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通过沙鼠脑微血管内皮细胞与神经胶质细胞共培养在体外诱导血脑屏障的尝试。

Attempted induction of blood brain barrier in vitro by co-culture of gerbil brain microvessel endothelial cells and glial cells.

作者信息

Aiba T

机构信息

Department of Neurosurgery, Niigata University, Japan.

出版信息

Neurol Med Chir (Tokyo). 1995 Jun;35(6):347-52. doi: 10.2176/nmc.35.347.

DOI:10.2176/nmc.35.347
PMID:7566375
Abstract

The characteristics of isolated and subcultured Mongolian gerbil brain microvessel endothelial cells (BECs) were investigated, especially the disappearance of blood brain barrier (BBB) functions, and subcultured BECs were co-cultured with gerbil glial cells to assess a mass-producible BBB filter model. The subcultured cells lost specific characteristics observed in freshly isolated BECs, such as limited permeability to albumin and inulin, high gamma-glutamyl transpeptidase activity, and strong connections between individual cells. The subcultured BECs did not regain BBB functions during co-culture with glial cells, even derived from the same species. Only freshly isolated endothelial cells can be used for the BBB filter model, and a mass-producible BBB filter model may be impossible to make.

摘要

对分离培养的蒙古沙鼠脑微血管内皮细胞(BECs)的特性进行了研究,尤其关注血脑屏障(BBB)功能的丧失,并将传代培养的BECs与沙鼠神经胶质细胞共培养,以评估一种可大量生产的BBB过滤模型。传代培养的细胞失去了新鲜分离的BECs所具有的特定特性,如对白蛋白和菊粉的通透性有限、高γ-谷氨酰转肽酶活性以及单个细胞之间的紧密连接。传代培养的BECs在与神经胶质细胞共培养期间(即使这些神经胶质细胞来自同一物种)也没有恢复BBB功能。只有新鲜分离的内皮细胞可用于BBB过滤模型,且可能无法建立一种可大量生产的BBB过滤模型。

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