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首页> 外文期刊>Acta Histochemica: Zeitschrift fur Histologische Topochemie >Differences in the expression of catecholamine-synthesizing enzymes between vesicular monoamine transporter 1-and 2-immunoreactive glomus cells in the rat carotid body
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Differences in the expression of catecholamine-synthesizing enzymes between vesicular monoamine transporter 1-and 2-immunoreactive glomus cells in the rat carotid body

机译:大鼠颈动脉体内脉络膜单胺转运蛋白1-和2-免疫反应性肾小球细胞在大鼠颈动脉体中表达儿茶胺合成酶的差异

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摘要

Vesicular monoamine transporters (VMAT) 1 and 2 are responsible for monoamine transportation into secretary vesicles and are tissue-specifically expressed in central and peripheral monoaminergic tissues, including the carotid body (CB). The aim of the present study was to examine the expression of catecholamine-synthesizing enzymes in VMAT1- and VMAT2-immunoreactive glomus cells in the rat CB using multiple immunolabeling. The expression of VMAT1 and VMAT2 mRNA in the CB was confirmed by RT-PCR. Immunohistochemistry revealed that VMAT1 immunoreactivity was predominant in glomus cells rather than VMAT2 immunoreactivity. Glomus cells with VMAT1 immunoreactivity exhibited weak/negative VMAT2 immunoreactivity, and vice versa. Immunoreactivities for VMAT1 and tyrosine hydroxylase, the rate-limiting enzyme for catecholamine biosynthesis, were co-localized in the same glomus cells and a positive correlation was confirmed between the two immunoreactivities (Spearman's coefficient = 0.82; p < 0.05). Although some glomus cells showed co-localization of VMAT2 and dopamine beta-hydroxylase immunoreactivity, the biosynthetic enzyme for noradrenaline, VMAT2 immunoreactivity appeared to be less associated with both catecholamine-synthesizing enzymes as indicated by a correlation analysis (TH: Spearman's coefficient = 0.38, DBH: Spearman's coefficient = 0.26). These results indicate that heterogeneity on functional role would exist among glomus cells in terms of VMAT isoform and catecholamine-synthesizing enzymes expression.
机译:尿素单胺转运蛋白(VMAT)1和2负责单胺运输到秘书囊泡中,并在中环和外周单氨基能组织中表达组织,包括颈动脉体(CB)。本研究的目的是使用多种免疫标记检查大鼠CB中的VMAT1和VMAT2-免疫反应性肾小球细胞中儿茶酚胺合成酶的表达。通过RT-PCR确认CB中VMAT1和VMAT2 mRNA的表达。免疫组织化学揭示了VMAT1免疫反应性在Glomus细胞中占主导地位,而不是VMAT2免疫反应性。具有VMAT1免疫反应性的Glomus细胞表现出弱/阴性VMAT2免疫反应性,反之亦然。 VMAT1和酪氨酸羟化酶的免疫反应性,用于儿茶酚胺生物合成的速率限制酶,在相同的肾小球细胞中共同定位,两种免疫反应(Spearman系数= 0.82; P <0.05)确认阳性相关性。虽然一些Glomus细胞显示VMAT2和多巴胺β-羟化酶免疫反应性的共定位,但是对于去甲肾上腺素的生物合成酶,VMAT2免疫反应性似乎与由相关分析(TH:Spearman的系数= 0.38的CateCholamine合成酶较少相关DBH:Spearman的系数= 0.26)。这些结果表明,在VMAT同种型和儿茶酚酰胺合成酶表达中,Glomus细胞中存在对功能作用的异质性。

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