[Imaging of bone and joint destruction].

Junichi Kikuta, Masaru Ishii
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引用次数: 0

Abstract

  Osteoclasts are bone-resorbing giant polykaryons that differentiate from mononuclear macrophage/monocyte-lineage hematopoietic precursors. We have originally established an advanced imaging system for visualizing in vivo behavior of osteoclasts and their precursors with intravital two-photon microscopy. By means of the system, we found that sphingosine-1-phosphate, a lipid mediator enriched in blood, controlled the migratory behavior of osteoclast precursors. We also developed pH-sensing chemical fluorescent probes to detect localized acidification by bone-resorbing osteoclasts on the bone surface in vivo, and identified two distinct functional states of differentiated osteoclasts, 'bone-resorptive' and 'non-resorptive'. In this review, we summarize our recent studies on the dynamics and functions of osteoclasts. Our intravital imaging techniques would be beneficial for studying the cellular dynamics in arthritic inflammation and bone destruction in vivo and would thus be useful for evaluating novel therapies targeting aspects of osteoclast dynamics in patients with bone-destructive diseases.

[骨骼和关节破坏的成像]。
破骨细胞是吸收骨的巨大多核细胞,与单核巨噬细胞/单核细胞系造血前体分化。我们最初建立了一个先进的成像系统,用于活体双光子显微镜观察破骨细胞及其前体的体内行为。通过该系统,我们发现血液中富集的脂质介质鞘氨醇-1-磷酸控制破骨细胞前体的迁移行为。我们还开发了ph感应化学荧光探针,用于检测体内骨表面由骨吸收破骨细胞引起的局部酸化,并鉴定了分化破骨细胞的两种不同功能状态,“骨吸收”和“非吸收”。本文就近年来在破骨细胞动力学和功能方面的研究进展作一综述。我们的活体成像技术将有助于研究体内关节炎炎症和骨破坏的细胞动力学,从而有助于评估针对骨破坏疾病患者破骨细胞动力学方面的新疗法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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