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在骨内的天然环境中对活体内骨细胞的“三明治”结构进行可视化。

Visualizing the "sandwich" structure of osteocytes in their native environment deep in bone in vivo.

机构信息

Key Laboratory of Optoelectronic Devices and Systems of Ministry of Education and Guangdong Province, College of Optoelectronic Engineering, Shenzhen University, Shenzhen, China.

College of Physics and Energy, Shenzhen University, Shenzhen, China.

出版信息

J Biophotonics. 2019 Apr;12(4):e201800360. doi: 10.1002/jbio.201800360. Epub 2018 Dec 13.

Abstract

Osteocytes are the most abundant cells in bone and always the focus of bone research. They are embedded in the highly scattering mineralized bone matrix. Consequently, visualizing osteocytes deep in bone with subcellular resolution poses a major challenge for in vivo bone research. Here we overcome this challenge by demonstrating 3-photon imaging of osteocytes through the intact mouse skull in vivo. Through broadband transmittance characterization, we establish that the excitation at the 1700-nm window enables the highest optical transmittance through the skull. Using label-free third-harmonic generation (THG) imaging excited at this window, we visualize osteocytes through the whole 140-μm mouse skull and 155 μm into the brain in vivo. By developing selective labeling technique for the interstitial space, we visualize the "sandwich" structure of osteocytes in their native environment. Our work provides novel imaging methodology for bone research in vivo.

摘要

成骨细胞是骨组织中最丰富的细胞,一直是骨研究的重点。它们嵌入在高度散射的矿化骨基质中。因此,对活体骨研究来说,要实现亚细胞分辨率的深层骨内成骨细胞可视化是一项重大挑战。在这里,我们通过在活体小鼠颅骨中演示 3 光子成骨细胞成像来克服这一挑战。通过宽带透过率特性分析,我们确定在 1700nm 窗口处的激发可以实现颅骨的最高光透过率。我们使用在此窗口处激发的无标记的三次谐波产生(THG)成像,对活体小鼠颅骨中的 140μm 以及 155μm 深度的脑组织进行成骨细胞可视化。通过开发用于间质空间的选择性标记技术,我们可以在其天然环境中可视化成骨细胞的“三明治”结构。我们的工作为活体骨研究提供了新的成像方法。

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