Quantitative microscopy in murine models of lung inflammation.

Joseph Soltzberg, Sarah Frischmann, Christiaan van Heeckeren, Nicole Brown, Arnold Caplan, Tracey L Bonfield
{"title":"Quantitative microscopy in murine models of lung inflammation.","authors":"Joseph Soltzberg,&nbsp;Sarah Frischmann,&nbsp;Christiaan van Heeckeren,&nbsp;Nicole Brown,&nbsp;Arnold Caplan,&nbsp;Tracey L Bonfield","doi":"","DOIUrl":null,"url":null,"abstract":"<p><strong>Objective: </strong>To develop a quantitative means to measure lung inflammation using the murine models of chronic asthma and cystic fibrosis (CF).</p><p><strong>Study design: </strong>Translational-based medicine often utilizes animal models to study new and innovative therapeutics. In asthma and CF, the animal models focus on airway inflammation and remodeling. The asthma model is based on hypersensitivity-induced airway disease, whereas the CF model focuses on the inflammatory response to infection with Pseudomonas aeruginosa. Qualitative measures of inflammation and lung pathophysiology introduce significant variability and difficulty in interpreting interventional outcomes. The highly sensitive and reproducible quantitative computational program interfaced with Image Pro Microscopy to monitor changes in lung inflammation and lung pathophysiology. The software interfaces with image microscopy and automates the lung section review process.</p><p><strong>Results: </strong>Results from this program recapitulated data obtained by manual point counting of inflammation, bronchoalveolar lavage differential, and histology. The data show a low coefficient of variation and high reproducibility between slides and sections.</p><p><strong>Conclusion: </strong>Utilization of this new microscopy program will enhance the quantitative means of establishing changes in lung structure and inflammation as a measure of therapeutic intervention with the ability of refining interpretation of in vivo models potentially short-circuiting translation into the clinical setting.</p>","PeriodicalId":76995,"journal":{"name":"Analytical and quantitative cytology and histology","volume":"33 5","pages":"245-52"},"PeriodicalIF":0.0000,"publicationDate":"2011-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4195243/pdf/nihms-627926.pdf","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Analytical and quantitative cytology and histology","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Objective: To develop a quantitative means to measure lung inflammation using the murine models of chronic asthma and cystic fibrosis (CF).

Study design: Translational-based medicine often utilizes animal models to study new and innovative therapeutics. In asthma and CF, the animal models focus on airway inflammation and remodeling. The asthma model is based on hypersensitivity-induced airway disease, whereas the CF model focuses on the inflammatory response to infection with Pseudomonas aeruginosa. Qualitative measures of inflammation and lung pathophysiology introduce significant variability and difficulty in interpreting interventional outcomes. The highly sensitive and reproducible quantitative computational program interfaced with Image Pro Microscopy to monitor changes in lung inflammation and lung pathophysiology. The software interfaces with image microscopy and automates the lung section review process.

Results: Results from this program recapitulated data obtained by manual point counting of inflammation, bronchoalveolar lavage differential, and histology. The data show a low coefficient of variation and high reproducibility between slides and sections.

Conclusion: Utilization of this new microscopy program will enhance the quantitative means of establishing changes in lung structure and inflammation as a measure of therapeutic intervention with the ability of refining interpretation of in vivo models potentially short-circuiting translation into the clinical setting.

小鼠肺部炎症模型的定量显微镜观察。
目的:建立慢性哮喘和囊性纤维化(CF)小鼠模型肺部炎症的定量测量方法。研究设计:转化医学经常利用动物模型来研究新的和创新的治疗方法。在哮喘和CF中,动物模型主要关注气道炎症和重塑。哮喘模型基于超敏性气道疾病,而CF模型侧重于铜绿假单胞菌感染后的炎症反应。炎症和肺病理生理的定性测量引入了显著的可变性和解释介入结果的困难。高度敏感和可重复的定量计算程序与Image Pro显微镜相结合,监测肺部炎症和肺部病理生理的变化。该软件接口与图像显微镜和自动肺切片审查过程。结果:该程序的结果概括了炎症、支气管肺泡灌洗鉴别和组织学的手工点状计数。数据显示低变异系数和高再现性之间的幻灯片和切片。结论:利用这种新的显微镜程序将加强定量手段,建立肺结构和炎症的变化,作为治疗干预的衡量标准,并有能力完善体内模型的解释,可能会缩短转化为临床环境的时间。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信