Résumé
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 phos-phoinositide plays important roles during the maturation of the phagosome.
Langue d'origine | English |
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Pages (de-à) | 128-140 |
Nombre de pages | 13 |
Journal | Molecular Biology of the Cell |
Volume | 28 |
Numéro de publication | 1 |
DOI | |
Statut de publication | Published - janv. 1 2017 |
Publié à l'externe | Oui |
Note bibliographique
Funding Information:R.L. is funded by the Connaught International Scholarship for Doctoral Students from the University of Toronto and by the National Council for Science and Technology/Consejo Nacional de Ciencia y Tecnologia of Mexico. This work was supported by Grant FDN-143202 from the Canadian Institutes of Health Research to S.G., Grant MOP-133656 from the Canadian Institutes of Health Research to G.D.F., funds from the Department of Cell Biology, University of Pittsburgh School of Medicine, to G.H., the intramural program of the Eunice Kennedy Shriver National Institute of Child Health and Human Development of the National Institutes of Health to T.B., and Grant DK082700 from the National Institutes of Health to P.D.C.
Publisher Copyright:
© 2017 Levin et al.
ASJC Scopus Subject Areas
- Molecular Biology
- Cell Biology
PubMed: MeSH publication types
- Journal Article
- Research Support, N.I.H., Extramural
- Research Support, Non-U.S. Gov't
- Research Support, N.I.H., Intramural