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PI3K 与趋化性:启动问题?

PI3K and chemotaxis: a priming issue?

机构信息

Laboratory of Cellular and Molecular Biology, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, USA.

出版信息

Sci Signal. 2011 Apr 26;4(170):pe22. doi: 10.1126/scisignal.2002019.

DOI:10.1126/scisignal.2002019
PMID:21521877
Abstract

Although the spatiotemporal activation of phosphoinositide 3-kinases (PI3Ks) at the leading edge of chemotaxing cells represents a key marker of polarity, both Dictyostelium discoideum and neutrophils lacking measurable PI3K activity can still migrate directionally under certain conditions. Evidence from various papers suggests that the differentiation state of cells or their priming status can consolidate otherwise contradictory findings.

摘要

尽管磷酸肌醇 3-激酶(PI3Ks)在趋化细胞前缘的时空激活代表了极性的一个关键标志,但在某些条件下,缺乏可测量 PI3K 活性的 Dictyostelium discoideum 和中性粒细胞仍然可以定向迁移。来自不同论文的证据表明,细胞的分化状态或其初始状态可以整合其他相互矛盾的发现。

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1
PI3K and chemotaxis: a priming issue?PI3K 与趋化性:启动问题?
Sci Signal. 2011 Apr 26;4(170):pe22. doi: 10.1126/scisignal.2002019.
2
Spatial regulation of PI3K signaling during chemotaxis.在趋化作用过程中 PI3K 信号的空间调节。
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Signaling pathways mediating chemotaxis in the social amoeba, Dictyostelium discoideum.介导社会变形虫盘基网柄菌趋化性的信号通路。
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Chemoattractants and chemorepellents act by inducing opposite polarity in phospholipase C and PI3-kinase signaling.化学引诱剂和化学排斥剂通过在磷脂酶C和PI3激酶信号传导中诱导相反的极性来发挥作用。
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Signaling pathways at the leading edge of chemotaxing cells.趋化细胞前沿的信号通路。
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Moving toward understanding eukaryotic chemotaxis.迈向对真核生物趋化性的理解。
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Receptor-mediated regulation of PI3Ks confines PI(3,4,5)P3 to the leading edge of chemotaxing cells.受体介导的PI3K调节将PI(3,4,5)P3限制在趋化细胞的前沿。
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Spatial and temporal regulation of 3-phosphoinositides by PI 3-kinase and PTEN mediates chemotaxis.PI 3激酶和PTEN对3-磷酸肌醇的时空调节介导趋化作用。
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Making all the right moves: chemotaxis in neutrophils and Dictyostelium.做出所有正确的行动:中性粒细胞和盘基网柄菌中的趋化作用。
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引用本文的文献

1
A meta-analysis indicates that the regulation of cell motility is a non-intrinsic function of chemoattractant receptors that is governed independently of directional sensing.一项荟萃分析表明,趋化因子受体对细胞迁移的调节是一种非固有功能,它独立于定向感应进行调控。
Front Immunol. 2022 Oct 20;13:1001086. doi: 10.3389/fimmu.2022.1001086. eCollection 2022.
2
Phosphoinositide-3-Kinase γ Is Not a Predominant Regulator of ATP-Dependent Directed Microglial Process Motility or Experience-Dependent Ocular Dominance Plasticity.磷酸肌醇-3-激酶 γ 不是 ATP 依赖性定向小胶质细胞运动或经验依赖性眼优势可塑性的主要调节剂。
eNeuro. 2020 Oct 16;7(6). doi: 10.1523/ENEURO.0311-20.2020. Print 2020 Nov-Dec.
3
A RAB35-p85/PI3K axis controls oscillatory apical protrusions required for efficient chemotactic migration.
RAB35-p85/PI3K 轴控制着高效趋化性迁移所需的振荡顶端突起。
Nat Commun. 2018 Apr 16;9(1):1475. doi: 10.1038/s41467-018-03571-8.
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PKN1 Directs Polarized RAB21 Vesicle Trafficking via RPH3A and Is Important for Neutrophil Adhesion and Ischemia-Reperfusion Injury.PKN1通过RPH3A指导极化的RAB21囊泡运输,对中性粒细胞黏附和缺血再灌注损伤很重要。
Cell Rep. 2017 Jun 20;19(12):2586-2597. doi: 10.1016/j.celrep.2017.05.080.
5
Neutrophil migration in infection and wound repair: going forward in reverse.中性粒细胞在感染和伤口修复中的迁移:逆向前行。
Nat Rev Immunol. 2016 May 27;16(6):378-91. doi: 10.1038/nri.2016.49.
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Locally excitable Cdc42 signals steer cells during chemotaxis.局部可兴奋的Cdc42信号在趋化作用过程中引导细胞。
Nat Cell Biol. 2016 Feb;18(2):191-201. doi: 10.1038/ncb3292. Epub 2015 Dec 21.
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Evolutionary history of phosphatidylinositol- 3-kinases: ancestral origin in eukaryotes and complex duplication patterns.磷脂酰肌醇-3-激酶的进化史:真核生物中的祖先起源及复杂的复制模式
BMC Evol Biol. 2015 Oct 19;15:226. doi: 10.1186/s12862-015-0498-7.
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Chemical synthesis of a two-photon-activatable chemokine and photon-guided lymphocyte migration in vivo.双光子可激活趋化因子的化学合成及体内光子引导的淋巴细胞迁移
Nat Commun. 2015 May 26;6:7220. doi: 10.1038/ncomms8220.
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Effects of isoform-selective phosphatidylinositol 3-kinase inhibitors on osteoclasts: actions on cytoskeletal organization, survival, and resorption.同工型选择性磷脂酰肌醇 3-激酶抑制剂对破骨细胞的影响:对细胞骨架组织、存活和吸收的作用。
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Role of inositol poly-phosphatases and their targets in T cell biology.肌醇多磷酸酶及其靶点在T细胞生物学中的作用。
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