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本文引用的文献

1
Knockdown of the pericellular matrix molecule perlecan lowers in situ cell and matrix stiffness in developing cartilage.敲低细胞周围基质分子基底膜聚糖会降低发育中软骨的原位细胞和基质硬度。
Dev Biol. 2016 Oct 15;418(2):242-7. doi: 10.1016/j.ydbio.2016.08.029. Epub 2016 Aug 27.
2
Nanoindentation modulus of murine cartilage: a sensitive indicator of the initiation and progression of post-traumatic osteoarthritis.小鼠软骨的纳米压痕模量:创伤后骨关节炎发生和进展的敏感指标。
Osteoarthritis Cartilage. 2017 Jan;25(1):108-117. doi: 10.1016/j.joca.2016.08.008. Epub 2016 Aug 25.
3
Nanomechanics of Engineered Articular Cartilage: Synergistic Influences of Transforming Growth Factor-β3 and Oscillating Pressure.工程化关节软骨的纳米力学:转化生长因子-β3与振荡压力的协同影响
J Nanosci Nanotechnol. 2016 Mar;16(3):3136-3145. doi: 10.1166/jnn.2016.12564.
4
In vivo Sarcomere Lengths and Sarcomere Elongations Are Not Uniform across an Intact Muscle.在完整肌肉中,肌节长度和肌节伸长在体内并非均匀一致。
Front Physiol. 2016 May 25;7:187. doi: 10.3389/fphys.2016.00187. eCollection 2016.
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High-Throughput Assessment of Cellular Mechanical Properties.细胞力学特性的高通量评估
Annu Rev Biomed Eng. 2015;17:35-62. doi: 10.1146/annurev-bioeng-071114-040545. Epub 2015 Jul 16.
6
High-bandwidth AFM-based rheology is a sensitive indicator of early cartilage aggrecan degradation relevant to mouse models of osteoarthritis.基于高带宽原子力显微镜的流变学是与骨关节炎小鼠模型相关的早期软骨聚集蛋白聚糖降解的敏感指标。
J Biomech. 2015 Jan 2;48(1):162-5. doi: 10.1016/j.jbiomech.2014.11.012. Epub 2014 Nov 18.
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Effects of cryopreservation on the depth-dependent elastic modulus in articular cartilage and implications for osteochondral grafting.冷冻保存对关节软骨深度依赖性弹性模量的影响及其对骨软骨移植的意义。
J Biomech Eng. 2015 May;137(5):054502. doi: 10.1115/1.4029182. Epub 2015 Mar 6.
8
Quantitative proteomics at different depths in human articular cartilage reveals unique patterns of protein distribution.对人关节软骨不同深度进行的定量蛋白质组学研究揭示了独特的蛋白质分布模式。
Matrix Biol. 2014 Nov;40:34-45. doi: 10.1016/j.matbio.2014.08.013. Epub 2014 Sep 1.
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How best to preserve and reveal the structural intricacies of cartilaginous tissue.如何最好地保存和揭示软骨组织的结构复杂性。
Matrix Biol. 2014 Oct;39:33-43. doi: 10.1016/j.matbio.2014.08.010. Epub 2014 Aug 27.
10
Proteoglycan concentrations in healthy and diseased articular cartilage by Fourier transform infrared imaging and principal component regression.通过傅里叶变换红外成像和主成分回归分析健康及病变关节软骨中的蛋白聚糖浓度
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利用光学成像至扫描探针显微镜研究软骨细胞和关节软骨的功能特性。

Functional properties of chondrocytes and articular cartilage using optical imaging to scanning probe microscopy.

作者信息

Xia Yang, Darling Eric M, Herzog Walter

机构信息

Department of Physics and Center for Biomedical Research, Oakland University, Rochester, Michigan, 48309.

Department of Molecular Pharmacology, Physiology, and Biotechnology, School of Engineering, Dept of Orthopaedics, Center for Biomedical Engineering, Brown University, Providence, Rhode Island, 02912.

出版信息

J Orthop Res. 2018 Feb;36(2):620-631. doi: 10.1002/jor.23757. Epub 2017 Nov 22.

DOI:10.1002/jor.23757
PMID:28975657
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5839958/
Abstract

Mature chondrocytes in adult articular cartilage vary in number, size, and shape, depending on their depth in the tissue, location in the joint, and source species. Chondrocytes are the primary structural, functional, and metabolic unit in articular cartilage, the loss of which will induce fatigue to the extracellular matrix (ECM), eventually leading to failure of the cartilage and impairment of the joint as a whole. This brief review focuses on the functional and biomechanical studies of chondrocytes and articular cartilage, using microscopic imaging from optical microscopies to scanning probe microscopy. Three topics are covered in this review, including the functional studies of chondrons by optical imaging (unpolarized and polarized light and infrared light, two-photon excitation microscopy), the probing of chondrocytes and cartilage directly using microscale measurement techniques, and different imaging approaches that can measure chondrocyte mechanics and chondrocyte biological signaling under in situ and in vivo environments. Technical advancement in chondrocyte research during recent years has enabled new ways to study the biomechanical and functional properties of these cells and cartilage. © 2017 Orthopaedic Research Society. Published by Wiley Periodicals, Inc. J Orthop Res 36:620-631, 2018.

摘要

成年关节软骨中的成熟软骨细胞在数量、大小和形状上存在差异,这取决于它们在组织中的深度、在关节中的位置以及来源物种。软骨细胞是关节软骨中的主要结构、功能和代谢单位,其缺失会导致细胞外基质(ECM)疲劳,最终导致软骨失效和整个关节受损。本简要综述聚焦于软骨细胞和关节软骨的功能及生物力学研究,采用从光学显微镜到扫描探针显微镜的微观成像技术。本综述涵盖三个主题,包括通过光学成像(非偏振光和偏振光以及红外光、双光子激发显微镜)对软骨粒进行功能研究、直接使用微观测量技术探测软骨细胞和软骨,以及能够在原位和体内环境下测量软骨细胞力学和软骨细胞生物信号的不同成像方法。近年来软骨细胞研究的技术进步为研究这些细胞和软骨的生物力学及功能特性提供了新途径。© 2017骨科研究协会。由威利期刊公司出版。《矫形外科学研究》36:620 - 631,2018年。