Gupte Manisha, Boustany-Kari Carine M, Bharadwaj Kalyani, Police Sara, Thatcher Sean, Gong Ming C, English Victoria L, Cassis Lisa A
Graduate Center for Nutritional Sciences, Rm. 521b, Wethington Bldg., 900 S. Limestone, College of Medicine, Univ. of Kentucky, Lexington, KY 40536-0200, USA.
Am J Physiol Regul Integr Comp Physiol. 2008 Sep;295(3):R781-8. doi: 10.1152/ajpregu.00183.2008. Epub 2008 Jul 23.
Adipose tissue expresses components of the renin-angiotensin system (RAS). Angiotensin converting enzyme (ACE2), a new component of the RAS, catabolizes the vasoconstrictor peptide ANG II to form the vasodilator angiotensin 1-7 [ANG-(1-7)]. We examined whether adipocytes express ACE2 and its regulation by manipulation of the RAS and by high-fat (HF) feeding. ACE2 mRNA expression increased (threefold) during differentiation of 3T3-L1 adipocytes and was not regulated by manipulation of the RAS. Male C57BL/6 mice were fed low- (LF) or high-fat (HF) diets for 1 wk or 4 mo. At 1 wk of HF feeding, adipose expression of angiotensinogen (twofold) and ACE2 (threefold) increased, but systemic angiotensin peptide concentrations and blood pressure were not altered. At 4 mo of HF feeding, adipose mRNA expression of angiotensinogen (twofold) and ACE2 (threefold) continued to be elevated, and liver angiotensinogen expression increased (twofold). However, adipose tissue from HF mice did not exhibit elevated ACE2 protein or activity. Increased expression of ADAM17, a protease responsible for ACE2 shedding, coincided with reductions in ACE2 activity in 3T3-L1 adipocytes, and an ADAM17 inhibitor decreased media ACE2 activity. Moreover, ADAM17 mRNA expression was increased in adipose tissue from 4-mo HF-fed mice, and plasma ACE2 activity increased. However, HF mice exhibited marked increases in plasma angiotensin peptide concentrations (LF: 2,141 +/- 253; HF: 6,829 +/- 1,075 pg/ml) and elevated blood pressure. These results demonstrate that adipocytes express ACE2 that is dysregulated in HF-fed mice with elevated blood pressure compared with LF controls.
脂肪组织表达肾素-血管紧张素系统(RAS)的组分。血管紧张素转换酶(ACE2)是RAS的一个新组分,可将血管收缩肽ANG II分解代谢形成血管舒张肽血管紧张素1-7 [ANG-(1-7)]。我们研究了脂肪细胞是否表达ACE2,以及通过RAS调控和高脂(HF)喂养对其进行的调节。在3T3-L1脂肪细胞分化过程中,ACE2 mRNA表达增加(增至三倍),且不受RAS调控的影响。雄性C57BL/6小鼠分别喂食低脂肪(LF)或高脂肪(HF)饮食1周或4个月。在HF喂养1周时,脂肪组织中血管紧张素原(增至两倍)和ACE2(增至三倍)的表达增加,但全身血管紧张素肽浓度和血压未改变。在HF喂养4个月时,脂肪组织中血管紧张素原(增至两倍)和ACE2(增至三倍)的mRNA表达持续升高,肝脏血管紧张素原表达增加(增至两倍)。然而,HF小鼠的脂肪组织中ACE2蛋白或活性并未升高。负责ACE2脱落的蛋白酶ADAM17表达增加,与3T3-L1脂肪细胞中ACE2活性降低同时出现,且ADAM17抑制剂可降低培养基中ACE2活性。此外,4个月HF喂养小鼠的脂肪组织中ADAM17 mRNA表达增加,血浆ACE2活性升高。然而,HF小鼠的血浆血管紧张素肽浓度显著升高(LF:2,141±253;HF:6,829±1,075 pg/ml)且血压升高。这些结果表明,脂肪细胞表达ACE2,与LF对照组相比,在血压升高的HF喂养小鼠中ACE2表达失调。