Division of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA 91125, USA.
Endocrine Unit, Massachusetts General Hospital, Harvard Medical School, Boston, MA 02114, USA.
Sci Transl Med. 2017 Apr 26;9(387). doi: 10.1126/scitranslmed.aah6518.
Bone tissue harbors unique and essential physiological processes, such as hematopoiesis, bone growth, and bone remodeling. To enable visualization of these processes at the cellular level in an intact environment, we developed "Bone CLARITY," a bone tissue clearing method. We used Bone CLARITY and a custom-built light-sheet fluorescence microscope to detect the endogenous fluorescence of Sox9-tdTomato osteoprogenitor cells in the tibia, femur, and vertebral column of adult transgenic mice. To obtain a complete distribution map of these osteoprogenitor cells, we developed a computational pipeline that semiautomatically detects individual Sox9-tdTomato cells in their native three-dimensional environment. Our computational method counted all labeled osteoprogenitor cells without relying on sampling techniques and displayed increased precision when compared with traditional stereology techniques for estimating the total number of these rare cells. We demonstrate the value of the clearing-imaging pipeline by quantifying changes in the population of Sox9-tdTomato-labeled osteoprogenitor cells after sclerostin antibody treatment. Bone tissue clearing is able to provide fast and comprehensive visualization of biological processes in intact bone tissue.
骨组织具有独特而重要的生理过程,如造血、骨生长和骨重塑。为了在完整的环境中实现这些过程在细胞水平上的可视化,我们开发了“Bone CLARITY”,一种骨组织透明化方法。我们使用 Bone CLARITY 和定制的光片荧光显微镜来检测成年转基因小鼠胫骨、股骨和脊柱中 Sox9-tdTomato 成骨前体细胞的内源性荧光。为了获得这些成骨前体细胞的完整分布图,我们开发了一种计算管道,该管道可在其天然的三维环境中半自动检测单个 Sox9-tdTomato 细胞。我们的计算方法无需依赖采样技术即可计算所有标记的成骨前体细胞,并且与传统的用于估计这些稀有细胞总数的体视学技术相比,显示出更高的精度。我们通过量化硬化蛋白抗体治疗后 Sox9-tdTomato 标记的成骨前体细胞群体的变化,证明了清除成像管道的价值。骨组织透明化能够快速全面地观察完整骨组织中的生物学过程。