Center for Integrative Genomics Faculty of Biology and Medicine University of Lausanne Switzerland.
Department of Medical Sciences University of Trieste Italy.
FEBS Open Bio. 2019 Jan 18;9(2):328-334. doi: 10.1002/2211-5463.12579. eCollection 2019 Feb.
Obesity is a condition characterized by adipose tissue hypertrophy; it is estimated that the obesity epidemic accounted for 4 million deaths in 2015 and that 70% of these were due to cardiovascular disease (CVD). One of the mechanisms linking obesity to CVD is the ability of adipose tissue to secrete circulating factors. We hypothesized that adipose tissue and its secretory products may influence mineralocorticoid receptor (MR) expression. Here, we showed that expression of MR and its downstream targets (, , and ) were significantly reduced in the kidneys of peroxisome proliferator-activated receptor-γ null ( ) and A-ZIP/F-1 (AZIP) lipoatrophic mice with respect to their controls. Intriguingly, MR expression was also found to be significantly reduced in the kidneys of genetically obese ob/ob mice. Our data suggest that adipose tissue contributes to the regulation of MR expression. Given that leptin deficiency seems to be the major feature shared by , AZIP, and ob/ob mice, we speculate that adipose tissue modulates MR expression through the leptin system.
肥胖症是一种以脂肪组织肥大为特征的病症;据估计,2015 年肥胖症流行导致 400 万人死亡,其中 70%归因于心血管疾病(CVD)。将肥胖与 CVD 联系起来的机制之一是脂肪组织分泌循环因子的能力。我们假设脂肪组织及其分泌产物可能会影响盐皮质激素受体(MR)的表达。在这里,我们发现过氧化物酶体增殖物激活受体-γ 缺失()和 A-ZIP/F-1(AZIP)脂肪营养不良小鼠的肾脏中,MR 及其下游靶标(、和)的表达相对于其对照明显降低。有趣的是,肥胖基因 ob/ob 小鼠的肾脏中也发现 MR 表达明显降低。我们的数据表明,脂肪组织有助于调节 MR 的表达。鉴于瘦素缺乏似乎是、AZIP 和 ob/ob 小鼠的主要共同特征,我们推测脂肪组织通过瘦素系统调节 MR 表达。