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原子力显微镜作为分析工具研究肠道细胞的物理机械性能。

Atomic force microscopy as analytical tool to study physico-mechanical properties of intestinal cells.

机构信息

Institute of Pharmaceutical Sciences, Department of Pharmaceutical Technology, NAWI Graz, Karl-Franzens-University of Graz, BioTechMed-Graz, Austria.

Medical University of Graz, Center for Medical Research, BioTechMed-Graz, Austria.

出版信息

Beilstein J Nanotechnol. 2015 Jul 6;6:1457-66. doi: 10.3762/bjnano.6.151. eCollection 2015.

Abstract

The small intestine is a complex system that carries out various functions. The main function of enterocytes is absorption of nutrients, whereas membranous cells (M cells) are responsible for delivering antigens/foreign substances to the mucosal lymphoid tissues. However, to get a fundamental understanding of how cellular structures contribute to physiological processes, precise knowledge about surface morphologies, cytoskeleton organizations and biomechanical properties is necessary. Atomic force microscopy (AFM) was used here as a powerful tool to study surface topographies of Caco-2 cells and M cells. Furthermore, cell elasticity (i.e., the mechanical response of a cell on a tip indentation), was elucidated by force curve measurements. Besides elasticity, adhesion was evaluated by recording the attraction and repulsion forces between the tip and the cell surface. Organization of F-actin networks were investigated via phalloidin labeling and visualization was performed with confocal laser scanning fluorescence microscopy (CLSM) and scanning electron microscopy (SEM). The results of these various experimental techniques revealed significant differences in the cytoskeleton/microvilli arrangements and F-actin organization. Caco-2 cells displayed densely packed F-actin bundles covering the entire cell surface, indicating the formation of a well-differentiated brush border. In contrast, in M cells actins were arranged as short and/or truncated thin villi, only available at the cell edge. The elasticity of M cells was 1.7-fold higher compared to Caco-2 cells and increased significantly from the cell periphery to the nuclear region. Since elasticity can be directly linked to cell adhesion, M cells showed higher adhesion forces than Caco-2 cells. The combination of distinct experimental techniques shows that morphological differences between Caco-2 cells and M cells correlate with mechanical cell properties and provide useful information to understand physiological processes/mechanisms in the small intestine.

摘要

小肠是一个复杂的系统,执行各种功能。肠细胞的主要功能是吸收营养物质,而膜细胞(M 细胞)则负责将抗原/外来物质递送到黏膜淋巴组织。然而,要深入了解细胞结构如何促进生理过程,就需要精确了解表面形态、细胞骨架组织和生物力学特性。原子力显微镜(AFM)在这里被用作研究 Caco-2 细胞和 M 细胞表面形貌的有力工具。此外,通过力曲线测量阐明了细胞弹性(即细胞对尖端压痕的机械响应)。除了弹性之外,还通过记录尖端和细胞表面之间的吸引力和排斥力来评估粘附力。通过鬼笔环肽标记研究 F-肌动蛋白网络的组织,并通过共聚焦激光扫描荧光显微镜(CLSM)和扫描电子显微镜(SEM)进行可视化。这些各种实验技术的结果显示出细胞骨架/微绒毛排列和 F-肌动蛋白组织的显著差异。Caco-2 细胞显示出密集排列的 F-肌动蛋白束覆盖整个细胞表面,表明形成了良好分化的刷状缘。相比之下,M 细胞中的肌动蛋白排列为短而/或截断的薄微绒毛,仅存在于细胞边缘。与 Caco-2 细胞相比,M 细胞的弹性高 1.7 倍,并且从细胞边缘到核区域显著增加。由于弹性可以直接与细胞粘附相关联,因此 M 细胞显示出比 Caco-2 细胞更高的粘附力。不同实验技术的组合表明,Caco-2 细胞和 M 细胞之间的形态差异与机械细胞特性相关,并为理解小肠中的生理过程/机制提供了有用的信息。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8604/4505173/4d00409a0385/Beilstein_J_Nanotechnol-06-1457-g002.jpg

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