Guerin J L, Bobilya D J
Department of Animal and Nutritional Sciences, University of New Hampshire, Durham 03824, USA.
Neurochem Res. 1997 Mar;22(3):321-6. doi: 10.1023/a:1022499023993.
The purpose of this study was to investigate the influence of hypothalamic extract, astrocyte coculture, and astrocyte-conditioned medium on the barrier function of an in vitro model of the blood-brain barrier. Porcine brain capillary endothelial cells were grown on polycarbonate membranes suspended between two chambers of media, representing the capillary lumen and brain interstitium. Endothelial cells grown alone and cocultured with astrocytes were cultured in growth medium with or without 50 micrograms/mL hypothalamic extract. An additional treatment consisted of endothelial cells cultured in growth medium that was first conditioned by astrocytes. Coculture consisted of a noncontact model with astrocytes attached to the bottom of the abluminal chamber. Barrier function of the endothelial cells was tested on days 1 through 9 post-seeding by measuring permeability to macromolecules (albumin) and small ions (electrical resistance). Resistance to the passage of macromolecules and small ions was greatest for endothelial cells grown without astrocytes in growth medium supplemented with hypothalamic extract. This barrier was maximal during days 4 through 7 post-seeding and was significantly less permeable than the barrier formed by endothelial cells grown in un-supplemented growth medium, in coculture with astrocytes, or in astrocyte-conditioned medium. These results demonstrate that a noncontact coculture with astrocytes did not enhance the integrity of this in vitro BBB model employing porcine brain capillary endothelial cells, but barrier function was increased when the model's medium was supplemented with hypothalamic extract.
本研究的目的是探讨下丘脑提取物、星形胶质细胞共培养以及星形胶质细胞条件培养基对血脑屏障体外模型屏障功能的影响。猪脑微血管内皮细胞生长在悬浮于两个培养基腔室之间的聚碳酸酯膜上,这两个腔室分别代表毛细血管腔和脑间质。单独培养的内皮细胞以及与星形胶质细胞共培养的内皮细胞在添加或不添加50微克/毫升下丘脑提取物的生长培养基中培养。另一种处理方式是将内皮细胞培养在预先由星形胶质细胞处理过的生长培养基中。共培养采用非接触模型,星形胶质细胞附着在无腔室的底部。在接种后的第1天至第9天,通过测量对大分子(白蛋白)和小离子(电阻)的通透性来测试内皮细胞的屏障功能。在添加下丘脑提取物的生长培养基中,未与星形胶质细胞共培养的内皮细胞对大分子和小离子通过的抵抗力最大。这种屏障在接种后的第4天至第7天达到最大,并且其通透性明显低于在未添加生长培养基中、与星形胶质细胞共培养或在星形胶质细胞条件培养基中生长的内皮细胞所形成的屏障。这些结果表明,与星形胶质细胞的非接触共培养并未增强采用猪脑微血管内皮细胞的这种体外血脑屏障模型的完整性,但当模型培养基中添加下丘脑提取物时,屏障功能增强。