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Characterization of the Developing Lacunocanalicular Network During Fracture Repair

机译:骨折修复过程中发育中的颅小管网络的特征

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摘要

Fracture repair is a normal physiological response to bone injury. During the process of bony callus formation, a lacunocanalicular network (LCN) is formed de novo that evolves with callus remodeling. Our aim was the longitudinal assessment of the development and evolution of the LCN during fracture repair. To this end, 45 adult wild‐type C57BL/6 mice underwent closed tibial fracture surgery. Fractured and intact contralateral tibias were harvested after 2, 3, and 6 weeks of bone healing (n = 15/group). High‐resolution micro–computed tomography (μCT) and deconvolution microscopy (DV) approaches were applied to quantify lacunar number density from the calluses and intact bone. On histological sections, Goldner's trichrome staining was used to assess lacunar occupancy, fluorescein isothiocyanate staining to visualize the canalicular network, and terminal deoxynucleotidyl transferase–mediated deoxyuridine triphosphate‐biotin nick end labeling (TUNEL) staining to examine osteocyte apoptosis. Analysis of μCT scans showed progressive decreases in mean lacuna volume over time (−27% 2–3 weeks; −13% 3–6 weeks). Lacunar number density increased considerably between 2 and 3 weeks (+156%). Correlation analysis was performed, showing a positive linear relationship between canalicular number density and trabecular thickness (R 2 = 0.56, p 90%), but the old cortical bone within the fracture site appeared necrotic as it underwent resorption. In conclusion, our data shows a progressive increase in the complexity of the LCN over time during fracture healing and demonstrates that this network is initiated during the early stages of repair. Further studies are needed to address the functional importance of osteocytes in bone healing, particularly in detecting and translating the effects of micromotion in the fracture. © 2021 The Authors. JBMR Plus published by Wiley Periodicals LLC on behalf of American Society for Bone and Mineral Research.
机译:骨折修复是对骨损伤的正常生理反应。在骨性愈伤组织形成过程中,腔隙小核网络 (LCN) 会随着愈伤组织重塑而从头形成。我们的目标是纵向评估骨折修复过程中 LCN 的发展和演变。为此,45 只成年野生型 C57BL/6 小鼠接受了闭合性胫骨骨折手术。骨折和完整的对侧胫骨在骨愈合 2 、 3 和 6 周后收获 (n = 15/组)。采用高分辨率显微计算机断层扫描 (μCT) 和反卷积显微镜 (DV) 方法来量化来自愈伤组织和完整骨骼的腔隙数密度。在组织学切片上,Goldner 三色染色用于评估腔隙占有率,异硫氰酸荧光素染色以可视化小管网络,末端脱氧核苷酸转移酶介导的脱氧尿嘧啶三磷酸-生物素缺口末端标记 (TUNEL) 染色以检查骨细胞凋亡。μCT 扫描分析显示,平均腔隙体积随着时间的推移逐渐减少(2-3 周为 -27%;3-6 周为 -13%)。腔隙数密度在 2 至 3 周之间显著增加 (+156%)。进行相关性分析,显示小管数密度与小梁厚度呈正线性关系 (R 2 = 0.56,p 90%),但骨折部位的旧皮质骨在吸收过程中出现坏死。总之,我们的数据显示,在骨折愈合过程中,LCN 的复杂性随着时间的推移而逐渐增加,并表明该网络是在修复的早期阶段启动的。需要进一步的研究来解决骨细胞在骨愈合中的功能重要性,特别是在检测和转化微动对骨折的影响方面。© 2021 作者。JBMR Plus 由 Wiley Periodicals LLC 代表美国骨骼和矿物研究协会出版。

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