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离体猪眼的多光子自发荧光和二次谐波产生成像

Multiphoton autofluorescence and second-harmonic generation imaging of the ex vivo porcine eye.

作者信息

Teng Shu-Wen, Tan Hsin-Yuan, Peng Ju-Li, Lin Huei-Hsing, Kim Ki Hean, Lo Wen, Sun Yen, Lin Wei-Chou, Lin Sung-Jan, Jee Shiou-Hwa, So Peter T C, Dong Chen-Yuan

机构信息

Microscopic Biophysics Laboratory, Department of Physics, National Taiwan University, Teipei.

出版信息

Invest Ophthalmol Vis Sci. 2006 Mar;47(3):1216-24. doi: 10.1167/iovs.04-1520.

Abstract

PURPOSE

The purpose of this work was to demonstrate the use of the combined imaging modality of multiphoton autofluorescence and second-harmonic generation (SHG) microscopy in obtaining spectrally resolved morphologic features of the cornea, limbus, conjunctiva, and sclera in whole, ex vivo porcine eyes.

METHODS

The 780-nm output of a femtosecond, titanium-sapphire laser was used to induce broadband autofluorescence (435-700 nm) and SHG (390 nm) from various regions of the surface of ex vivo porcine eyes. A water-immersion objective was used for convenient imaging of the curved surface of the eye.

RESULTS

Multiphoton autofluorescence was useful in identifying cellular structures of the different domains of the ocular surface, and the SHG signal can be used to resolve collagen organization within the cornea stroma and sclera of ex vivo porcine eyes.

CONCLUSIONS

Multiphoton autofluorescence and SHG microscopy have been demonstrated to be an effective technique for resolving, respectively, the cellular and collagen structures within the ocular surface of ex vivo porcine eyes. SHG imaging resolved the difference in structural orientations between corneal and sclera collagen fibers. Specifically, the corneal collagen is organized in a depth-dependent fashion, whereas the scleral collagen is randomly packed. Because this technique does not require histologic preparation procedures, it has the potential to be applied for in vivo studies with minimal disturbance to the eye.

摘要

目的

本研究旨在展示多光子自发荧光和二次谐波产生(SHG)显微镜联合成像模式在获取完整的离体猪眼角膜、角膜缘、结膜和巩膜的光谱分辨形态特征方面的应用。

方法

使用飞秒钛宝石激光器780 nm的输出光,诱导离体猪眼表面不同区域产生宽带自发荧光(435 - 700 nm)和SHG(390 nm)。使用水浸物镜以便对眼睛的曲面进行便捷成像。

结果

多光子自发荧光有助于识别眼表不同区域的细胞结构,SHG信号可用于分辨离体猪眼角膜基质和巩膜内的胶原组织。

结论

多光子自发荧光和SHG显微镜已被证明是一种有效的技术,分别用于分辨离体猪眼眼表的细胞和胶原结构。SHG成像分辨了角膜和巩膜胶原纤维结构取向的差异。具体而言,角膜胶原以深度依赖的方式排列,而巩膜胶原则随机堆积。由于该技术不需要组织学制备程序,因此有潜力应用于体内研究,对眼睛的干扰最小。

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