Garrison Institute on Aging, Department of Neurology, Texas Tech University Health Sciences Center, Lubbock, TX 79430, USA.
Microvasc Res. 2012 Mar;83(2):138-45. doi: 10.1016/j.mvr.2011.11.004. Epub 2011 Nov 10.
Hypoxia is increasingly recognized as an important contributing factor to the development of brain diseases such as Alzheimer's disease (AD). In the periphery, hypoxia is a powerful regulator of angiogenesis. However, vascular endothelial cells are remarkably heterogeneous and little is known about how brain endothelial cells respond to hypoxic challenge. The objective of this study is to characterize the effect of hypoxic challenge on the angiogenic response of cultured brain-derived microvascular endothelial cells. Brain endothelial cell cultures were initiated from isolated rat brain microvessels and subjected to hypoxia (1% O(2)) for various time periods. The results showed that hypoxia induced rapid (≤ 0.5h) expression of hypoxia-inducible factor 1α (HIF-1α) and that cell viability, assessed by MTT assay, was unaffected within the first 8h. Examination of brain endothelial cell cultures for pro- and anti-angiogenic proteins by western blot, RT-PCR and ELISA revealed that within 0.5 to 2h of hypoxia levels of vascular endothelial growth factor and endothelin-1 mRNA and protein were elevated. The expression of heme oxygenase-1 also increased but only after 8h of hypoxia. In contrast, similar hypoxia exposure evoked a decrease in endothelial nitric oxide synthase and thrombospondin-2 levels. Exposure of brain endothelial cell cultures to hypoxia resulted in a significant (p<0.001) decrease (94%) in tube length, an in vitro index of angiogenesis, compared to control cultures. The data indicate that, despite a shift toward a pro-angiogenic phenotype, hypoxia inhibited vessel formation in brain endothelial cells. These results suggest that in brain endothelial cells expression of angiogenic factors is not sufficient for the development of new vessels. Further work is needed to determine what factors/conditions prevent hypoxia-induced angiogenic changes from culminating in the formation of new brain blood vessels and what role this may play in the pathologic changes observed in AD and other diseases characterized by cerebral hypoxia.
缺氧越来越被认为是导致阿尔茨海默病(AD)等脑部疾病发展的重要因素。在周围环境中,缺氧是血管生成的强大调节剂。然而,血管内皮细胞具有显著的异质性,对于脑内皮细胞如何应对缺氧挑战知之甚少。本研究旨在描述缺氧对培养的脑源性微血管内皮细胞血管生成反应的影响。从分离的大鼠脑微血管中起始脑内皮细胞培养物,并使其经历各种时间的缺氧(1% O2)。结果表明,缺氧诱导了缺氧诱导因子 1α(HIF-1α)的快速(≤0.5h)表达,并且通过 MTT 测定法评估细胞活力在最初的 8h 内不受影响。通过 Western blot、RT-PCR 和 ELISA 检查脑内皮细胞培养物中的促血管生成和抗血管生成蛋白,发现缺氧 0.5 至 2h 后,血管内皮生长因子和内皮素-1 mRNA 和蛋白水平升高。血红素加氧酶-1的表达也增加,但仅在缺氧 8h 后。相比之下,类似的缺氧暴露会导致内皮型一氧化氮合酶和血栓素-2水平降低。与对照培养物相比,脑内皮细胞培养物暴露于缺氧会导致管长度(血管生成的体外指标)显著(p<0.001)减少(94%)。数据表明,尽管向促血管生成表型转变,但缺氧抑制了脑内皮细胞中的血管形成。这些结果表明,在脑内皮细胞中,血管生成因子的表达不足以形成新血管。需要进一步研究以确定哪些因素/条件阻止缺氧诱导的血管生成变化最终导致新的脑血管形成,以及这在 AD 和其他以脑缺氧为特征的疾病中观察到的病理变化中可能起什么作用。