Fluorescent mapping of osteocyte-driven bone formation at pre-osteocyte and mature osteocyte lacunae.

IF 9.6
Sarah Ford, Kerstin Tiedemann, Rachel Shapiro, Svetlana V Komarova, Katharina Jähn-Rickert, Elizabeth A Zimmermann
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Abstract

Bone modeling and remodeling by osteoblasts and osteoclasts has been considered the primary mechanism of bone metabolism; however, osteocyte bone cells resorb their surrounding perilacunar bone matrix. It is unknown whether perilacunar remodeling contributes to bone formation in the absence of disease, disorder, or other external stimuli. Here, fluorescently labeled bone formation was quantified in femoral cortical bone and vertebral trabecular bone of skeletally mature female C57BL/6 mice (a commonly used mouse strain) using confocal microscopy. To explore whether the osteoblasts, pre-osteocytes, and mature osteocytes equally contributed to bone formation, the number density of lacunae with bone formation and bone formation rate were quantified. Bone formation was observed at both pre-osteocyte and mature osteocyte lacunae. In femoral cortical bone, 89% of lacunae with bone formation were mature osteocyte lacunae, while in vertebral trabecular bone, 32% of lacunae with bone formation were mature osteocyte lacunae. Bone formation rate at osteocyte lacunae was 1-2 orders of magnitude lower compared to osteoblast bone formation. Even though perilacunar (re)modeling has a smaller contribution to bone formation, it is important process that shapes the LCN in pre-osteocyte lacunae during the osteoblast-to-osteocyte transition and maintains bone quality in mature osteocyte lacunae. STATEMENT OF SIGNIFICANCE: Osteoclast and osteoblast bone cells have long been considered the cells responsible for bone remodeling. Here, we quantify the contributions of osteoblasts, pre-osteocytes, and mature osteocytes to bone metabolism in a common mouse strain. We find that perilacunar bone formation occurs at pre-osteocytes and mature osteocytes. In trabecular bone, a greater proportion of lacunae with bone formation were pre-osteocytes because trabecular bone has a high bone turnover. In cortical bone, a greater proportion of lacunae with bone formation were mature osteocytes. In the absence of disease or external stimuli, osteoblasts produce an order of magnitude more bone than at the perilacunar regions. However, perilacunar remodeling is still an important process regulating lacuno-canalicular network morphology and bone quality.

骨细胞驱动的骨形成在前骨细胞和成熟骨细胞腔隙的荧光定位。
成骨细胞和破骨细胞对骨的塑造和重塑被认为是骨代谢的主要机制;然而,骨细胞吸收其周围的腔周围骨基质。目前尚不清楚在没有疾病、紊乱或其他外部刺激的情况下,腔旁重构是否有助于骨形成。在这里,使用共聚焦显微镜,在骨骼成熟的雌性C57BL/6小鼠(一种常用的小鼠品系)的股骨皮质骨和椎小梁骨中定量荧光标记的骨形成。为了探讨成骨细胞、骨前细胞和成熟骨细胞对骨形成的贡献是否相同,我们对成骨腔隙的数量、密度和成骨率进行了量化。骨细胞前腔隙和成熟腔隙均可见骨形成。股骨皮质骨形成的腔隙89%为成熟骨细胞腔隙,而椎小梁骨形成的腔隙32%为成熟骨细胞腔隙。骨细胞腔隙成骨率比成骨细胞成骨率低1-2个数量级。尽管腔隙周围(再)建模对骨形成的贡献较小,但在成骨细胞向骨细胞转变过程中,形成前骨细胞腔隙中的LCN并维持成熟骨细胞腔隙中的骨质量是一个重要的过程。意义声明:破骨细胞和成骨细胞一直被认为是负责骨重塑的细胞。在这里,我们量化了成骨细胞、前骨细胞和成熟骨细胞对普通小鼠品系骨代谢的贡献。我们发现骨腔周围骨形成发生在骨前细胞和成熟骨细胞。在小梁骨中,由于小梁骨具有较高的骨更新率,骨形成的腔隙中有较大比例的骨前细胞。在皮质骨中,更大比例的骨形成腔隙是成熟的骨细胞。在没有疾病或外界刺激的情况下,成骨细胞产生的骨比在腔旁区域多出一个数量级。然而,腔隙周围重构仍然是调节腔隙网络形态和骨质量的重要过程。
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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