Department of Biomedical Engineering, P.O. Box 800759, UVA Health System, Charlottesville, VA 22908, USA.
Microvasc Res. 2010 Mar;79(2):93-101. doi: 10.1016/j.mvr.2010.01.006. Epub 2010 Jan 18.
Currently, little is known about the response of the adult retinal microvasculature to hypoxia. To test the hypothesis that chronic systemic hypoxia induces angiogenesis and microvascular remodeling in the adult mouse retina, adult 10-week old female C57Bl/6 mice were exposed to 10% O(2) for 2 or 3 weeks. After hypoxia exposure, retinas were harvested, whole-mounted, and processed for immunohistochemistry. Retinas were stained with lectin, anti-smooth muscle alpha-actin antibody, and anti-NG2 antibody to visualize microvascular networks and their cellular components. Confocal microscopy was used to obtain images of superficial retinal networks. Images were analyzed to assess vessel diameter, vascular length density, branch point density, and the presence of vascular loops, a hallmark of intussusceptive angiogenesis. Both 2 and 3 weeks of hypoxia exposure resulted in a significant increase in the diameters of arterioles and post-arteriole capillaries (p<0.003). After 3 weeks of hypoxia, vascular length density and branch point density were significantly increased in retinas exposed to hypoxia as compared to normoxic controls (p<0.001). The number of vascular loops in the superficial retinal networks was significantly greater in hypoxia-exposed retinas (p < or = 0.001). Our results demonstrate, for the first time, intussusceptive angiogenesis as a tissue-level mechanism of vascular adaptation to chronic systemic hypoxia in the adult mouse retina and contribute to our understanding of hypoxia-induced angiogenesis and microvascular remodeling in the adult animal.
目前,人们对成年视网膜微血管对缺氧的反应知之甚少。为了验证慢性系统性缺氧会诱导成年小鼠视网膜血管生成和微血管重塑的假设,将成年 10 周龄雌性 C57Bl/6 小鼠暴露于 10%的 O(2)中 2 或 3 周。在缺氧暴露后,收获视网膜,全铺片,并进行免疫组织化学处理。用凝集素、抗平滑肌α-肌动蛋白抗体和抗-NG2 抗体对视网膜进行染色,以可视化微血管网络及其细胞成分。共聚焦显微镜用于获取浅层视网膜网络的图像。分析图像以评估血管直径、血管长度密度、分支点密度以及血管环的存在,这是内套叠血管生成的标志。2 周和 3 周的缺氧暴露都导致小动脉和小动脉后毛细血管的直径显著增加(p<0.003)。在缺氧 3 周后,与正常氧对照组相比,缺氧暴露的视网膜中血管长度密度和分支点密度显著增加(p<0.001)。在缺氧暴露的视网膜中,浅层视网膜网络中的血管环数量显著增加(p < or = 0.001)。我们的研究结果首次证明,在成年小鼠视网膜中,内套叠血管生成是血管适应慢性系统性缺氧的组织水平机制,并有助于我们理解成年动物中缺氧诱导的血管生成和微血管重塑。