Davenport A P, Morton A J
Department of Medicine, University of Cambridge, Addenbrookes Hospital, U.K.
Brain Res. 1991 Jul 19;554(1-2):278-85. doi: 10.1016/0006-8993(91)90201-6.
Binding sites for iodinated endothelin (ET)-2, ET-3 and vasoactive intestinal contractor (VIC) were visualised in the adult rat brain using quantitative autoradiography and have a similar anatomical distribution to that of ET-1 and sarafotoxin S6b. Highest densities of binding sites for all 5 labelled peptides were present in the granular layer of the cerebellum. Cross-competition experiments show that at a concentration of 1 microM, unlabelled ET-1, ET-2, ET-3, VIC and sarafotoxin S6b were able to compete for the binding sites detected by each of the iodinated peptides. Binding sites for the ET isoforms were also present after 7-14 days in vitro in neurone-enriched primary cultures derived from embryonic rat cerebellum (16-18 days gestation) in which more than 90% of cells stained with an anti-neurofilament antibody. Using micro-autoradiography to detect the binding sites, an average of 14% of cells in these cultures with a diameter of 9.2 +/- 0.6 microns were associated with high silver grain densities (greater than 400 grains/100 microns). With some of these cells, silver grains were localised over cell bodies and branching processes characteristic of a neuronal phenotype. A second group of cells with high grain densities were more difficult to classify using morphological criteria and may be non-neuronal. The density of silver grains over the remaining cells was low (less than 20 grains/100 microns 2) and was similar to that measured in nuclear emulsion overlying cultures used to assess non-specific binding. These results indicate that binding sites for all ET peptides are present in both adult rat brain and embryonic cerebellar cultures.(ABSTRACT TRUNCATED AT 250 WORDS)
利用定量放射自显影技术,在成年大鼠脑中观察到了碘化内皮素(ET)-2、ET-3和血管活性肠收缩肽(VIC)的结合位点,其解剖分布与ET-1和sarafotoxin S6b相似。所有5种标记肽的结合位点密度在小脑颗粒层中最高。交叉竞争实验表明,在1 microM的浓度下,未标记的ET-1、ET-2、ET-3、VIC和sarafotoxin S6b能够竞争每种碘化肽检测到的结合位点。在体外培养7 - 14天后,来自胚胎大鼠小脑(妊娠16 - 18天)的富含神经元的原代培养物中也存在ET亚型的结合位点,其中超过90%的细胞用抗神经丝抗体染色。使用微放射自显影检测结合位点,这些培养物中平均直径为9.2 +/- 0.6微米的细胞中有14%与高银粒密度(大于400粒/100微米)相关。在其中一些细胞中,银粒定位于具有神经元表型特征的细胞体和分支过程上。另一组具有高粒密度的细胞根据形态学标准更难分类,可能是非神经元细胞。其余细胞上的银粒密度较低(小于20粒/100微米²),与用于评估非特异性结合的覆盖培养物的核乳剂中测得的密度相似。这些结果表明,所有ET肽的结合位点在成年大鼠脑和胚胎小脑培养物中均存在。(摘要截断于250字)