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光学相干断层扫描用于在体成像小鼠发育的高分辨率图像。

Optical coherence tomography for high-resolution imaging of mouse development in utero.

机构信息

Department of Biomedical Engineering, University of Houston, 4800 Calhoun Road, 3605 Cullen Boulevard, Houston, Texas 77204, USA.

出版信息

J Biomed Opt. 2011 Apr;16(4):046004. doi: 10.1117/1.3560300.

DOI:10.1117/1.3560300
PMID:21529073
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3081861/
Abstract

Although the mouse is a superior model to study mammalian embryonic development, high-resolution live dynamic visualization of mouse embryos remain a technical challenge. We present optical coherence tomography as a novel methodology for live imaging of mouse embryos through the uterine wall thereby allowing for time lapse analysis of developmental processes and direct phenotypic analysis of developing embryos. We assessed the capability of the proposed methodology to visualize structures of the living embryo from embryonic stages 12.5 to 18.5 days postcoitus. Repetitive in utero embryonic imaging is demonstrated. Our work opens the door for a wide range of live, in utero embryonic studies to screen for mutations and understand the effects of pharmacological and toxicological agents leading to birth defects.

摘要

虽然老鼠是研究哺乳动物胚胎发育的优秀模型,但要对老鼠胚胎进行高分辨率的实时动态可视化仍然是一项技术挑战。我们提出了光学相干断层扫描作为一种新的方法,通过子宫壁对老鼠胚胎进行实时成像,从而可以对发育过程进行延时分析,并直接对发育中的胚胎进行表型分析。我们评估了该方法从受孕后 12.5 天到 18.5 天的胚胎阶段对活体胚胎结构进行可视化的能力。重复性的宫内胚胎成像得到了验证。我们的工作为广泛的活体宫内胚胎研究开辟了道路,可以筛选突变并了解导致出生缺陷的药理学和毒理学因素的影响。

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本文引用的文献

1
Imaging modalities to assess structural birth defects in mutant mouse models.用于评估突变小鼠模型中结构出生缺陷的成像方式。
Birth Defects Res C Embryo Today. 2010 Sep;90(3):176-84. doi: 10.1002/bdrc.20187.
2
Live Imaging of Early Developmental Processes in Mammalian Embryos with Optical Coherence Tomography.利用光学相干断层扫描对哺乳动物胚胎早期发育过程进行活体成像。
J Innov Opt Health Sci. 2009 Jan 1;2(3):253-259. doi: 10.1142/S1793545809000619.
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Mouse phenogenomics, toolbox for functional annotation of human genome.鼠类基因功能基因组学——人类基因组功能注释的工具盒。
BMB Rep. 2010 Feb;43(2):79-90. doi: 10.5483/bmbrep.2010.43.2.079.
4
EuroPhenome: a repository for high-throughput mouse phenotyping data.欧洲表型组学数据库:一个用于高通量小鼠表型数据的存储库。
Nucleic Acids Res. 2010 Jan;38(Database issue):D577-85. doi: 10.1093/nar/gkp1007. Epub 2009 Nov 23.
5
Use of KikGR a photoconvertible green-to-red fluorescent protein for cell labeling and lineage analysis in ES cells and mouse embryos.使用KikGR(一种光转化型绿色至红色荧光蛋白)对胚胎干细胞和小鼠胚胎进行细胞标记和谱系分析。
BMC Dev Biol. 2009 Sep 9;9:49. doi: 10.1186/1471-213X-9-49.
6
The functional annotation of mammalian genomes: the challenge of phenotyping.哺乳动物基因组的功能注释:表型分析的挑战。
Annu Rev Genet. 2009;43:305-33. doi: 10.1146/annurev-genet-102108-134143.
7
Hemodynamic measurements from individual blood cells in early mammalian embryos with Doppler swept source OCT.利用多普勒扫频源光学相干断层扫描技术测量早期哺乳动物胚胎中单个血细胞的血流动力学参数。
Opt Lett. 2009 Apr 1;34(7):986-8. doi: 10.1364/ol.34.000986.
8
In vivo virtual histology of mouse embryogenesis by ultrasound biomicroscopy and magnetic resonance imaging.通过超声生物显微镜和磁共振成像对小鼠胚胎发育进行体内虚拟组织学研究。
Reprod Fertil Dev. 2009;21(2):283-92. doi: 10.1071/rd08124.
9
Live imaging of blood flow in mammalian embryos using Doppler swept-source optical coherence tomography.使用多普勒扫频源光学相干断层扫描对哺乳动物胚胎中的血流进行实时成像。
J Biomed Opt. 2008 Nov-Dec;13(6):060506. doi: 10.1117/1.3046716.
10
Vascular remodeling of the mouse yolk sac requires hemodynamic force.小鼠卵黄囊的血管重塑需要血流动力学力。
Development. 2007 Sep;134(18):3317-26. doi: 10.1242/dev.02883.