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NGFI-B家族在肾上腺分区及肾上腺皮质疾病中的作用。

A role for the NGFI-B family in adrenal zonation and adrenocortical disease.

作者信息

Bassett Mary H, White Perrin C, Rainey William E

机构信息

Department of Obstetrics and Gynecology, Division of Reproductive Endocrinology University of Texas Southwestern Medical Center, Dallas, Texas 75390-9073, USA.

出版信息

Endocr Res. 2004 Nov;30(4):567-74. doi: 10.1081/erc-200043715.

Abstract

The three zones of the human adrenal cortex are functionally distinct with the glomerulosa producing aldosterone, the fasciculata producing cortisol, and the reticularis producing DHEA/DHEAS. This functional zonation is largely due to the zone-specific expression of steroidogenic enzymes. Recent evidence suggests a role for the NGFI-B family of orphan nuclear receptors (particularly NURR1 and NGFI-B) in the zone-specific expression of two key steroidogenic enzymes, aldosterone synthase (CYP11B2) and 3beta-hydroxysteroid dehydrogenase (HSD3B2). Herein we discuss the evidence that suggests a role for NURR1 (NR4A2) in the expression of CYP11B2 in the glomerulosa as well as in the dysregulation of CYP11B2 gene expression as is seen in aldosterone-producing adenoma (APA), a major cause of endocrine hypertension. NURR1 appears to be important for CYP11B2 transcription and is found at higher levels in glomerulosa and in APA. Its expression in adrenal cells is also readily increased by angiotensin II treatment. HSD3B2 is a steroid-metabolizing enzyme that is essential for adrenal production of mineralocorticoids and glucocorticoids. Thus, HSD3B2 is expressed at high levels in the glomerulosa and fasciculata where these steroids are produced but at low levels in the adrenal reticularis, which produces mainly DHEA. We recently demonstrated that NGFI-B (nur77 or NR4A1) plays an important role in the regulation of HSD3B2 transcription and may play an important role in the functional zonation of the adrenal gland. Immunohistochemistry confirmed that, within adult and fetal adrenal gland, NGFI-B expression paralleled expression of HSD3B2. Transient transfections demonstrated that NGFI-B family members enhanced HSD3B2 reporter activity but had no effect on a 17alpha-hydroxylase (CYP17) promoter construct. Taken together these results suggest that the NGFI-B family of transcription factors plays a role in establishing the functional zonation of the human adrenal by regulating CYP11B2 and HSD3B2 gene transcription.

摘要

人类肾上腺皮质的三个区域功能各异,球状带产生醛固酮,束状带产生皮质醇,网状带产生脱氢表雄酮/硫酸脱氢表雄酮。这种功能分区很大程度上归因于类固醇生成酶的区域特异性表达。最近的证据表明,孤儿核受体的NGFI - B家族(特别是NURR1和NGFI - B)在两种关键类固醇生成酶醛固酮合酶(CYP11B2)和3β - 羟基类固醇脱氢酶(HSD3B2)的区域特异性表达中发挥作用。在此我们讨论表明NURR1(NR4A2)在球状带CYP11B2表达中以及在醛固酮瘤(APA,内分泌性高血压的主要原因)中所见的CYP11B2基因表达失调中发挥作用的证据。NURR1似乎对CYP11B2转录很重要,并且在球状带和醛固酮瘤中水平较高。用血管紧张素II处理也可使肾上腺细胞中其表达容易增加。HSD3B2是一种类固醇代谢酶,对肾上腺产生盐皮质激素和糖皮质激素至关重要。因此,HSD3B2在产生这些类固醇的球状带和束状带中高水平表达,但在主要产生脱氢表雄酮(DHEA)的肾上腺网状带中低水平表达。我们最近证明,NGFI - B(nur77或NR4A1)在HSD3B2转录调控中起重要作用,并且可能在肾上腺的功能分区中起重要作用。免疫组织化学证实,在成年和胎儿肾上腺内,NGFI - B表达与HSD3B2表达平行。瞬时转染表明,NGFI - B家族成员增强HSD3B2报告基因活性,但对17α - 羟化酶(CYP17)启动子构建体无影响。这些结果综合起来表明,转录因子的NGFI - B家族通过调节CYP11B2和HSD3B2基因转录在建立人类肾上腺的功能分区中发挥作用。

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