Second Harmonic Generation Microscopy Differentiates Collagen Type I and Type III in COPD

被引:6
作者
Suzuki, Masaru [1 ]
Kayra, Damian [1 ]
Elliott, W. Mark [1 ]
Hogg, James C. [1 ]
Abraham, Thomas [1 ]
机构
[1] Univ British Columbia, Inst Heart Lung Hlth, UBC James Hogg Res Ctr, Vancouver, BC V6Z 1Y6, Canada
来源
MULTIPHOTON MICROSCOPY IN THE BIOMEDICAL SCIENCES XII | 2012年 / 8226卷
关键词
Second harmonic generation; fibrillar collagens; extracellular matrix; chronic obstructive pulmonary disease; emphysema; OBSTRUCTIVE PULMONARY-DISEASE; SMALL-AIRWAY OBSTRUCTION; ORGANIZATION; EMPHYSEMA; IMAGES;
D O I
10.1117/12.910815
中图分类号
TH742 [显微镜];
学科分类号
摘要
The structural remodeling of extracellular matrix proteins in peripheral lung region is an important feature in chronic obstructive pulmonary disease (COPD). Multiphoton microscopy is capable of inducing specific second harmonic generation (SHG) signal from non-centrosymmetric structural proteins such as fibrillar collagens. In this study, SHG microscopy was used to examine structural remodeling of the fibrillar collagens in human lungs undergoing emphysematous destruction (n=2). The SHG signals originating from these diseased lung thin sections from base to apex (n=16) were captured simultaneously in both forward and backward directions. We found that the SHG images detected in the forward direction showed well-developed and well-structured thick collagen fibers while the SHG images detected in the backward direction showed striking different morphological features which included the diffused pattern of forward detected structures plus other forms of collagen structures. Comparison of these images with the well-established immunohistochemical staining indicated that the structures detected in the forward direction are primarily the thick collagen type I fibers and the structures identified in the backward direction are diffusive structures of forward detected collagen type I plus collagen type III. In conclusion, we here demonstrate the feasibility of SHG microscopy in differentiating fibrillar collagen subtypes and understanding their remodeling in diseased lung tissues.
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页数:9
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