Origin of neomuscularized vessels in mice exposed to chronic hypoxia

被引:12
作者
Crnkovic, Slaven [1 ,2 ]
Hrzenjak, Andelko [3 ]
Marsh, Leigh M. [1 ]
Olschewski, Andrea [1 ,2 ]
Kwapiszewska, Grazyna [1 ]
机构
[1] Ludwig Boltzmann Inst Lung Vasc Res, A-8010 Graz, Austria
[2] Med Univ Graz, Univ Clin Anesthesiol & Intens Care Med, A-80363 Graz, Austria
[3] Med Univ Graz, Div Pulmonol, Dept Internal Med, A-8036 Graz, Austria
关键词
Chronic hypoxia; Pulmonary vascular remodeling; EphrinB2; EphB4; PULMONARY ARTERIAL-HYPERTENSION;
D O I
10.1016/j.resp.2011.09.016
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Exposure of mice to chronic hypoxia is one of the most often used animal models to study pulmonary hypertension. Hypoxia exposure leads to vascular remodeling and muscularization of the small parenchymal vessels in the lung. Due to the anatomical differences between mice and humans, it is not possible to determine whether the remodeled vessels originate from the arterial or venous side of the vasculature. By applying antibodies against specific marker molecules expressed by arterial (ephrinB2) and venous (EphB4) endothelial cells, we could show that remodeled parenchymal vessels in hypoxia-exposed mice are mostly of arterial origin with slight venous involvement. Using these tools, it is possible to further characterize remodeled vessels in other small animal models, such as transgenic or knockout mice. Particularly useful applications would include selection of parenchymal vessels for laser microdissection studies. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:342 / 345
页数:4
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