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Structure and quantification of microvascularisation within mouse long bones: What and how should we measure?

机译:小鼠长骨内微血管化的结构和定量:我们应该测量什么以及如何测量?

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Bone marrow vascularisation is involved in both remodeling and hematopo?esis. Challenged mouse models often require imaging and quantitative assessment of blood vessels and bone cell activities for a better understanding of the role of the vascular system. In this study we compared images of mouse hind limb long bone vascularisation after infusion of either barium sulfate or lead chromate-loaded silicon. The images were then analyzed through histology as well as low-resolution and synchrotron-radiation microtomography. We show that barium sulfate infusion provides the best vessel images and furthermore, that it is compatible with staining procedures used in bone histomorphometry and CD31 immunohistochemistry. Bone marrow vascularisation displays large structural and spatial distribution heterogeneity, including large lobular clusters of sinusoids and an unexpectedly substantial amount of capillaries in the adipocytes-rich distal third of the tibia. For an unbiased assessment of bone vascular development/changes, these features must be taken into account. We describe the conditions under which the quantification of microvascularisation on histological sections of barium-infused long bones is reproducible, as applied to seven-month-old male C57/Bl6J and mixed CD1/129Sv/J mice, and we propose a nomenclature for the histological parameters measured. Finally, we validate our technique by studying the effect of ovariectomy on mouse tibial vascular density.
机译:骨髓血管化参与重塑和造血。受到挑战的小鼠模型通常需要对血管和骨细胞活动进行成像和定量评估,以更好地了解血管系统的作用。在这项研究中,我们比较了注入硫酸钡或负载铬酸铅的硅后小鼠后肢长骨血管化的图像。然后通过组织学以及低分辨率和同步辐射显微断层摄影术对图像进行分析。我们显示硫酸钡输注可提供最佳血管图像,此外,它与骨组织形态测定法和CD31免疫组织化学中使用的染色程序兼容。骨髓血管化显示出较大的结构和空间分布异质性,包括正弦曲线的小叶簇和富含脂肪细胞的胫骨远端三分之一的毛细血管出乎意料的大量。对于骨血管发育/变化的无偏评估,必须考虑这些特征。我们描述了在重注入钡的长骨的组织切片上微血管化的定量可再现的条件,如适用于7个月大的雄性C57 / Bl6J和CD1 / 129Sv / J混合小鼠,我们提出了一种命名法测量组织学参数。最后,我们通过研究卵巢切除术对小鼠胫骨血管密度的影响来验证我们的技术。

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