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一种用于三维核重建的多功能图像分析平台。

A versatile image analysis platform for three-dimensional nuclear reconstruction.

机构信息

Department of Cell Biology, Yale School of Medicine, 333 Cedar Street, New Haven, CT 06520, USA.

Department of Physics, Department of Applied Physics, Yale University, 217 Prospect Street, New Haven, CT 06511, USA.

出版信息

Methods. 2019 Mar 15;157:15-27. doi: 10.1016/j.ymeth.2018.10.009. Epub 2018 Oct 22.

DOI:10.1016/j.ymeth.2018.10.009
PMID:30359725
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6401273/
Abstract

Nuclear morphology is indicative of cellular health in many contexts. In order to robustly and quantitatively measure nuclear size and shape, numerous experimental methods leveraging fluorescence microscopy have been developed. While these methods are useful for quantifying two-dimensional morphology, they often fail to accurately represent the three-dimensional structure of the nucleus, thus omitting important spatial and volumetric information. To address the need for a more accurate image analysis modality, we have developed a software platform that faithfully reconstructs membrane surfaces in three dimensions with sub-pixel resolution. Here, we showcase its broad applicability across species and nuclear scale, as well as provide information on how to employ this platform for diverse experimental systems.

摘要

核形态在许多情况下都能反映细胞的健康状况。为了稳健且定量地测量核的大小和形状,已经开发出了许多利用荧光显微镜的实验方法。虽然这些方法对于量化二维形态很有用,但它们往往无法准确表示核的三维结构,从而遗漏了重要的空间和体积信息。为了解决更准确的图像分析模式的需求,我们开发了一个软件平台,该平台能够以亚像素分辨率忠实重建三维的膜表面。在这里,我们展示了它在不同物种和核尺度上的广泛适用性,并提供了有关如何将该平台应用于不同实验系统的信息。

相似文献

1
A versatile image analysis platform for three-dimensional nuclear reconstruction.一种用于三维核重建的多功能图像分析平台。
Methods. 2019 Mar 15;157:15-27. doi: 10.1016/j.ymeth.2018.10.009. Epub 2018 Oct 22.
2
An analytical tool that quantifies cellular morphology changes from three-dimensional fluorescence images.一种可对三维荧光图像中的细胞形态变化进行量化的分析工具。
J Vis Exp. 2012 Aug 31(66):e4233. doi: 10.3791/4233.
3
Deconvolution and chromatic aberration corrections in quantifying colocalization of a transcription factor in three-dimensional cellular space.在三维细胞空间中定量转录因子共定位时的去卷积和色差校正。
Micron. 2010 Aug;41(6):633-40. doi: 10.1016/j.micron.2010.03.005. Epub 2010 Mar 20.
4
Axial tomographic confocal fluorescence microscopy.轴向断层共聚焦荧光显微镜检查。
J Microsc. 2002 Apr;206(Pt 1):7-23. doi: 10.1046/j.1365-2818.2002.01000.x.
5
Analysis of nuclear organization with TANGO, software for high-throughput quantitative analysis of 3D fluorescence microscopy images.使用TANGO对细胞核组织进行分析,TANGO是一款用于三维荧光显微镜图像高通量定量分析的软件。
Methods Mol Biol. 2015;1228:203-22. doi: 10.1007/978-1-4939-1680-1_16.
6
Reconstruction of axial tomographic high resolution data from confocal fluorescence microscopy: a method for improving 3D FISH images.基于共聚焦荧光显微镜的轴向断层高分辨率数据重建:一种改善三维荧光原位杂交图像的方法。
Anal Cell Pathol. 2000;20(1):7-15. doi: 10.1155/2000/459351.
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A robust and versatile platform for image scanning microscopy enabling super-resolution FLIM.用于图像扫描显微镜的强大且多功能平台,可实现超分辨率 FLIM。
Nat Methods. 2019 Feb;16(2):175-178. doi: 10.1038/s41592-018-0291-9. Epub 2019 Jan 14.
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A hybrid blob-slice model for accurate and efficient detection of fluorescence labeled nuclei in 3D.一种混合的斑点-切片模型,用于准确高效地检测 3D 中荧光标记的细胞核。
BMC Bioinformatics. 2010 Nov 29;11:580. doi: 10.1186/1471-2105-11-580.
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Quantitative 3D Analysis of Nuclear Morphology and Heterochromatin Organization from Whole-Mount Plant Tissue Using NucleusJ.使用NucleusJ对整株植物组织的核形态和异染色质组织进行定量三维分析。
Methods Mol Biol. 2018;1675:615-632. doi: 10.1007/978-1-4939-7318-7_33.
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A geometric model for 3-D confocal image analysis.用于三维共聚焦图像分析的几何模型。
IEEE Trans Biomed Eng. 2000 Dec;47(12):1600-9. doi: 10.1109/10.887941.

本文引用的文献

1
Age of heart disease presentation and dysmorphic nuclei in patients with LMNA mutations.LMNA 基因突变患者的心脏疾病发病年龄和核异常。
PLoS One. 2017 Nov 17;12(11):e0188256. doi: 10.1371/journal.pone.0188256. eCollection 2017.
2
Chromatin histone modifications and rigidity affect nuclear morphology independent of lamins.染色质组蛋白修饰和刚性独立于核纤层影响核形态。
Mol Biol Cell. 2018 Jan 15;29(2):220-233. doi: 10.1091/mbc.E17-06-0410. Epub 2017 Nov 15.
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The nucleus: keeping it together by keeping it apart.细胞核:通过分隔来保持完整。
Curr Opin Cell Biol. 2017 Feb;44:44-50. doi: 10.1016/j.ceb.2017.02.001. Epub 2017 Feb 23.
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Mechanosensing by the nucleus: From pathways to scaling relationships.细胞核的机械传感:从信号通路到比例关系
J Cell Biol. 2017 Feb;216(2):305-315. doi: 10.1083/jcb.201610042. Epub 2017 Jan 2.
5
Improved Determination of Subnuclear Position Enabled by Three-Dimensional Membrane Reconstruction.通过三维膜重建实现亚核位置的改进测定
Biophys J. 2016 Jul 12;111(1):19-24. doi: 10.1016/j.bpj.2016.05.036.
6
Causes and consequences of nuclear envelope alterations in tumour progression.肿瘤进展过程中核膜改变的原因及后果
Eur J Cell Biol. 2016 Nov;95(11):449-464. doi: 10.1016/j.ejcb.2016.06.007. Epub 2016 Jun 25.
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Nuclear size is sensitive to NTF2 protein levels in a manner dependent on Ran binding.细胞核大小对NTF2蛋白水平敏感,其方式取决于Ran结合。
J Cell Sci. 2016 Mar 15;129(6):1115-27. doi: 10.1242/jcs.181263. Epub 2016 Jan 28.
8
Nuclear deformability and telomere dynamics are regulated by cell geometric constraints.细胞核的可变形性和端粒动力学受细胞几何约束的调控。
Proc Natl Acad Sci U S A. 2016 Jan 5;113(1):E32-40. doi: 10.1073/pnas.1513189113. Epub 2015 Dec 22.
9
Differential basal-to-apical accessibility of lamin A/C epitopes in the nuclear lamina regulated by changes in cytoskeletal tension.由细胞骨架张力变化调节的核纤层中核纤层蛋白A/C表位从基底到顶端的差异性可及性。
Nat Mater. 2015 Dec;14(12):1252-1261. doi: 10.1038/nmat4389. Epub 2015 Aug 24.
10
Cell shape dependent regulation of nuclear morphology.细胞核形态的细胞形状依赖性调控。
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