A method for the isolation and culture of rat peripheral nerve vascular endothelial cells.

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.