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{"title":"Multiphoton Imaging of Collagen, Elastin, and Calcification in Intact Soft-Tissue Samples","authors":"Piyusha S. Gade, Anne M. Robertson, Chih-Yuan Chuang","doi":"10.1002/cpcy.51","DOIUrl":null,"url":null,"abstract":"<p>Multiphoton-induced second-harmonic generation and two-photon excitation enable imaging of collagen and elastin fibers at micron-level resolution to depths of hundreds of microns, without the use of exogenous stains. These attributes can be leveraged for quantitative analysis of the 3D architecture of collagen and elastin fibers within intact, soft tissue specimens such as the artery and bladder wall. This architecture influences the function of intramural cells and also plays a primary role in determining tissue passive mechanical properties. Calcification deposition in soft tissues is a highly prevalent pathology in both older and diseased populations that can alter tissue properties. In this unit, we provide a protocol for simultaneous multiphoton microscopy (MPM) imaging and analysis of 3D collagen and elastin structures with calcification, which is effective for fixed and fresh intact samples. We also provide an associated micro-CT protocol to identify regions of interest in the samples as a means to target the MPM imaging. © 2018 by John Wiley & Sons, Inc.</p>","PeriodicalId":11020,"journal":{"name":"Current Protocols in Cytometry","volume":"87 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2018-10-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/cpcy.51","citationCount":"13","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current Protocols in Cytometry","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/cpcy.51","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"Health Professions","Score":null,"Total":0}
引用次数: 13
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Abstract
Multiphoton-induced second-harmonic generation and two-photon excitation enable imaging of collagen and elastin fibers at micron-level resolution to depths of hundreds of microns, without the use of exogenous stains. These attributes can be leveraged for quantitative analysis of the 3D architecture of collagen and elastin fibers within intact, soft tissue specimens such as the artery and bladder wall. This architecture influences the function of intramural cells and also plays a primary role in determining tissue passive mechanical properties. Calcification deposition in soft tissues is a highly prevalent pathology in both older and diseased populations that can alter tissue properties. In this unit, we provide a protocol for simultaneous multiphoton microscopy (MPM) imaging and analysis of 3D collagen and elastin structures with calcification, which is effective for fixed and fresh intact samples. We also provide an associated micro-CT protocol to identify regions of interest in the samples as a means to target the MPM imaging. © 2018 by John Wiley & Sons, Inc.
完整软组织标本中胶原蛋白、弹性蛋白和钙化的多光子成像
多光子诱导的二次谐波产生和双光子激发使胶原蛋白和弹性蛋白纤维在微米级分辨率下成像到数百微米深度,而无需使用外源染色剂。这些属性可以用于对完整软组织标本(如动脉和膀胱壁)内胶原蛋白和弹性蛋白纤维的3D结构进行定量分析。这种结构影响着壁内细胞的功能,也在决定组织被动力学性能方面起着主要作用。软组织钙化沉积在老年人和患病人群中都是一种非常普遍的病理,可以改变组织特性。在本单元中,我们提供了一种同时多光子显微镜(MPM)成像和分析具有钙化的三维胶原和弹性蛋白结构的方案,该方案适用于固定和新鲜完整的样品。我们还提供了一种相关的微ct方案,以确定样品中感兴趣的区域,作为靶MPM成像的手段。©2018 by John Wiley &儿子,Inc。
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