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本文引用的文献

1
Membrane recognition by phospholipid-binding domains.磷脂结合结构域对膜的识别
Nat Rev Mol Cell Biol. 2008 Feb;9(2):99-111. doi: 10.1038/nrm2328.
2
A selective PIKfyve inhibitor blocks PtdIns(3,5)P(2) production and disrupts endomembrane transport and retroviral budding.一种选择性PIKfyve抑制剂可阻断磷脂酰肌醇-3,5-二磷酸(PtdIns(3,5)P(2))的生成,并破坏内膜运输和逆转录病毒出芽。
EMBO Rep. 2008 Feb;9(2):164-70. doi: 10.1038/sj.embor.7401155. Epub 2008 Jan 11.
3
Membrane phosphatidylserine regulates surface charge and protein localization.膜磷脂酰丝氨酸调节表面电荷和蛋白质定位。
Science. 2008 Jan 11;319(5860):210-3. doi: 10.1126/science.1152066.
4
Engulfment of apoptotic cells: signals for a good meal.凋亡细胞的吞噬:美餐的信号。
Nat Rev Immunol. 2007 Dec;7(12):964-74. doi: 10.1038/nri2214.
5
The dynamic phagosomal proteome and the contribution of the endoplasmic reticulum.动态吞噬体蛋白质组及内质网的作用
Proc Natl Acad Sci U S A. 2007 Nov 20;104(47):18520-5. doi: 10.1073/pnas.0705801104. Epub 2007 Nov 15.
6
Cholesterol level regulates endosome motility via Rab proteins.胆固醇水平通过Rab蛋白调节内体运动。
Biophys J. 2008 Feb 15;94(4):1508-20. doi: 10.1529/biophysj.106.099366. Epub 2007 Nov 2.
7
Rapid cell corpse clearance by stabilin-2, a membrane phosphatidylserine receptor.膜磷脂酰丝氨酸受体stabilin-2介导的快速细胞尸体清除
Cell Death Differ. 2008 Jan;15(1):192-201. doi: 10.1038/sj.cdd.4402242. Epub 2007 Oct 26.
8
Identification of Tim4 as a phosphatidylserine receptor.鉴定Tim4为磷脂酰丝氨酸受体。
Nature. 2007 Nov 15;450(7168):435-9. doi: 10.1038/nature06307. Epub 2007 Oct 24.
9
BAI1 is an engulfment receptor for apoptotic cells upstream of the ELMO/Dock180/Rac module.BAI1是ELMO/Dock180/Rac模块上游凋亡细胞的吞噬受体。
Nature. 2007 Nov 15;450(7168):430-4. doi: 10.1038/nature06329.
10
Wiskott-Aldrich syndrome protein is a key regulator of the phagocytic cup formation in macrophages.威斯科特-奥尔德里奇综合征蛋白是巨噬细胞中吞噬杯形成的关键调节因子。
J Biol Chem. 2007 Nov 23;282(47):34194-203. doi: 10.1074/jbc.M705999200. Epub 2007 Sep 21.

病原体破坏与细胞内存活:脂质作为吞噬体命运决定因素的作用

Pathogen destruction versus intracellular survival: the role of lipids as phagosomal fate determinants.

作者信息

Steinberg Benjamin E, Grinstein Sergio

机构信息

Program in Cell Biology, Hospital for Sick Children, Institute of Medical Science and Department of Biochemistry, University of Toronto, Toronto, Ontario, Canada.

出版信息

J Clin Invest. 2008 Jun;118(6):2002-11. doi: 10.1172/JCI35433.

DOI:10.1172/JCI35433
PMID:18523652
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2396921/
Abstract

Phagocytosis is a key component of the innate immune response and of the clearance of apoptotic bodies. Phagosome formation and subsequent maturation require extensive cytoskeletal rearrangement and precisely choreographed vesicular fusion and fission events. The objectives of this review are to highlight the functional importance of lipids in the phagocytic process, to discuss how pathogenic microorganisms can in some cases manipulate host lipid metabolism to either co-opt or disrupt phagosome maturation and promote their own survival, and to describe how defective phagosomal lipid metabolism can result in disease.

摘要

吞噬作用是固有免疫反应和凋亡小体清除的关键组成部分。吞噬体的形成及随后的成熟需要广泛的细胞骨架重排以及精确编排的囊泡融合与裂变事件。本综述的目的是强调脂质在吞噬过程中的功能重要性,讨论致病微生物在某些情况下如何操纵宿主脂质代谢以要么利用要么破坏吞噬体成熟并促进自身存活,以及描述吞噬体脂质代谢缺陷如何导致疾病。