Yokota S, Atsumi S
Histochemistry. 1983;79(3):345-52. doi: 10.1007/BF00491770.
Immunoelectron microscopic localization of cathepsin D in rat nerve cells was investigated using protein A-gold technique. Brain and spinal cord were fixed by perfusion with 4% paraformaldehyde and 1% glutaraldehyde in 0.05 M cacodylate buffer. Vibratome sections of the cerebellum and spinal cord were embedded in Epon 812 or Lowicryl K4M. The postembedding immunocytochemical procedures with protein A-gold were applied to ultrathin sections. Gold particles representing the antigen sites of cathepsin D were localized in lysosomes of Purkinje cells and of presumed motorneurons in the anterior horn. A few gold particles were in Golgi stacks of these cells. The results indicate that the main subcellular domain for cathepsin D in rat nerve cells is lysosome.
采用蛋白A-金技术研究了组织蛋白酶D在大鼠神经细胞中的免疫电子显微镜定位。用含4%多聚甲醛和1%戊二醛的0.05M二甲胂酸盐缓冲液灌注固定脑和脊髓。将小脑和脊髓的振动切片包埋于Epon 812或Lowicryl K4M中。对超薄切片应用蛋白A-金的包埋后免疫细胞化学程序。代表组织蛋白酶D抗原位点的金颗粒定位于浦肯野细胞和前角假定运动神经元的溶酶体中。这些细胞的高尔基堆中有少量金颗粒。结果表明,大鼠神经细胞中组织蛋白酶D的主要亚细胞区域是溶酶体。