Haselton F R, Dworska E, Evans S S, Hoffman L H, Alexander J S
Department of Biomedical Engineering, Vanderbilt University, Nashville, TN 37235, USA.
Exp Eye Res. 1996 Aug;63(2):211-22. doi: 10.1006/exer.1996.0110.
The prediabetic/diabetic condition functionally alters the microvascular bed of the eye and the breakdown in the transvascular barrier may be produced by changes in the retinal endothelial barrier. To better understand how retinal microvessel barrier is maintained and is altered in vivo this study applies and extends our previously described in vitro permeability technique to study retinal endothelial monolayers. The model of the retinal microvasculature consists of retinal capillary endothelial cells cultured on porous microcarrier beads and perfused in chromatographic 'cell-columns'. This model design relies on indicator-dilution techniques to measure the permeability of the retinal endothelial monolayer and detects small changes in retinal endothelial permeability produced by treatments. Bovine retinal capillary endothelial cells (RCE) were obtained using an endothelial selective media. RCE were seeded at 3 x 10(4) cells cm-2 of fibronectin-coated gelatin microcarriers. After 7 days of microcarrier culture, microcarriers were poured to form columns 0.66 cm in diameter and 1.6 cm in length. The cell-column elution patterns of coinjected optically absorbing tracers (blue dextran 2 x 10(6) Da; cyanocobalamin 1355 Da; sodium fluorescein 376 Da) were analysed to estimate the permeability of the RCE monolayers covering the microcarriers. Scanning electron microscopic examination showed complete monolayer formation on the surface of the microcarriers. We found that baseline monolayer permeability averaged 7.57 +/- 0.57 x 10(-5) cm sec-1 for cyanocobalamin and 9.29 +/- 0.78 x 10(-5) cm sec-1 for sodium fluorescein (mean +/- S.E.M., n = 39). Permeability did not increase over 2 hr of cell-column perfusion. Permeability was decreased by 1 micron isoproterenol (n = 3) and increased by 1 microgram ml-1 cytochalasin D (n = 5). This is one of the first reports of in vitro permeability values for the transport barrier formed by retinal microvascular endothelial cells. Furthermore, the endothelial component of the retinal barrier is dynamic, and is enhanced by isoproterenol and diminished by cytochalasin D.
糖尿病前期/糖尿病状态会在功能上改变眼部的微血管床,而视网膜内皮屏障的变化可能导致跨血管屏障的破坏。为了更好地理解视网膜微血管屏障在体内是如何维持和改变的,本研究应用并扩展了我们之前描述的体外通透性技术来研究视网膜内皮单层。视网膜微血管模型由培养在多孔微载体珠上并在色谱“细胞柱”中灌注的视网膜毛细血管内皮细胞组成。该模型设计依靠指示剂稀释技术来测量视网膜内皮单层的通透性,并检测处理引起的视网膜内皮通透性的微小变化。使用内皮细胞选择性培养基获得牛视网膜毛细血管内皮细胞(RCE)。将RCE以3×10⁴个细胞/cm²的密度接种在纤连蛋白包被的明胶微载体上。微载体培养7天后,将微载体倒入以形成直径0.66 cm、长度1.6 cm的柱。分析共注射的光学吸收示踪剂(2×10⁶ Da的蓝色葡聚糖;1355 Da的氰钴胺素;376 Da的荧光素钠)的细胞柱洗脱模式,以估计覆盖微载体的RCE单层的通透性。扫描电子显微镜检查显示微载体表面形成了完整的单层。我们发现,氰钴胺素的基线单层通透性平均为7.57±0.57×10⁻⁵ cm/秒,荧光素钠的基线单层通透性平均为9.29±0.78×10⁻⁵ cm/秒(平均值±标准误,n = 39)。在细胞柱灌注2小时内通透性没有增加。1 μM异丙肾上腺素可降低通透性(n = 3),1 μg/ml细胞松弛素D可增加通透性(n = 5)。这是关于视网膜微血管内皮细胞形成的转运屏障的体外通透性值的首批报告之一。此外,视网膜屏障的内皮成分是动态的,异丙肾上腺素可增强其功能,细胞松弛素D可减弱其功能。