Lahr G, Heiss C, Mayerhofer A, Schilling K, Parmer R J, O'Connor D T, Gratzl M
Abteilung Anatomie und Zellbiologie, Universität Ulm, F.R.G.
Neuroscience. 1990;39(3):605-11. doi: 10.1016/0306-4522(90)90245-y.
The olfactory bulb of the rat contains chromogranin A at a similar level as the adrenal gland or the hypophysis as revealed by immunoblots. Olfactory chromogranin A also displays the same size as chromogranin A of endocrine cells. In the hippocampus and other brain regions, we could not detect chromogranin A by immunoblotting. In contrast, chromogranin A messenger ribonucleic acid (using S1 nuclease protection assays) was observed in all brain regions examined, including the olfactory bulb. By in situ hybridization histochemistry with a complementary ribonucleic acid probe (280 nucleotides), and by immunocytochemistry, chromogranin A synthesis could be localized to cell bodies of the mitral cell layer, of the external plexiform layer and of the periglomerular region of the olfactory bulb. Immunocytochemically, chromogranin A was also detected in the central projection areas of mitral and tufted cells in the primary olfactory cortex and the anterior amygdaloid area but not in the olfactory glomeruli, where the incoming olfactory nerve fibers of the primary olfactory neurons establish synaptic contacts. Taken together the data show that chromogranin A, following biosynthesis in the perikarya of the mitral and tufted cells, is specifically transported into their axonal terminals but not into their primary dendrites. We propose that the rat olfactory system could serve as a model for the study of chromogranin A regulation and function in neurons.
免疫印迹显示,大鼠嗅球中嗜铬粒蛋白A的含量与肾上腺或垂体中的含量相似。嗅嗜铬粒蛋白A的大小也与内分泌细胞的嗜铬粒蛋白A相同。在海马体和其他脑区,我们通过免疫印迹检测不到嗜铬粒蛋白A。相比之下,在包括嗅球在内的所有检测脑区中均观察到嗜铬粒蛋白A信使核糖核酸(使用S1核酸酶保护分析)。通过使用互补核糖核酸探针(280个核苷酸)的原位杂交组织化学和免疫细胞化学方法,嗜铬粒蛋白A的合成可定位于嗅球的二尖瓣细胞层、外丛状层和球周区域的细胞体。免疫细胞化学方法还在初级嗅觉皮层和杏仁前区的二尖瓣细胞和簇状细胞的中央投射区域检测到嗜铬粒蛋白A,但在初级嗅觉神经元传入的嗅觉神经纤维建立突触联系的嗅小球中未检测到。综合这些数据表明,嗜铬粒蛋白A在二尖瓣细胞和簇状细胞的胞体中生物合成后,被特异性地转运到它们的轴突终末,而不是它们的初级树突中。我们认为大鼠嗅觉系统可作为研究嗜铬粒蛋白A在神经元中的调节和功能的模型。