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Dev Cell. 2012 Jun 12;22(6):1313-20. doi: 10.1016/j.devcel.2012.04.007. Epub 2012 May 31.
2
The intracellular region of Notch ligands Dll1 and Dll3 regulates their trafficking and signaling activity.Notch配体Dll1和Dll3的细胞内区域调节它们的运输和信号传导活性。
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3
Notch ligand endocytosis generates mechanical pulling force dependent on dynamin, epsins, and actin.Notch 配体内吞作用产生依赖于胞质动力蛋白、衔接蛋白和肌动蛋白的机械牵拉力。
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Dynamic Ligand Discrimination in the Notch Signaling Pathway. Notch 信号通路中的动态配体识别。
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Notch1 endocytosis is induced by ligand and is required for signal transduction.Notch1内吞作用由配体诱导,是信号转导所必需的。
Biochim Biophys Acta. 2016 Jan;1863(1):166-77. doi: 10.1016/j.bbamcr.2015.10.021. Epub 2015 Oct 30.

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The Clathrin adaptor AP-1 and Stratum act in parallel pathways to control Notch activation in sensory organ precursors cells.网格蛋白衔接蛋白 AP-1 和 Stratum 在平行途径中协同作用,以控制感觉器官前体细胞中 Notch 的激活。
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Probing Ligand-Receptor Interaction in Living Cells Using Force Measurements With Optical Tweezers.利用光镊进行力测量来探究活细胞中的配体-受体相互作用
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本文引用的文献

1
Notch ligand endocytosis generates mechanical pulling force dependent on dynamin, epsins, and actin.Notch 配体内吞作用产生依赖于胞质动力蛋白、衔接蛋白和肌动蛋白的机械牵拉力。
Dev Cell. 2012 Jun 12;22(6):1299-312. doi: 10.1016/j.devcel.2012.04.005. Epub 2012 May 31.
2
Concentration independent modulation of local micromechanics in a fibrin gel.纤维蛋白凝胶中局部微观力学的浓度非依赖性调制。
PLoS One. 2011;6(5):e20201. doi: 10.1371/journal.pone.0020201. Epub 2011 May 23.
3
The functions of auxilin and Rab11 in Drosophila suggest that the fundamental role of ligand endocytosis in notch signaling cells is not recycling.auxilin 和 Rab11 在果蝇中的功能表明,配体内吞作用在 Notch 信号细胞中的基本作用不是再循环。
PLoS One. 2011 Mar 23;6(3):e18259. doi: 10.1371/journal.pone.0018259.
4
Canonical and non-canonical Notch ligands.经典和非经典 Notch 配体。
Curr Top Dev Biol. 2010;92:73-129. doi: 10.1016/S0070-2153(10)92003-6.
5
Cis-interactions between Notch and Delta generate mutually exclusive signalling states.Notch 和 Delta 之间的顺式相互作用产生相互排斥的信号状态。
Nature. 2010 May 6;465(7294):86-90. doi: 10.1038/nature08959. Epub 2010 Apr 25.
6
Neuralized promotes basal to apical transcytosis of delta in epithelial cells.神经化促进上皮细胞中德尔塔的基底到顶质的胞吞作用。
Mol Biol Cell. 2010 Jun 15;21(12):2078-86. doi: 10.1091/mbc.e09-11-0926. Epub 2010 Apr 21.
7
Endocytic internalization routes required for delta/notch signaling.德尔塔/Notch 信号传导所需的内吞内化途径。
Curr Biol. 2010 Mar 23;20(6):538-43. doi: 10.1016/j.cub.2010.01.049. Epub 2010 Mar 11.
8
Coordinated actions of actin and BAR proteins upstream of dynamin at endocytic clathrin-coated pits.网格蛋白包被陷窝内肌动蛋白和 BAR 蛋白上游的动力蛋白协调作用。
Dev Cell. 2009 Dec;17(6):811-22. doi: 10.1016/j.devcel.2009.11.005.
9
Embryonic arrest at midgestation and disruption of Notch signaling produced by the absence of both epsin 1 and epsin 2 in mice.小鼠中由于 epsin 1 和 epsin 2 均缺失导致妊娠中期胚胎停滞以及 Notch 信号通路中断。
Proc Natl Acad Sci U S A. 2009 Aug 18;106(33):13838-43. doi: 10.1073/pnas.0907008106. Epub 2009 Aug 5.
10
The Arp2/3 complex and WASp are required for apical trafficking of Delta into microvilli during cell fate specification of sensory organ precursors.在感觉器官前体细胞命运特化过程中,Arp2/3复合物和WASp是Delta顶端运输到微绒毛所必需的。
Nat Cell Biol. 2009 Jul;11(7):815-24. doi: 10.1038/ncb1888. Epub 2009 Jun 21.

光学镊子研究 Notch:单分子相互作用强度与配体内吞无关。

Optical tweezers studies on Notch: single-molecule interaction strength is independent of ligand endocytosis.

机构信息

Department of Biomedical Engineering, UCI, Irvine, CA 92612, USA.

出版信息

Dev Cell. 2012 Jun 12;22(6):1313-20. doi: 10.1016/j.devcel.2012.04.007. Epub 2012 May 31.

DOI:10.1016/j.devcel.2012.04.007
PMID:22658935
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3376165/
Abstract

Notch signaling controls diverse cellular processes critical to development and disease. Cell surface ligands bind Notch on neighboring cells but require endocytosis to activate signaling. The role ligand endocytosis plays in Notch activation has not been established. Here we integrate optical tweezers with cell biological and biochemical methods to test the prevailing model that ligand endocytosis facilitates recycling to enhance ligand interactions with Notch necessary to trigger signaling. Specifically, single-molecule measurements indicate that interference of ligand endocytosis and/or recycling does not alter the force required to rupture bonds formed between cells expressing the Notch ligand Delta-like1 (Dll1) and laser-trapped Notch1 beads. Together, our analyses eliminate roles for ligand endocytosis and recycling in Dll1-Notch1 interactions and indicate that recycling indirectly affects signaling by regulating the accumulation of cell surface ligand. Importantly, our study demonstrates the utility of optical tweezers to test a role for ligand endocytosis in generating cell-mediated mechanical force.

摘要

Notch 信号通路控制着许多对发育和疾病至关重要的细胞过程。细胞表面配体与相邻细胞上的 Notch 结合,但需要内吞作用才能激活信号通路。配体内吞作用在 Notch 激活中的作用尚未确定。在这里,我们将光学镊子与细胞生物学和生化方法相结合,以测试目前的模型,即配体内吞作用有助于循环,从而增强与 Notch 的配体相互作用,从而触发信号转导。具体而言,单分子测量表明,干扰配体的内吞作用和/或循环不会改变在表达 Notch 配体 Delta-like1 (Dll1) 的细胞和激光捕获的 Notch1 珠之间形成的键断裂所需的力。综上所述,我们的分析排除了配体内吞作用和循环在 Dll1-Notch1 相互作用中的作用,并表明循环通过调节细胞表面配体的积累间接影响信号转导。重要的是,我们的研究证明了光学镊子在测试配体内吞作用在产生细胞介导的机械力中的作用的实用性。