首页> 美国卫生研究院文献>Journal of Assisted Reproduction and Genetics >Spectral Imaging in Preconception/Preimplantation Genetic Diagnosis of Aneuploidy: Multicolor Multichromosome Screening of Single Cells
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Spectral Imaging in Preconception/Preimplantation Genetic Diagnosis of Aneuploidy: Multicolor Multichromosome Screening of Single Cells

机译:非整倍体的孕前/着床前遗传学诊断中的光谱成像:单细胞的多色多染色体筛选

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摘要

>Purpose:Our purpose was to evaluate the utility of spectral imaging for multicolor, multichromosome enumeration in human interphase cell nuclei.>Methods:Chromosome-specific probes labeled with different fluorochromes or nonfluorescent haptens were obtained commercially or prepared in-house. Metaphase spreads, interphase lymphocytes, or blastomeres cells were hybridized with either 7 or 11 distinctly different probes. Following 46 hr of hybridization, slides were washed and detected using either a filter-based quantitative image processing system (QUIPS) developed in-house or a commercial spectral imaging system.>Results:The filter-based fluorescence microscope system is preferred for simultaneous detection of up to seven chromosome targets because of its high sensitivity and speed. However, this approach may not be applicable to interphase cells when 11 or more targets need to be discriminated. Interferometer-based spectral imaging with a spectral resolution of approximately 10 nm allows labeling of chromosome-specific DNA probes with fluorochromes having greatly overlapping emission spectra. This leads to increases in the number of fluorochromes or fluorochrome combinations available to score unambiguously chromosomes in interphase nuclei.>Conclusions:Spectral imaging provides a significant improvement over conventional filter-based microscope systems for enumeration of multiple chromosomes in interphase nuclei, although further technical development is necessary in its application to embryonic blastomeres. When applied to preconception/preimplantation genetic diagnosis, presently available probes for spectral imaging are expected to detect abnormalities responsible for 70–80% of spontaneous abortions caused by chromosomal trisomies.
机译:>目的:我们的目的是评估光谱成像在人间期细胞核中进行多色,多染色体计数的实用性。>方法:标记有不同荧光染料或非荧光半抗原的染色体特异性探针可以通过商业途径获得或自行制备。中期扩散,间期淋巴细胞或卵裂球细胞与7或11种明显不同的探针杂交。杂交46小时后,用内部开发的基于过滤器的定量图像处理系统(QUIPS)或商用光谱成像系统洗涤并检测载玻片。>结果:基于过滤器的荧光显微镜该系统可同时检测多达七个染色体靶标,因为它具有很高的灵敏度和速度,因此是首选。但是,当需要区分11个或更多目标时,此方法可能不适用于相间单元。基于干涉仪的光谱成像具有约10 nm的光谱分辨率,可以用发射光谱大大重叠的荧光染料标记染色体特异性DNA探针。这导致可用于对相间核中的染色体进行明确评分的荧光染料或荧光染料组合的数量增加。>结论:与常规基于过滤器的显微镜系统(用于枚举相间多个染色体)相比,光谱成像显着改进核,尽管将其应用于胚胎卵裂球需要进一步的技术发展。当应用于孕前/植入前的遗传学诊断时,目前可用的光谱成像探针有望检测到由染色体三体性疾病引起的自然流产的70-80%。

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