NOX2 是血管紧张素 II 在致密斑诱导产生超氧阴离子的主要来源。
NOX2 is the primary source of angiotensin II-induced superoxide in the macula densa.
机构信息
Department of Physiology & Biophysics, University of Mississippi Medical Center, Jackson, MS 39216, USA.
出版信息
Am J Physiol Regul Integr Comp Physiol. 2010 Mar;298(3):R707-12. doi: 10.1152/ajpregu.00762.2009. Epub 2010 Jan 6.
Macula densa (MD)-mediated regulation of renal hemodynamics via tubuloglomerular feedback is regulated by interactions between factors such as superoxide (O(2)(-)) and angiotensin II (ANG II). We have reported that NaCl-induced O(2)(-) in the MD is produced by the NOX2 isoform of NADPH oxidase (NOX); however, the source of ANG II-induced O(2)(-) in MD is unknown. Thus we determined the pathways by which ANG II increased O(2)(-) in the MD by measuring O(2)(-) in ANG II-treated MMDD1 cells, a MD-like cell line. ANG II caused MMDD1 O(2)(-) levels to increase by more than twofold (P < 0.01). This increase was blocked by losartan (AT(1) receptor blocker) but not PD-123319 (AT(2) receptor antagonist). Apocynin (a NOX inhibitor) decreased O(2)(-) by 86% (P < 0.01), whereas oxypurinol (a xanthine oxidase inhibitor) and NS-398 (a cyclooxygenase-2 inhibitor) had no significant effect. The NOX-dependent increase in O(2)(-) was due to the NOX2 isoform; a short interfering (si)RNA against NOX2 blunted ANG II-induced increases in O(2)(-), whereas the NOX4/siRNA did not. Finally, we found that inhibiting the Rac1 subunit of NOX blunted ANG II-induced O(2)(-) production in NOX4/siRNA-treated cells but did not further decrease it in NOX2/siRNA-treated cells. Our results indicate that ANG II stimulates O(2)(-) production in the MD primarily via AT(1)-dependent activation of NOX2. Rac1 is required for the full activation of NOX2. This pathway may be an important component of ANG II enhancement of tubuloglomerular feedback.
致密斑(MD)通过管球反馈调节肾血流动力学的作用受到超氧化物(O(2)(-))和血管紧张素 II(ANG II)等因素相互作用的调节。我们已经报道过,MD 中的 NaCl 诱导的 O(2)(-)是由 NADPH 氧化酶(NOX)的 NOX2 同工型产生的;然而,MD 中 ANG II 诱导的 O(2)(-)的来源尚不清楚。因此,我们通过测量 MD 样细胞系 MMDD1 细胞中 ANG II 处理后的 O(2)(-)来确定 ANG II 增加 MD 中 O(2)(-)的途径。ANG II 使 MMDD1 的 O(2)(-)水平增加了两倍以上(P < 0.01)。这种增加被 losartan(AT(1)受体阻滞剂)阻断,但不受 PD-123319(AT(2)受体拮抗剂)的影响。Apocynin(NOX 抑制剂)使 O(2)(-)降低了 86%(P < 0.01),而 oxypurinol(黄嘌呤氧化酶抑制剂)和 NS-398(环氧化酶-2 抑制剂)则没有显著影响。NOX 依赖性的 O(2)(-)增加是由于 NOX2 同工型;针对 NOX2 的短干扰 (si)RNA 减弱了 ANG II 诱导的 O(2)(-)增加,而 NOX4/siRNA 则没有。最后,我们发现抑制 NOX 的 Rac1 亚基减弱了 NOX4/siRNA 处理细胞中 ANG II 诱导的 O(2)(-)产生,但在 NOX2/siRNA 处理细胞中进一步降低它并没有影响。我们的结果表明,ANG II 通过 AT(1)依赖性激活 NOX2 刺激 MD 中 O(2)(-)的产生。Rac1 是 NOX2 完全激活所必需的。该途径可能是 ANG II 增强管球反馈的重要组成部分。