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1
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2
LeftyA decreases Actin Polymerization and Stiffness in Human Endometrial Cancer Cells.LeftyA 降低人子宫内膜癌细胞中的肌动蛋白聚合和刚性。
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Stiffness of Intact Endothelial Cells From Fresh Aortic Bifurcations of Atherosclerotic Rabbits-Atomic Force Microscopic Study.动脉粥样硬化兔新鲜主动脉分叉处完整内皮细胞刚性的原子力显微镜研究。
J Cell Physiol. 2017 Jan;232(1):7-13. doi: 10.1002/jcp.25379. Epub 2016 Aug 10.
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Efficient extravasation of tumor-repopulating cells depends on cell deformability.肿瘤再增殖细胞的有效外渗取决于细胞的可变形性。
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Localized cell stiffness measurement using axial movement of an optically trapped microparticle.使用光阱微粒子的轴向运动进行局部细胞硬度测量。
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Measuring the mechanical properties of living cells using atomic force microscopy.使用原子力显微镜测量活细胞的力学特性。
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细胞胆固醇调节单核细胞变形。

Cellular cholesterol regulates monocyte deformation.

作者信息

Saha Amit K, Dallo Shatha F, Detmar Ariana L, Osmulski Pawel, Gaczynska Maria, Huang Tim Hui-Ming, Ramasubramanian Anand K

机构信息

Department of Biomedical Engineering, The University of Texas at San Antonio, San Antonio, TX, United States.

Department of Molecular Medicine, The University of Texas Health Science Center at San Antonio, San Antonio, TX, United States.

出版信息

J Biomech. 2017 Feb 8;52:83-88. doi: 10.1016/j.jbiomech.2016.12.033. Epub 2016 Dec 30.

DOI:10.1016/j.jbiomech.2016.12.033
PMID:28082022
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5736503/
Abstract

The role of cholesterol content on monocyte biomechanics remains understudied despite the well-established link between cholesterol and monocytes/macrophages in atherosclerosis, and the effect on other cell types. In this work, we have investigated the effect of cholesterol on monocyte deformability and the underlying molecular mechanisms. We altered the baseline cholesterol in human monocytic cell line THP-1, and investigated the changes in monocyte deformability using a custom microfluidic platform and atomic force microscopy. We observed that the cholesterol depletion lowered deformability while enrichment increased deformability compared to untreated cells. As a consequence of altered deformability, cholesterol depleted cells spread more on collagen-coated surfaces with elongated morphology, whereas cholesterol enriched cells had a more rounded morphology. We observed that the decreased deformability in cholesterol depleted cells, despite an increase in the fluidity of the membrane, is due to an increase in phosphorylation of Protein Kinase C (PKC), which translates to a higher degree of actin polymerization. Together, our results highlight the importance of biophysical regulation of monocyte response to cholesterol levels.

摘要

尽管胆固醇与动脉粥样硬化中的单核细胞/巨噬细胞之间已确立联系,且对其他细胞类型也有影响,但胆固醇含量对单核细胞生物力学的作用仍未得到充分研究。在这项工作中,我们研究了胆固醇对单核细胞变形能力及其潜在分子机制的影响。我们改变了人类单核细胞系THP-1中的基线胆固醇水平,并使用定制的微流控平台和原子力显微镜研究了单核细胞变形能力的变化。我们观察到,与未处理的细胞相比,胆固醇耗竭降低了变形能力,而胆固醇富集则增加了变形能力。由于变形能力的改变,胆固醇耗竭的细胞在胶原包被的表面上更易铺展,形态呈细长状,而胆固醇富集的细胞形态更圆。我们观察到,胆固醇耗竭的细胞中变形能力下降,尽管膜的流动性增加,这是由于蛋白激酶C(PKC)磷酸化增加所致,这导致肌动蛋白聚合程度更高。总之,我们的结果突出了对单核细胞对胆固醇水平反应进行生物物理调节的重要性。