Oda Y, Okada Y, Katsuda S, Ikeda K, Nakanishi I
Department of Pathology, School of Medicine, Kanazawa University, Japan.
J Neurosci Methods. 1989 Jun;28(3):163-9. doi: 10.1016/0165-0270(89)90032-0.
We have developed a simple and relatively rapid method for obtaining a sufficient number of Schwann cells with a favorable purification ratio from newborn rat sciatic nerves. Perineurium-free nerves were torn into small fascicles of approximately 150-200 microns in diameter and explanted twice on type I collagen gel every 2 days of the culture period in order to reduce the number of contaminant fibroblasts. The last explanted tissues were fed with Dulbecco's modified Eagle medium supplemented with 10% fetal bovine serum and 100 micrograms/ml bovine pituitary extract for 10 days. More than 10 X 10(4) Schwann cells (greater than 95% purity) were obtained from newborn rat sciatic nerves.
我们已经开发出一种简单且相对快速的方法,可从新生大鼠坐骨神经中获得足够数量且纯化率良好的雪旺细胞。去除神经束膜的神经被撕成直径约150 - 200微米的小束,并在培养期间每隔2天将其接种于I型胶原凝胶上两次,以减少污染的成纤维细胞数量。最后一次接种的组织用添加了10%胎牛血清和100微克/毫升牛垂体提取物的杜尔贝科改良伊格尔培养基培养10天。从新生大鼠坐骨神经中获得了超过10×10⁴个雪旺细胞(纯度大于95%)。