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雌激素缺乏相关的腔隙周围吸收和骨细胞凋亡过程中皮质微孔隙度的时间变化:一项初步研究。

Temporal changes in cortical microporosity during estrogen deficiency associated with perilacunar resorption and osteocyte apoptosis: A pilot study.

作者信息

Allison H, O'Sullivan L M, McNamara L M

机构信息

Mechanobiology and Medical Devices Research Group (MMDRG), Centre for Biomechanics Research (BioMEC), Biomedical Engineering, College of Science and Engineering, National University of Ireland Galway, Ireland.

出版信息

Bone Rep. 2022 May 17;16:101590. doi: 10.1016/j.bonr.2022.101590. eCollection 2022 Jun.

Abstract

Osteocytes can actively regulate bone microporosity, through either perilacunar resorption or micropetrosis following apoptosis. Osteocyte apoptosis is more prevalent in estrogen deficiency and changes in the lacunar-canalicular network of osteocytes have been reported. Temporal changes in bone mineralisation and osteocytes cellular strains occur, which might be associated with osteocyte-driven microporosity changes, although time dependant changes in bone microporosity are not yet fully understood. In this pilot study we conducted micro-CT analysis, backscatter electron imaging and histological analysis of femoral cortical bone form an ovariectomized rat model of osteoporosis to investigate whether estrogen deficiency causes temporal changes in lacunar and vascular porosity. We also assessed MMP14 expression, lacunar occupancy and mineral infilling, as indicators of perilacunar resorption and micropetrosis. We report temporal changes in cortical microporosity in estrogen deficiency. Specifically, canalicular and vascular porosity initially increased (4 weeks post-OVX), coinciding with the period of rapid bone loss, whereas in the longer term (14 weeks post-OVX) lacunar and canalicular diameter decreased. Interestingly, these changes coincided with an increased prevalence of empty lacunae and osteocyte lacunae were observed to be more circular with a mineralised border around the lacunar space. In addition we report an increase in MMP14+ osteocytes, which also suggests active matrix degradation by these cells. Together these results provide an insight into the temporal changes in cortical microporosity during estrogen deficiency and suggest the likelihood of occurrence of both perilacunar resorption and osteocyte apoptosis leading to micropetrosis. We propose that microporosity changes arise due to processes driven by distinct populations of osteocytes, which are either actively resorbing their matrix or have undergone apoptosis and are infilling lacunae by micropetrosis.

摘要

骨细胞可通过凋亡后陷窝周围吸收或微石化作用来积极调节骨微孔隙率。骨细胞凋亡在雌激素缺乏时更为普遍,并且已有报道称骨细胞的腔隙-小管网络发生了变化。骨矿化和骨细胞细胞应变存在时间性变化,这可能与骨细胞驱动的微孔隙率变化有关,尽管骨微孔隙率的时间依赖性变化尚未完全了解。在这项初步研究中,我们对去卵巢骨质疏松大鼠模型的股骨皮质骨进行了显微CT分析、背散射电子成像和组织学分析,以研究雌激素缺乏是否会导致腔隙和血管孔隙率的时间性变化。我们还评估了MMP14表达、腔隙占有率和矿物质填充情况,作为陷窝周围吸收和微石化作用的指标。我们报告了雌激素缺乏时皮质微孔隙率的时间性变化。具体而言,小管和血管孔隙率最初增加(去卵巢后4周),与快速骨丢失期一致,而从长期来看(去卵巢后14周),腔隙和小管直径减小。有趣的是,这些变化与空腔隙患病率增加同时出现,并且观察到骨细胞腔隙更呈圆形,腔隙空间周围有矿化边界。此外,我们报告MMP14+骨细胞增加,这也表明这些细胞有活跃的基质降解。这些结果共同提供了对雌激素缺乏期间皮质微孔隙率时间性变化的见解,并表明陷窝周围吸收和导致微石化的骨细胞凋亡均有可能发生。我们提出,微孔隙率变化是由不同群体的骨细胞驱动的过程引起的,这些骨细胞要么正在积极吸收其基质,要么已经经历凋亡并通过微石化作用填充腔隙。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5548/9156983/444e50124d6a/gr1.jpg

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