小鼠纤维化模型中血管生成和肺泡-毛细血管网络可视化和定量新技术的发展。

IF 3.5 2区 医学 Q1 PHYSIOLOGY
Hannah F Thorndyke, Evan P Lundberg, Edwin Ortiz Gaxon, Maggie M Dawson, Emma C Mason, Julia M Hollaway, Eszter K Vladar, David Coronado Escobar, Susan M Majka
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引用次数: 0

摘要

适应性血管生成可以驱动修复或组织重塑的发病机制。肺血管功能障碍是慢性肺部疾病(CLD)的主要表现,但血管生成在慢性肺部疾病发展中的作用尚不明确。肺泡毛细血管网络中的微血管毛细血管是肺部受修剪和重塑影响最大的血管,导致毛细血管长度和直径减少,随后气体交换面损失。我们的实验室先前已经证明微血管内皮祖细胞(mvEPCs)驱动修复性血管生成。我们假设肺泡-毛细血管的三维可视化对于确定CLD的修复与进展机制至关重要。为了解决这一知识空白,我们开发了一种简单可靠的荧光灌注技术,可以使用肺损伤小鼠模型定量肺泡毛细血管网络中的微血管结构。该方法可用于各种器官系统,以可视化微血管结构及其在疾病中的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Development of novel technology for the visualization and quantitation of angiogenesis and the alveolar-capillary network in a mouse model of fibrosis.

Adaptive angiogenesis can drive repair or underlie the pathogenesis of tissue remodeling. Pulmonary vascular dysfunction is a major manifestation of chronic lung disease (CLD), but the role of angiogenesis in the development of CLD is not well defined. Microvascular capillaries in the alveolar-capillary network are the vessels most affected by pruning and remodeling in the lung, resulting in reduced capillary length and diameter with subsequent loss of gas exchange surfaces. Our lab has previously demonstrated that microvascular endothelial progenitor cells (mvEPCs) drive reparative angiogenesis. We hypothesize that visualization of the alveolar-capillary microvasculature in three-dimensions is essential to define the mechanisms governing repair versus progression to the pathogenesis of CLD. To address this gap in knowledge, we have developed a simple and reliable fluorescent perfusion technique that will allow the quantitation of microvessel structure in the alveolar-capillary network using mouse models of lung injury. This approach may be used in various organ systems to visualize microvasculature structure and its role in disease.NEW & NOTEWORTHY We developed and validated a fluorescent technology to visualize and quantify the alveolar-capillary network in three-dimensions in mouse lung for modeling of the microvasculature in models of lung disease.

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来源期刊
CiteScore
9.20
自引率
4.10%
发文量
146
审稿时长
2 months
期刊介绍: The American Journal of Physiology-Lung Cellular and Molecular Physiology publishes original research covering the broad scope of molecular, cellular, and integrative aspects of normal and abnormal function of cells and components of the respiratory system. Areas of interest include conducting airways, pulmonary circulation, lung endothelial and epithelial cells, the pleura, neuroendocrine and immunologic cells in the lung, neural cells involved in control of breathing, and cells of the diaphragm and thoracic muscles. The processes to be covered in the Journal include gas-exchange, metabolic control at the cellular level, intracellular signaling, gene expression, genomics, macromolecules and their turnover, cell-cell and cell-matrix interactions, cell motility, secretory mechanisms, membrane function, surfactant, matrix components, mucus and lining materials, lung defenses, macrophage function, transport of salt, water and protein, development and differentiation of the respiratory system, and response to the environment.
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