A METHOD FOR THE ISOLATION AND CULTURE OF RAT PERIPHERAL-NERVE VASCULAR ENDOTHELIAL-CELLS

被引:15
作者
ARGALL, KG [1 ]
ARMATI, PJ [1 ]
POLLARD, JD [1 ]
机构
[1] UNIV SYDNEY,DEPT NEUROL,SYDNEY,NSW 2006,AUSTRALIA
关键词
D O I
10.1006/mcne.1994.1051
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
In studying autoimmune diseases of the human peripheral nervous system (PNS), in vitro studies involving the use of cultured rat Schwann cells, neurons, and disease-inducing immune system cells have provided basic information about disease pathogenesis. For example, T-cells that induce experimental allergic neuritis have been shown in vitro to damage Schwann cells, the target cell in these diseases. However, before making contact with Schwann cells, these T-cells must first pass through the blood-nerve barrier. Despite the importance of this interaction, no studies employing PNS endothelial cells in coculture with dorsal root ganglia cells to mimic the environment of the blood-nerve barrier have been reported. This paper describes a simple method for the isolation and culture of peripheral nerve vascular endothelial cells from adult rats that should facilitate in vitro studies of the blood-nerve barrier. Endothelial cells were identified by their expression of an endothelial cell marker, Factor VIII/von Willebrand factor. Their identity was further confirmed by their inability to express Thy 1.1, a fibroblast marker, and their in vitro morphology. Purity of endothelial cell cultures was ensured by a regular program of Thy 1.1 complement depletion of fibroblasts. (C) 1994 Academic Press, Inc.
引用
收藏
页码:413 / 417
页数:5
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