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四跨膜蛋白12(TSPAN12)是肾上腺生理和醛固酮分泌性腺瘤中醛固酮生成的新型负调节因子。

TSPAN12 (Tetraspanin 12) Is a Novel Negative Regulator of Aldosterone Production in Adrenal Physiology and Aldosterone-Producing Adenomas.

作者信息

Gong Siyuan, Tetti Martina, Kemter Elisabeth, Peitzsch Mirko, Mulatero Paolo, Bidlingmaier Martin, Eisenhofer Graeme, Wolf Eckhard, Reincke Martin, Williams Tracy Ann

机构信息

Medizinische Klinik und Poliklinik IV, Klinikum der Universität München, LMU München, Germany (S.G., M.T., M.B., M.R., T.A.W.).

Division of Internal Medicine and Hypertension, Department of Medical Sciences, University of Turin, Italy (M.T., P.M., T.A.W.).

出版信息

Hypertension. 2023 Feb;80(2):440-450. doi: 10.1161/HYPERTENSIONAHA.122.19783. Epub 2022 Dec 2.

Abstract

BACKGROUND

Aldosterone-producing adenomas (APAs) are a major cause of primary aldosteronism, a condition of low-renin hypertension, in which aldosterone overproduction is usually driven by a somatic activating mutation in an ion pump or channel. is differentially expressed in different subgroups of APAs suggesting a role in APA pathophysiology. Our objective was to determine the function of TSPAN12 (tetraspanin 12) in adrenal physiology and pathophysiology.

METHODS

APA specimens, pig adrenals under dietary sodium modulation, and a human adrenocortical cell line HAC15 were used for functional characterization of TSPAN12 in vivo and in vitro.

RESULTS

Gene ontology analysis of 21 APA transcriptomes dichotomized according to high versus low transcript levels highlighted a function for related to the renin-angiotensin system. expression levels in a cohort of 30 APAs were inversely correlated with baseline plasma aldosterone concentrations (=-0.47; =0.009). In a pig model of renin-angiotensin system activation by dietary salt restriction, mRNA levels and TSPAN12 immunostaining were markedly increased in the zona glomerulosa layer of the adrenal cortex. In vitro stimulation of human adrenocortical human adrenocortical cells with 10 nM angiotensin II for 6 hours caused a 1.6-fold±0.13 increase in expression, which was ablated by 10 μM nifedipine (=0.0097) or 30 μM W-7 (=0.0022). Gene silencing of in human adrenocortical cells demonstrated its inverse effect on aldosterone secretion under basal and angiotensin II stimulated conditions.

CONCLUSIONS

Our findings show that TSPAN12 is a negative regulator of aldosterone production and could contribute to aldosterone overproduction in primary aldosteronism.

摘要

背景

醛固酮瘤(APA)是原发性醛固酮增多症(一种低肾素性高血压疾病)的主要病因,其中醛固酮的过度产生通常由离子泵或通道中的体细胞激活突变驱动。在不同亚组的APA中差异表达,提示其在APA病理生理学中发挥作用。我们的目的是确定四跨膜蛋白12(TSPAN12)在肾上腺生理和病理生理中的功能。

方法

使用APA标本、饮食钠调节下的猪肾上腺以及人肾上腺皮质细胞系HAC15对TSPAN12进行体内和体外功能表征。

结果

根据转录水平高低对21个APA转录组进行二分法基因本体分析,突出了与肾素-血管紧张素系统相关的功能。30个APA队列中的表达水平与基线血浆醛固酮浓度呈负相关(r=-0.47;P=0.009)。在通过饮食盐限制激活肾素-血管紧张素系统的猪模型中,肾上腺皮质球状带层的mRNA水平和TSPAN12免疫染色显著增加。用人肾上腺皮质细胞系HAC15进行体外实验,用10 nM血管紧张素II刺激6小时,导致表达增加1.6倍±0.13,这被10 μM硝苯地平(P=0.0097)或30 μM W-7(P=0.0022)消除。在人肾上腺皮质细胞中对进行基因沉默,结果表明其在基础和血管紧张素II刺激条件下对醛固酮分泌具有相反作用。

结论

我们的研究结果表明,TSPAN12是醛固酮产生的负调节因子,可能在原发性醛固酮增多症中导致醛固酮过度产生。

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