三维反褶积明场显微镜的亚细胞显微解剖:间期细胞核中人类染色质的方法和分析。

Anatomy research international Pub Date : 2012-01-01 Epub Date: 2012-01-24 DOI:10.1155/2012/848707
Paul Joseph Tadrous
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引用次数: 3

摘要

解剖学在宏观(例如,解剖,血管注射成型,放射学)和微观(例如,用光学和电子显微镜进行连续切片重建)水平上使用三维(3D)研究取得了进展。本文介绍了一种新的亚细胞三维明场显微技术在人体细胞中的首次应用结果。与传统的三维反卷积和共聚焦技术不同,该方法适用于明场显微镜的一般应用。与明场连续切片不同,它具有亚细胞分辨率。本文报道了两种人类细胞(肝细胞和浆细胞)间期细胞核染色质的三维结构。我展示了如何在3D中自由地检查这些结构,允许细胞类型之间和细胞类型内部更大的形态区分,并揭示了浆细胞核经典“钟面”基序的3D结构基础。讨论了进一步应用的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Subcellular Microanatomy by 3D Deconvolution Brightfield Microscopy: Method and Analysis Using Human Chromatin in the Interphase Nucleus.

Subcellular Microanatomy by 3D Deconvolution Brightfield Microscopy: Method and Analysis Using Human Chromatin in the Interphase Nucleus.

Subcellular Microanatomy by 3D Deconvolution Brightfield Microscopy: Method and Analysis Using Human Chromatin in the Interphase Nucleus.

Subcellular Microanatomy by 3D Deconvolution Brightfield Microscopy: Method and Analysis Using Human Chromatin in the Interphase Nucleus.

Anatomy has advanced using 3-dimensional (3D) studies at macroscopic (e.g., dissection, injection moulding of vessels, radiology) and microscopic (e.g., serial section reconstruction with light and electron microscopy) levels. This paper presents the first results in human cells of a new method of subcellular 3D brightfield microscopy. Unlike traditional 3D deconvolution and confocal techniques, this method is suitable for general application to brightfield microscopy. Unlike brightfield serial sectioning it has subcellular resolution. Results are presented of the 3D structure of chromatin in the interphase nucleus of two human cell types, hepatocyte and plasma cell. I show how the freedom to examine these structures in 3D allows greater morphological discrimination between and within cell types and the 3D structural basis for the classical "clock-face" motif of the plasma cell nucleus is revealed. Potential for further applications discussed.

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