University of Texas at Austin, Marine Science Institute, Port Aransas, 78373, USA.
Am J Physiol Endocrinol Metab. 2011 Oct;301(4):E637-48. doi: 10.1152/ajpendo.00168.2011. Epub 2011 Jul 5.
Insulin-like growth factor-binding proteins (IGFBPs) play important roles in downregulating IGF activity and growth and development in vertebrates under hypoxic stress. However, the mechanisms of hypoxia regulation of IGFBPs in teleost fishes are unknown. The involvement of reactive oxygen species (ROS) and hypoxia-inducible factors (HIFs) in hypoxia upregulation of IGFBPs in Atlantic croaker were investigated. Three croaker IGFBPs, IGFBP-1, IGFBP-2, and IGFBP-5, were cloned and characterized. Chronic hypoxia exposure [dissolved oxygen (DO): 1.7 mg/l for 2-4 wk] caused significant increases in hepatic and neural IGFBP-1 mRNA expression compared with tissue mRNA levels in fish held under normoxic conditions (6.5 mg DO/l). Moreover, longer-term chronic hypoxia exposure (2-2.7 mg DO/l for 15-20 wk) caused significant increases in mRNA levels of all three IGFBPs in both liver and brain tissues. Hypoxia exposure also markedly increased superoxide radical (O(2)(·-), an index of ROS) production and HIF-1α mRNA and HIF-2α protein expression in croaker livers. Pharmacological treatment with an antioxidant attenuated the hypoxia-induced increases in O(2)(·-) production and HIFα mRNA and protein expression as well as the elevation of IGFBP-1 mRNA levels. These results suggest that the upregulation of IGFBP expression under hypoxia stress is due, in part, to alterations in the antioxidant status, which may involve ROS and HIFs.
胰岛素样生长因子结合蛋白(IGFBPs)在脊椎动物缺氧应激下通过下调 IGF 活性和生长发育起着重要作用。然而,鱼类 IGFBPs 受缺氧调控的机制尚不清楚。本研究探讨了活性氧(ROS)和缺氧诱导因子(HIFs)在褐牙鲆 IGFBPs 缺氧上调中的作用。克隆和鉴定了三种褐牙鲆 IGFBPs,IGFBP-1、IGFBP-2 和 IGFBP-5。慢性缺氧暴露[溶解氧(DO):1.7 mg/l 持续 2-4 周]导致与正常氧条件(6.5 mg DO/l)下鱼类组织 mRNA 水平相比,肝脏和神经 IGFBP-1 mRNA 表达显著增加。此外,长期慢性缺氧暴露(2-2.7 mg DO/l 持续 15-20 周)导致肝脏和脑组织中所有三种 IGFBPs 的 mRNA 水平均显著增加。缺氧暴露还显著增加了褐牙鲆肝脏中超氧自由基(O2(·-),ROS 的一个指标)的产生以及 HIF-1α mRNA 和 HIF-2α 蛋白的表达。抗氧化剂的药理学处理减弱了缺氧诱导的 O2(·-)产生以及 HIFα mRNA 和蛋白表达和 IGFBP-1 mRNA 水平的升高。这些结果表明,缺氧应激下 IGFBP 表达的上调部分归因于抗氧化状态的改变,这可能涉及 ROS 和 HIFs。