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无标记、多参数评估人类和早期鼠类骨关节炎关节软骨细胞代谢和基质重塑。

Label-free, multi-parametric assessments of cell metabolism and matrix remodeling within human and early-stage murine osteoarthritic articular cartilage.

机构信息

Department of Biomedical Engineering, Tufts University, Medford, MA, 02155, USA.

State Key Laboratory of Modern Optical Instrumentation, College of Optical Science and Engineering; International Research Center for Advanced Photonics, Zhejiang University, Hangzhou, Zhejiang, 310027, China.

出版信息

Commun Biol. 2023 Apr 13;6(1):405. doi: 10.1038/s42003-023-04738-w.

Abstract

Osteoarthritis (OA) is characterized by the progressive deterioration of articular cartilage, involving complicated cell-matrix interactions. Systematic investigations of dynamic cellular and matrix changes during OA progression are lacking. In this study, we use label-free two-photon excited fluorescence (TPEF) and second harmonic generation (SHG) imaging to assess cellular and extracellular matrix features of murine articular cartilage during several time points at early stages of OA development following destabilization of medial meniscus surgery. We detect significant changes in the organization of collagen fibers and crosslink-associated fluorescence of the superficial zone as early as one week following surgery. Such changes become significant within the deeper transitional and radial zones at later time-points, highlighting the importance of high spatial resolution. Cellular metabolic changes exhibit a highly dynamic behavior, and indicate metabolic reprogramming from enhanced oxidative phosphorylation to enhanced glycolysis or fatty acid oxidation over the ten-week observation period. The optical metabolic and matrix changes detected within this mouse model are consistent with differences identified in excised human cartilage specimens from OA and healthy cartilage specimens. Thus, our studies reveal important cell-matrix interactions at the onset of OA that may enable improved understanding of OA development and identification of new potential treatment targets.

摘要

骨关节炎(OA)的特征是关节软骨的进行性恶化,涉及复杂的细胞-基质相互作用。缺乏对 OA 进展过程中动态细胞和基质变化的系统研究。在这项研究中,我们使用无标记的双光子激发荧光(TPEF)和二次谐波产生(SHG)成像来评估内侧半月板手术后 OA 早期发展的几个时间点中小鼠关节软骨的细胞和细胞外基质特征。我们早在手术后一周就检测到浅层区胶原纤维组织和交联相关荧光的显著变化。这种变化在稍后的时间点在更深的过渡区和放射区变得显著,突出了高空间分辨率的重要性。细胞代谢变化表现出高度动态的行为,并表明在十周的观察期内,代谢从增强的氧化磷酸化到增强的糖酵解或脂肪酸氧化进行重新编程。在这种小鼠模型中检测到的光学代谢和基质变化与从 OA 患者和健康软骨样本中鉴定出的人软骨样本的差异一致。因此,我们的研究揭示了 OA 发病时重要的细胞-基质相互作用,这可能有助于更好地理解 OA 的发展,并确定新的潜在治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4454/10102009/2d7659ae07a9/42003_2023_4738_Fig1_HTML.jpg

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