phagocytosis.

作者信息

Levin Roni, Hammond Gerald R V, Balla Tamas, De Camilli Pietro, Fairn Gregory D, Grinstein Sergio

机构信息

Division of Cell Biology, Hospital for Sick Children, Toronto, ON M5G 1X8, Canada.

Department of Biochemistry, University of Toronto, Toronto, ON M5S 1A8, Canada.

出版信息

Mol Biol Cell. 2017 Jan 1;28(1):128-140. doi: 10.1091/mbc.E16-06-0451. Epub 2016 Nov 9.

Abstract

We analyzed the distribution, fate, and functional role of phosphatidylinositol 4-phosphate (PtdIns4P) during phagosome formation and maturation. To this end, we used genetically encoded probes consisting of the PtdIns4P-binding domain of the bacterial effector SidM. PtdIns4P was found to undergo complex, multiphasic changes during phagocytosis. The phosphoinositide, which is present in the plasmalemma before engagement of the target particle, is transiently enriched in the phagosomal cup. Soon after the phagosome seals, PtdIns4P levels drop precipitously due to the hydrolytic activity of Sac2 and phospholipase C, becoming undetectable for ∼10 min. PtdIns4P disappearance coincides with the emergence of phagosomal PtdIns3P. Conversely, the disappearance of PtdIns3P that signals the transition from early to late phagosomes is accompanied by resurgence of PtdIns4P, which is associated with the recruitment of phosphatidylinositol 4-kinase 2A. The reacquisition of PtdIns4P can be prevented by silencing expression of the kinase and can be counteracted by recruitment of a 4-phosphatase with a heterodimerization system. Using these approaches, we found that the secondary accumulation of PtdIns4P is required for proper phagosomal acidification. Defective acidification may be caused by impaired recruitment of Rab7 effectors, including RILP, which were shown earlier to displace phagosomes toward perinuclear lysosomes. Our results show multimodal dynamics of PtdIns4P during phagocytosis and suggest that the phosphoinositide plays important roles during the maturation of the phagosome.

摘要

我们分析了磷脂酰肌醇4-磷酸(PtdIns4P)在吞噬体形成和成熟过程中的分布、去向及功能作用。为此,我们使用了由细菌效应蛋白SidM的PtdIns4P结合结构域组成的基因编码探针。研究发现,PtdIns4P在吞噬过程中经历复杂的多阶段变化。在靶颗粒结合之前存在于质膜中的磷酸肌醇会在吞噬体杯状结构中短暂富集。吞噬体封闭后不久,由于Sac2和磷脂酶C的水解活性,PtdIns4P水平急剧下降,在约10分钟内变得无法检测到。PtdIns4P的消失与吞噬体PtdIns3P的出现同时发生。相反,标志着从早期吞噬体向晚期吞噬体转变的PtdIns3P的消失伴随着PtdIns4P的重新出现,这与磷脂酰肌醇4激酶2A的募集有关。通过沉默激酶的表达可以阻止PtdIns4P的重新获得,并且可以通过异二聚化系统募集4-磷酸酶来抵消这种现象。使用这些方法,我们发现PtdIns4P的二次积累是吞噬体正常酸化所必需的。酸化缺陷可能是由于Rab7效应蛋白(包括RILP)的募集受损所致,先前已表明这些效应蛋白会将吞噬体移向核周溶酶体。我们的结果显示了吞噬过程中PtdIns4P的多模式动态变化,并表明磷酸肌醇在吞噬体成熟过程中发挥重要作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1aa1/5221617/9eb6d1b2e46a/128fig1.jpg

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