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使用量子点605对未处理和7-酮胆固醇处理的人单核细胞进行CD36表达的流式细胞术和光谱成像多光子显微镜分析。

Flow cytometry and spectral imaging multiphoton microscopy analysis of CD36 expression with quantum dots 605 of untreated and 7-ketocholesterol-treated human monocytic cells.

作者信息

Kahn Edmond, Ménétrier Franck, Vejux Anne, Montange Thomas, Dumas Dominique, Riedinger Jean-Marc, Frouin Frédérique, Tourneur Yves, Brau Frédéric, Stoltz Jean-François, Lizard Gérard

机构信息

National Institute of Health and Medical Research, U678/Mixed Research Unit S UPMC, Paris, France.

出版信息

Anal Quant Cytol Histol. 2006 Dec;28(6):316-30.

Abstract

OBJECTIVE

To evaluate CD36 expression with quantum dots 605 (QDs 605) on untreated and 7-ketocholesterol (7KC)-treated monocytic U937 cells by flow cytometry (FCM) and confocal and multiphoton laser scanning microscopy (CLSM).

STUDY DESIGN

Cells were analyzed by CLSM, following flow cytometric quantification of CD36 expression and 7KC uptake. Image sequences were obtained by spectral analysis in monophoton and multiphoton CLSM and analyzed by the factor analysis of medical image sequences (FAMIS) algorithm to differentiate emission spectra. In CLSM analysis, cell deposits were screened in ultraviolet excitation modes to optimize the possibilities of QDs 605 and have the benefit of nuclei counterstaining by DAPI.

RESULTS

FCM and CLSM reveal the expression of CD36 by means of QDs 605. FCM provides information on 7KC uptake. CLSM provides the localization of 7KC vs. DAPI. As factor curves and images show the red, narrow emission of QDs 605 vs. violet and blue emissions of 7KC and DAPI, respectively, a reliable identification of CD36 is obtained.

CONCLUSION

QDs 605 are useful tools to perform antigenic expression in FCM and CLSM. Moreover, CLSM and subsequent spectral analysis provide a more specific characterization of QDs 605 fluorescent emission in the UV excitation mode and a simultaneous identification of 7KC.

摘要

目的

通过流式细胞术(FCM)、共聚焦和多光子激光扫描显微镜(CLSM),利用量子点605(QDs 605)评估未处理及经7-酮胆固醇(7KC)处理的单核细胞U937细胞中CD36的表达。

研究设计

在对CD36表达和7KC摄取进行流式细胞术定量后,通过CLSM对细胞进行分析。通过单光子和多光子CLSM中的光谱分析获得图像序列,并采用医学图像序列因子分析(FAMIS)算法进行分析以区分发射光谱。在CLSM分析中,在紫外激发模式下筛选细胞沉积物,以优化QDs 605的应用可能性,并受益于用DAPI对细胞核进行复染。

结果

FCM和CLSM通过QDs 605揭示了CD36的表达。FCM提供了关于7KC摄取的信息。CLSM提供了7KC与DAPI的定位。由于因子曲线和图像分别显示了QDs 605的红色窄发射与7KC和DAPI的紫色和蓝色发射,因此可可靠地鉴定CD36。

结论

QDs 605是在FCM和CLSM中进行抗原表达的有用工具。此外,CLSM及后续光谱分析在紫外激发模式下对QDs 605荧光发射提供了更具体的表征,并能同时鉴定7KC。

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