Instituto de Biofísica Carlos Chagas Filho, Universidade Federal do Rio de Janeiro, Cidade Universitária, Rio de Janeiro, RJ, Brazil.
Am J Physiol Endocrinol Metab. 2012 Sep 15;303(6):E787-97. doi: 10.1152/ajpendo.00223.2012. Epub 2012 Jul 24.
α-Class GST (Gsta) represents an essential component of cellular antioxidant defense mechanisms in both the liver and the kidney. Estrogens and thyroid hormones (TH) play central roles in animal development, physiology, and behavior. Evidence of the overlapping functions of thyroid hormones and estrogens has been shown, although the molecular mechanisms are not always clear. We evaluated an interaction between TH and estradiol in regulating kidney Gsta expression and function. First, we observed that female mice expressed greater amounts of Gsta compared with males and showed an opposite pattern of expression in TRβ knock-in mice. To further investigate these sex differences, hypothyroidism was induced by a 5-propyl-2-thiouracil diet, and hyperthyroidism was induced by daily T₃ injections. Hypothyroidism increased kidney Gsta expression in male mice but not in female mice, indicating that sex hormones could be influencing the regulation of Gsta by thyroid hormones. To analyze this hypothesis, ovariectomized females were subjected to hypo- and hyperthyroidism, which led to a male profile of Gsta expression. When hypo- or hyperthyroid ovariectomized mice were treated with 17β-estradiol benzoate, we were able to confirm that estradiol was interfering with TH modulation; Gsta expression is increased by T₃ when estradiol is present and decreased by T₃ when estradiol is absent. Using proximal tubule cells, we also showed that estradiol and T₃ worked together to modulate Gsta expression in an overlapping fashion. In summary, 1) the sex difference in the basal expression of Gsta impacts the detoxification process, 2) kidney Gsta expression is regulated by TH in males and females but in opposite directions, and 3) T₃ and estradiol interact directly in renal proximal cells to regulate Gsta expression in females.
α 类 GST(Gsta)是肝脏和肾脏细胞抗氧化防御机制的重要组成部分。雌激素和甲状腺激素(TH)在动物的发育、生理和行为中起着核心作用。尽管分子机制并不总是清楚,但已经有证据表明甲状腺激素和雌激素的功能有重叠。我们评估了 TH 和雌二醇在调节肾脏 Gsta 表达和功能方面的相互作用。首先,我们观察到雌性小鼠比雄性小鼠表达更多的 Gsta,并在 TRβ 敲入小鼠中表现出相反的表达模式。为了进一步研究这些性别差异,我们通过 5-丙基-2-硫尿嘧啶饮食诱导甲状腺功能减退症,通过每天注射 T₃ 诱导甲状腺功能亢进症。甲状腺功能减退症增加了雄性小鼠肾脏 Gsta 的表达,但不增加雌性小鼠肾脏 Gsta 的表达,这表明性激素可能影响甲状腺激素对 Gsta 的调节。为了分析这一假设,我们对去卵巢雌性小鼠进行了甲状腺功能减退症和甲状腺功能亢进症的诱导,这导致了 Gsta 表达的雄性模式。当去卵巢的甲状腺功能减退症或甲状腺功能亢进症的雌性小鼠接受 17β-雌二醇苯甲酸酯治疗时,我们能够证实雌二醇干扰了 TH 的调节;当存在雌二醇时,T₃ 增加 Gsta 的表达,当不存在雌二醇时,T₃ 降低 Gsta 的表达。使用近端肾小管细胞,我们还表明,雌二醇和 T₃ 以重叠的方式共同调节 Gsta 的表达。总之,1)Gsta 基础表达的性别差异影响解毒过程,2)TH 在雄性和雌性中调节肾脏 Gsta 的表达,但方向相反,3)T₃ 和雌二醇在肾脏近端细胞中直接相互作用,调节雌性 Gsta 的表达。