Department of Biochemistry and Genetics, University of Navarra, 31008, Pamplona, Spain.
Navarra Institute for Health Research (IdiSNA), 31008, Pamplona, Spain.
J Physiol Biochem. 2023 May;79(2):383-395. doi: 10.1007/s13105-023-00955-3. Epub 2023 Mar 11.
NOX5 is the last member of the NADPH oxidase (NOXs) family to be identified and presents some specific characteristics differing from the rest of the NOXs. It contains four Ca binding domains at the N-terminus and its activity is regulated by the intracellular concentration of Ca. NOX5 generates superoxide (O) using NADPH as a substrate, and it modulates functions related to processes in which reactive oxygen species (ROS) are involved. Those functions appear to be detrimental or beneficial depending on the level of ROS produced. For example, the increase in NOX5 activity is related to the development of various oxidative stress-related pathologies such as cancer, cardiovascular, and renal diseases. In this context, pancreatic expression of NOX5 can negatively alter insulin action in high-fat diet-fed transgenic mice. This is consistent with the idea that the expression of NOX5 tends to increase in response to a stimulus or a stressful situation, generally causing a worsening of the pathology. On the other hand, it has also been suggested that it might have a positive role in preparing the body for metabolic stress, for example, by inducing a protective adipose tissue adaptation to the excess of nutrients supplied by a high-fat diet. In this line, its endothelial overexpression can delay lipid accumulation and insulin resistance development in obese transgenic mice by inducing the secretion of IL-6 followed by the expression of thermogenic and lipolytic genes. However, as NOX5 gene is not present in rodents and human NOX5 protein has not been crystallized, its function is still poorly characterized and further extensive research is required.
NOX5 是 NADPH 氧化酶 (NOXs) 家族中最后一个被鉴定的成员,具有一些与其他 NOXs 不同的特定特征。它在 N 端含有四个 Ca 结合结构域,其活性受细胞内 Ca 浓度的调节。NOX5 使用 NADPH 作为底物产生超氧阴离子 (O),并调节与活性氧 (ROS) 参与的过程相关的功能。这些功能似乎取决于产生的 ROS 水平而有益或有害。例如,NOX5 活性的增加与各种与氧化应激相关的病理学的发展有关,如癌症、心血管和肾脏疾病。在这种情况下,胰腺中 NOX5 的表达可以在高脂肪饮食喂养的转基因小鼠中负性改变胰岛素的作用。这与 NOX5 的表达倾向于响应刺激或应激情况而增加的观点一致,通常会导致病理学恶化。另一方面,也有人认为它可能在为代谢应激做准备方面发挥积极作用,例如通过诱导脂肪组织对高脂肪饮食提供的过量营养物质的适应性保护作用。在这方面,其内皮过表达可以通过诱导 IL-6 的分泌,随后表达生热和脂解基因,延迟肥胖转基因小鼠中的脂质积累和胰岛素抵抗的发展。然而,由于 NOX5 基因不存在于啮齿动物中,并且人类 NOX5 蛋白尚未结晶,因此其功能仍未得到充分表征,需要进一步广泛的研究。