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体内 3D 组织形态计量学定量分析骨形成和骨骼祖细胞分化。

In Vivo 3D Histomorphometry Quantifies Bone Apposition and Skeletal Progenitor Cell Differentiation.

机构信息

Department of Oral Medicine, Infection, and Immunity, Harvard School of Dental Medicine, Boston, MA, 02115, USA.

Advanced Microscopy Program, Center for Systems Biology and Wellman Center for Photomedicine, Massachusetts General Hospital, Harvard Medical School, Boston, MA, 02114, USA.

出版信息

Sci Rep. 2018 Apr 3;8(1):5580. doi: 10.1038/s41598-018-23785-6.

Abstract

Histomorphometry and Micro-CT are commonly used to assess bone remodeling and bone microarchitecture. These approaches typically require separate cohorts of animals to analyze 3D morphological changes and involve time-consuming immunohistochemistry preparation. Intravital Microscopy (IVM) in combination with mouse genetics may represent an attractive option to obtain bone architectural measurements while performing longitudinal monitoring of dynamic cellular processes in vivo. In this study we utilized two-photon, multicolor fluorescence IVM together with a lineage tracing reporter mouse model to image skeletal stem cells (SSCs) in their calvarial suture niche and analyze their differentiation fate after stimulation with an agonist of the canonical Wnt pathway (recombinant Wnt3a). Our in vivo histomorphometry analyses of bone formation, suture volume, and cellular dynamics showed that recombinant Wnt3a induces new bone formation, differentiation and incorporation of SSCs progeny into newly forming bone. IVM technology can therefore provide additional dynamic 3D information to the traditional static 2D histomorphometry.

摘要

组织形态计量学和微计算机断层扫描常用于评估骨重塑和骨微结构。这些方法通常需要对动物进行单独的分组,以分析 3D 形态变化,并涉及耗时的免疫组织化学准备。活体显微镜检查(IVM)与小鼠遗传学相结合,可能是一种有吸引力的选择,可以在体内进行动态细胞过程的纵向监测的同时,获得骨结构测量值。在这项研究中,我们利用双光子、多色荧光 IVM 以及谱系追踪报告小鼠模型,在颅骨缝合处成像骨骼干细胞(SSC),并分析它们在受到经典 Wnt 通路激动剂(重组 Wnt3a)刺激后的分化命运。我们对骨形成、缝合体积和细胞动力学的体内组织形态计量学分析表明,重组 Wnt3a 诱导新骨形成、分化和 SSC 后代掺入新形成的骨中。因此,IVM 技术可以为传统的静态 2D 组织形态计量学提供额外的动态 3D 信息。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/62e3/5882859/da9f679256e1/41598_2018_23785_Fig1_HTML.jpg

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