Pearson Lachlan J, Rait Christopher, Nicholls M Gary, Yandle Timothy G, Evans John J
Department of Obstetrics and Gynaecology, Christchurch School of Medicine and Health Sciences, University of Otago, New Zealand.
J Endocrinol. 2006 Oct;191(1):171-7. doi: 10.1677/joe.1.06815.
It is well documented that there are gender differences in the incidence and patterns of cardiovascular diseases but the reasons are unclear. Sex steroids may modulate the behaviour of vascular endothelial cells, which in turn act by paracrine processes to alter adjacent vascular smooth muscle activity. We hypothesised that the sex steroids alter the percentage of vascular endothelial cells that secrete the vasodilator peptide, adrenomedullin and modify the adrenomedullin-stimulating action of angiotensin-II. The percentage of adrenomedullin-secreting human aortic endothelial cells was determined using the cell immunoblot method. Cells were incubated with selected concentrations of angiotensin-II, oestradiol and testosterone alone and sex steroids in combination with angiotensin-II. Adrenomedullin mRNA expression in endothelial cells was quantified by real-time PCR. It was observed that at 4 h, angiotensin-II increased the percentage of adrenomedullin-secreting cells in a concentration-dependent manner. Testosterone at physiological concentrations was observed to increase the number of adrenomedullin-secreting cells whilst oestradiol had no effect. Addition of testosterone to angiotensin-II resulted in less than additive increases in the number of cells secreting adrenomedullin. Oestradiol reduced the angiotensin-II-induced increase in adrenomedullin-secreting cells. Adrenomedullin mRNA expression was significantly increased by testosterone and there was also a trend for an increase in adrenomedullin mRNA expression, which occurred when cells were incubated with angiotensin-II. Our results point to a complex interplay between the sex steroids and angiotensin-II in regulating adrenomedullin production by human endothelial cells, which may contribute to gender-related differences in vascular disease in humans.
有充分的文献记载,心血管疾病的发病率和模式存在性别差异,但其原因尚不清楚。性类固醇可能调节血管内皮细胞的行为,而血管内皮细胞又通过旁分泌过程来改变相邻血管平滑肌的活性。我们假设性类固醇会改变分泌血管舒张肽肾上腺髓质素的血管内皮细胞的百分比,并改变血管紧张素-II对肾上腺髓质素的刺激作用。采用细胞免疫印迹法测定分泌肾上腺髓质素的人主动脉内皮细胞的百分比。将细胞分别与选定浓度的血管紧张素-II、雌二醇和睾酮单独孵育,以及将性类固醇与血管紧张素-II联合孵育。通过实时PCR对内皮细胞中肾上腺髓质素mRNA的表达进行定量。结果发现,在4小时时,血管紧张素-II以浓度依赖的方式增加了分泌肾上腺髓质素的细胞百分比。观察到生理浓度的睾酮会增加分泌肾上腺髓质素的细胞数量,而雌二醇则没有作用。在血管紧张素-II中添加睾酮导致分泌肾上腺髓质素的细胞数量增加小于相加效应。雌二醇减少了血管紧张素-II诱导的分泌肾上腺髓质素的细胞增加。睾酮显著增加了肾上腺髓质素mRNA的表达,并且当细胞与血管紧张素-II孵育时,肾上腺髓质素mRNA的表达也有增加的趋势。我们的结果表明,性类固醇和血管紧张素-II在调节人内皮细胞产生肾上腺髓质素方面存在复杂的相互作用,这可能导致人类血管疾病中与性别相关的差异。