Quantification of collagen fiber structure using second harmonic generation imaging and two-dimensional discrete Fourier transform analysis: Application to the human optic nerve head

被引:29
作者
Pijanka, Jacek K. [1 ]
Markov, Petar P. [1 ]
Midgett, Dan [2 ,3 ]
Paterson, Neil G. [4 ]
White, Nick [5 ]
Blain, Emma J. [6 ]
Thao D Nguyen [2 ,3 ]
Quigley, Harry A. [7 ]
Boote, Craig [1 ]
机构
[1] Cardiff Univ, Sch Optometry & Vis Sci, Struct Biophys Grp, Cardiff, S Glam, Wales
[2] Johns Hopkins Univ, Dept Mech Engn, Baltimore, MD 21218 USA
[3] Johns Hopkins Univ, Dept Mat Sci, Baltimore, MD USA
[4] Diamond Light Source, MX Div, Harwell Sci & Innovat Campus, Harwell, Berks, England
[5] Cardiff Univ, Sch Optometry & Vis Sci, Vivat Scientia Bioimaging Labs, Cardiff, S Glam, Wales
[6] Cardiff Univ, Arthrit Res UK Biomech & Bioengn Ctr, Cardiff, S Glam, Wales
[7] Johns Hopkins Univ, Sch Med, Wilmer Ophthalmol Inst, Glaucoma Ctr Excellence, Baltimore, MD 21205 USA
基金
英国工程与自然科学研究理事会; 美国国家卫生研究院;
关键词
collagen fiber structure; discrete Fourier transform; edge effect artefact correction; nonlinear microscopy; optic nerve head; second harmonic generation; LAMINA-CRIBROSA; CORNEAL COLLAGEN; ORGANIZATION; ORIENTATION; MICROSCOPY; MATRIX; SCLERA; SUSCEPTIBILITY; GLAUCOMA; FIBRILS;
D O I
10.1002/jbio.201800376
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Second harmonic generation (SHG) microscopy is widely used to image collagen fiber microarchitecture due to its high spatial resolution, optical sectioning capabilities and relatively nondestructive sample preparation. Quantification of SHG images requires sensitive methods to capture fiber alignment. This article presents a two-dimensional discrete Fourier transform (DFT)-based method for collagen fiber structure analysis from SHG images. The method includes integrated periodicity plus smooth image decomposition for correction of DFT edge discontinuity artefact, avoiding the loss of peripheral image data encountered with more commonly used windowing methods. Outputted parameters are as follows: the collagen fiber orientation distribution, aligned collagen content and the degree of collagen fiber dispersion along the principal orientation. We demonstrate its application to determine collagen microstructure in the human optic nerve head, showing its capability to accurately capture characteristic structural features including radial fiber alignment in the innermost layers of the bounding sclera and a circumferential collagen ring in the mid-stromal tissue. Higher spatial resolution rendering of individual lamina cribrosa beams within the nerve head is also demonstrated. Validation of the method is provided in the form of correlative results from wide-angle X-ray scattering and application of the presented method to other fibrous tissues.
引用
收藏
页数:19
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