Barres B A, Silverstein B E, Corey D P, Chun L L
Program in Neuroscience, Harvard Medical School, Boston, Massachusetts 02115.
Neuron. 1988 Nov;1(9):791-803. doi: 10.1016/0896-6273(88)90127-4.
Two different monoclonal antibodies to the Thy-1 antigen, T11D7 and 2G12, were used to purify and characterize retinal ganglion cells from postnatal rat retina. Although Thy-1 has been reported to be a specific marker for ganglion cells in retina, retinal cell suspensions contained several other types of Thy-1-positive cells as well. Nevertheless, a simple two-step "panning" procedure allowed isolation of ganglion cells to nearly 100% purity. We found that postnatal ganglion cells differed in antigenic, morphological, and intrinsic electrophysiological characteristics, and that these properties were correlated with one another. Minor variations of this panning protocol should allow rapid, high yield purification to homogeneity of many other neuronal and glial cell types.
使用两种针对Thy-1抗原的不同单克隆抗体T11D7和2G12,从新生大鼠视网膜中纯化并鉴定视网膜神经节细胞。尽管据报道Thy-1是视网膜神经节细胞的特异性标志物,但视网膜细胞悬液中也含有其他几种Thy-1阳性细胞类型。然而,一个简单的两步“淘选”程序可将神经节细胞分离至近100%的纯度。我们发现,新生神经节细胞在抗原、形态和内在电生理特性方面存在差异,且这些特性相互关联。该淘选方案的微小变化应能实现对许多其他神经元和神经胶质细胞类型的快速、高产纯化,使其达到均一性。