Schalling M, Stieg P E, Lindquist C, Goldstein M, Hökfelt T
Department of Histology, Karolinska Institutet, Stockholm, Sweden.
Proc Natl Acad Sci U S A. 1989 Jun;86(11):4302-5. doi: 10.1073/pnas.86.11.4302.
Thoracic ganglia in humans were studied after electrical, preganglionic stimulation using in situ hybridization with synthetic oligonucleotide probes against the catecholamine-synthesizing enzymes tyrosine hydroxylase (EC 1.14.16.2) and dopamine beta-hydroxylase (EC 1.14.17.1) and neuropeptide tyrosine. Immunohistochemical analysis was also performed. Following short peroperative stimulation a severalfold increase in all three mRNAs was found in principal ganglion cells, whereas no definite changes could be detected in enzyme or peptide levels with immunohistochemistry. The results suggest a very rapid and sensitive regulation of genes involved in signal transmission in the sympathetic nervous system of humans. Moreover, they indicate that electrical stimulation of neurons and/or pathways combined with in situ hybridization may be used as a method to define neuronal projections by visualizing increases in mRNAs for transmitter enzymes and/or peptide in target cells.
利用针对儿茶酚胺合成酶酪氨酸羟化酶(EC 1.14.16.2)、多巴胺β-羟化酶(EC 1.14.17.1)和神经肽Y的合成寡核苷酸探针进行原位杂交,对接受节前电刺激后的人体胸神经节进行了研究。还进行了免疫组织化学分析。在短期手术刺激后,主要神经节细胞中所有三种mRNA均出现数倍增加,而免疫组织化学检测未发现酶或肽水平有明确变化。结果表明,人体交感神经系统中参与信号传递的基因存在非常快速和敏感的调节。此外,这些结果表明,将神经元和/或神经通路的电刺激与原位杂交相结合,可作为一种通过可视化靶细胞中递质酶和/或肽的mRNA增加来确定神经元投射的方法。