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本文引用的文献

1
Fabrication and operation of GRIN probes for in vivo fluorescence cellular imaging of internal organs in small animals.用于小动物体内器官荧光细胞成像的 GRIN 探头的制作和操作。
Nat Protoc. 2012 Jul 5;7(8):1456-69. doi: 10.1038/nprot.2012.078.
2
Intravital imaging.活体成像。
Cell. 2011 Nov 23;147(5):983-91. doi: 10.1016/j.cell.2011.11.004.
3
Stabilized imaging of immune surveillance in the mouse lung.稳定成像监测小鼠肺部的免疫监视。
Nat Methods. 2011 Jan;8(1):91-6. doi: 10.1038/nmeth.1543. Epub 2010 Dec 12.
4
Airway basal stem cells: a perspective on their roles in epithelial homeostasis and remodeling.气道基底干细胞:对其在上皮组织稳态和重塑中作用的展望。
Dis Model Mech. 2010 Sep-Oct;3(9-10):545-56. doi: 10.1242/dmm.006031. Epub 2010 Aug 10.
5
In vivo wide-area cellular imaging by side-view endomicroscopy.体腔内宽视场细胞内窥镜成像。
Nat Methods. 2010 Apr;7(4):303-5. doi: 10.1038/nmeth.1440. Epub 2010 Mar 14.
6
Real-time imaging of single cancer-cell dynamics of lung metastasis.实时成像观察肺癌转移的单细胞动力学。
J Cell Biochem. 2010 Jan 1;109(1):58-64. doi: 10.1002/jcb.22379.
7
Basal cells as stem cells of the mouse trachea and human airway epithelium.作为小鼠气管和人类气道上皮干细胞的基底细胞。
Proc Natl Acad Sci U S A. 2009 Aug 4;106(31):12771-5. doi: 10.1073/pnas.0906850106. Epub 2009 Jul 22.
8
The role of Scgb1a1+ Clara cells in the long-term maintenance and repair of lung airway, but not alveolar, epithelium.Scgb1a1⁺克拉拉细胞在肺气道而非肺泡上皮的长期维持和修复中的作用。
Cell Stem Cell. 2009 Jun 5;4(6):525-34. doi: 10.1016/j.stem.2009.04.002.
9
Real-time assessment of inflammation and treatment response in a mouse model of allergic airway inflammation.变应性气道炎症小鼠模型中炎症及治疗反应的实时评估
J Clin Invest. 2008 Dec;118(12):4058-66. doi: 10.1172/JCI36335. Epub 2008 Nov 6.
10
In vivo confocal and multiphoton microendoscopy.体内共聚焦和多光子显微内镜检查。
J Biomed Opt. 2008 Jan-Feb;13(1):010501. doi: 10.1117/1.2839043.

在气道再生过程中对小鼠气管上皮细胞的体内成像。

In vivo imaging of tracheal epithelial cells in mice during airway regeneration.

机构信息

Harvard Medical School, Massachusetts General Hospital, Boston, MA, USA.

出版信息

Am J Respir Cell Mol Biol. 2012 Dec;47(6):864-8. doi: 10.1165/rcmb.2012-0164OC. Epub 2012 Sep 13.

DOI:10.1165/rcmb.2012-0164OC
PMID:22984086
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3547097/
Abstract

Many human lung diseases, such as asthma, chronic obstructive pulmonary disease, bronchiolitis obliterans, and cystic fibrosis, are characterized by changes in the cellular composition and architecture of the airway epithelium. Intravital fluorescence microscopy has emerged as a powerful approach in mechanistic studies of diseases, but it has been difficult to apply this tool for in vivo respiratory cell biology in animals in a minimally invasive manner. Here, we describe a novel miniature side-view confocal probe capable of visualizing the epithelium in the mouse trachea in vivo at a single-cell resolution. We performed serial real-time endotracheal fluorescence microscopy in live transgenic reporter mice to view the three major cell types of the large airways, namely, basal cells, Clara cells, and ciliated cells. As a proof-of-concept demonstration, we monitored the regeneration of Clara cells over 18 days after a sulfur dioxide injury. Our results show that in vivo tracheal microscopy offers a new approach in the study of altered, regenerating, or metaplastic airways in animal models of lung diseases.

摘要

许多人类肺部疾病,如哮喘、慢性阻塞性肺疾病、闭塞性细支气管炎和囊性纤维化,其特征是气道上皮细胞的组成和结构发生变化。活体荧光显微镜已成为疾病机制研究的有力手段,但很难以微创的方式将该工具应用于动物体内的呼吸细胞生物学。在这里,我们描述了一种新型的微型侧视共聚焦探头,能够以单细胞分辨率对活体小鼠气管中的上皮进行成像。我们在活的转基因报告小鼠中进行了一系列实时气管内荧光显微镜检查,以观察大呼吸道的三种主要细胞类型,即基底细胞、克拉拉细胞和纤毛细胞。作为概念验证的演示,我们监测了二氧化硫损伤后 18 天克拉拉细胞的再生。我们的结果表明,活体气管显微镜为肺部疾病动物模型中气道改变、再生或化生的研究提供了一种新方法。