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Atomic force microscopy imaging and 3-D reconstructions of serial thin sections of a single cell and its interior structures

机译:原子力显微镜成像和单个细胞及其内部结构的连续薄片的3-D重建

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The thin sectioning has been widely applied in electron microscopy (EM), and successfully used for an in situ observation of inner ultrastructure of cells. This powerful technique has recently been extended to the research field of atomic force microscopy (AFM). However, there have been no reports describing AFM imaging of serial thin sections and three-dimensional (3-D) reconstruction of cells and their inner structures. In the present study, we used AFM to scan serial thin sections approximately 60 rim thick of a mouse embryonic stem (ES) cell, and to observe the in situ inner ultrastructure including cell membrane, cytoplasm, mitochondria, nucleus membrane, and linear chromatin. The high-magnification AFM imaging of single mitochondria clearly demonstrated the outer membrane, inner boundary membrane and cristal membrane of mitochondria in the cellular compartment. Importantly, AFM imaging on six serial thin sections of a single mouse ES cell showed that mitochondria underwent sequential changes in the number, morphology and distribution. These nanoscale images allowed us to perform 3-D surface reconstruction of interested interior structures in cells. Based on the serial in situ images, 3-D models of morphological characteristics, numbers and distributions of interior structures of the single ES cells were validated and reconstructed. Our results suggest that the combined AFM and serial-thin-section technique is useful for the nanoscale imaging and 3-D reconstruction of single cells and their inner structures. This technique may facilitate studies of proliferating and differentiating stages of stem cells or somatic cells at a nanoscale.
机译:薄切片已广泛应用于电子显微镜(EM),并成功用于原位观察细胞的内部超微结构。这项强大的技术最近已扩展到原子力显微镜(AFM)的研究领域。但是,还没有报道描述连续薄切片的AFM成像以及细胞及其内部结构的三维(3-D)重建。在本研究中,我们使用原子力显微镜(AFM)扫描小鼠胚胎干(ES)细胞约60 rim厚的连续薄片,并观察原位内部超微结构,包括细胞膜,细胞质,线粒体,核膜和线性染色质。单线粒体的高倍率原子力显微镜成像清楚地显示了细胞室内线粒体的外膜,内边界膜和晶体膜。重要的是,在单个小鼠ES细胞的六个连续薄切片上进行的AFM成像显示,线粒体的数量,形态和分布发生了连续变化。这些纳米级图像使我们能够对细胞中感兴趣的内部结构进行3-D表面重建。基于串行原位图像,验证并重建了3D模型的单个ES细胞的形态特征,数量和内部结构分布。我们的结果表明,AFM和连续薄截面技术相结合可用于纳米成像和单细胞及其内部结构的3-D重建。该技术可以促进纳米级干细胞或体细胞增殖和分化阶段的研究。

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