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Sirtuin 3 缺乏不会增强低氧诱导的肺动脉高压。

Sirtuin 3 deficiency does not augment hypoxia-induced pulmonary hypertension.

机构信息

Department of Pediatrics, Division of Neonatology 1 , Northwestern University Feinberg School of Medicine, Chicago, Illinois; and.

出版信息

Am J Respir Cell Mol Biol. 2013 Dec;49(6):885-91. doi: 10.1165/rcmb.2013-0191OC.

Abstract

Alveolar hypoxia elicits increases in mitochondrial reactive oxygen species (ROS) signaling in pulmonary arterial (PA) smooth muscle cells (PASMCs), triggering hypoxic pulmonary vasoconstriction. Mice deficient in sirtuin (Sirt) 3, a nicotinamide adenine dinucleotide-dependent mitochondrial deacetylase, demonstrate enhanced left ventricular hypertrophy after aortic banding, whereas cells from these mice reportedly exhibit augmented hypoxia-induced ROS signaling and hypoxia-inducible factor (HIF)-1 activation. We therefore tested whether deletion of Sirt3 would augment hypoxia-induced ROS signaling in PASMCs, thereby exacerbating the development of pulmonary hypertension (PH) and right ventricular hypertrophy. In PASMCs from Sirt3 knockout (Sirt3(-/-)) mice in the C57BL/6 background, we observed that acute hypoxia (1.5% O2; 30 min)-induced changes in ROS signaling, detected using targeted redox-sensitive, ratiometric fluorescent protein sensors (roGFP) in the mitochondrial matrix, intermembrane space, and the cytosol, were indistinguishable from Sirt3(+/+) cells. Acute hypoxia-induced cytosolic calcium signaling in Sirt3(-/-) PASMCs was also indistinguishable from Sirt3(+/+) cells. During sustained hypoxia (1.5% O2; 16 h), Sirt3 deletion augmented mitochondrial matrix oxidant stress, but this did not correspond to an augmentation of intermembrane space or cytosolic oxidant signaling. Sirt3 deletion did not affect HIF-1α stabilization under normoxia, nor did it augment HIF-1α stabilization during sustained hypoxia (1.5% O2; 4 h). Sirt3(-/-) mice housed in chronic hypoxia (10% O2; 30 d) developed PH, PA wall remodeling, and right ventricular hypertrophy that was indistinguishable from Sirt3(+/+) littermates. Thus, Sirt3 deletion does not augment hypoxia-induced ROS signaling or its consequences in the cytosol of PASMCs, or the development of PH. These findings suggest that Sirt3 responses may be cell type specific, or restricted to certain genetic backgrounds.

摘要

肺泡缺氧会引起肺小动脉平滑肌细胞(PASMC)中线粒体活性氧物质(ROS)信号的增加,从而触发低氧性肺血管收缩。缺乏烟酰胺腺嘌呤二核苷酸依赖性线粒体去乙酰化酶 Sirtuin(Sirt)3 的小鼠在主动脉缩窄后表现出左心室肥厚增加,而这些小鼠的细胞据称表现出增强的缺氧诱导的 ROS 信号和缺氧诱导因子(HIF)-1 激活。因此,我们测试了 Sirt3 的缺失是否会增强 PASMC 中的缺氧诱导的 ROS 信号,从而加剧肺动脉高压(PH)和右心室肥厚的发展。在 C57BL/6 背景下 Sirt3 基因敲除(Sirt3(-/-))小鼠的 PASMC 中,我们观察到急性缺氧(1.5% O2;30 min)诱导的 ROS 信号变化,使用靶向氧化还原敏感的,比率荧光蛋白传感器(roGFP)在线粒体基质、内膜间隙和细胞质中检测到,与 Sirt3(+/+)细胞没有区别。急性缺氧诱导的 Sirt3(-/-)PASMC 中的细胞质钙信号也与 Sirt3(+/+)细胞没有区别。在持续缺氧(1.5% O2;16 h)期间,Sirt3 缺失增强了线粒体基质氧化剂应激,但这与内膜间隙或细胞质氧化剂信号的增强无关。Sirt3 缺失在常氧条件下不影响 HIF-1α的稳定,也不增强持续缺氧(1.5% O2;4 h)期间 HIF-1α的稳定。在慢性缺氧(10% O2;30 d)中饲养的 Sirt3(-/-)小鼠发展为 PH、PA 壁重塑和右心室肥厚,与 Sirt3(+/+)同窝仔鼠没有区别。因此,Sirt3 缺失不会增强 PASMC 细胞质中的缺氧诱导的 ROS 信号或其后果,也不会促进 PH 的发展。这些发现表明,Sirt3 反应可能是细胞类型特异性的,或者仅限于某些遗传背景。

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