Biological Sciences, University of Southampton, Southampton, United Kingdom.
Front Immunol. 2018 May 15;9:1024. doi: 10.3389/fimmu.2018.01024. eCollection 2018.
Optineurin is a multifunctional adaptor protein intimately involved in various vesicular trafficking pathways. Through interactions with an array of proteins, such as myosin VI, huntingtin, Rab8, and Tank-binding kinase 1, as well as via its oligomerisation, optineurin has the ability to act as an adaptor, scaffold, or signal regulator to coordinate many cellular processes associated with the trafficking of membrane-delivered cargo. Due to its diverse interactions and its distinct functions, optineurin is an essential component in a number of homeostatic pathways, such as protein trafficking and organelle maintenance. Through the binding of polyubiquitinated cargoes via its ubiquitin-binding domain, optineurin also serves as a selective autophagic receptor for the removal of a wide range of substrates. Alternatively, it can act in an ubiquitin-independent manner to mediate the clearance of protein aggregates. Regarding its disease associations, mutations in the optineurin gene are associated with glaucoma and have more recently been found to correlate with Paget's disease of bone and amyotrophic lateral sclerosis (ALS). Indeed, ALS-associated mutations in optineurin result in defects in neuronal vesicular localisation, autophagosome-lysosome fusion, and secretory pathway function. More recent molecular and functional analysis has shown that it also plays a role in mitophagy, thus linking it to a number of other neurodegenerative conditions, such as Parkinson's. Here, we review the role of optineurin in intracellular membrane trafficking, with a focus on autophagy, and describe how upstream signalling cascades are critical to its regulation. Current data and contradicting reports would suggest that optineurin is an important and selective autophagy receptor under specific conditions, whereby interplay, synergy, and functional redundancy with other receptors occurs. We will also discuss how dysfunction in optineurin-mediated pathways may lead to perturbation of critical cellular processes, which can drive the pathologies of number of diseases. Therefore, further understanding of optineurin function, its target specificity, and its mechanism of action will be critical in fully delineating its role in human disease.
视神经病变蛋白是一种多功能衔接蛋白,密切参与各种小泡运输途径。通过与肌球蛋白 VI、亨廷顿蛋白、Rab8 和 Tank 结合激酶 1 等一系列蛋白相互作用,以及通过其寡聚化,视神经病变蛋白能够作为衔接蛋白、支架或信号调节剂,协调与膜递货运送相关的许多细胞过程。由于其多样化的相互作用及其独特的功能,视神经病变蛋白是许多内稳态途径(如蛋白质运输和细胞器维持)的重要组成部分。通过其泛素结合结构域与多泛素化货物结合,视神经病变蛋白也作为多种底物清除的选择性自噬受体。或者,它可以以非泛素依赖的方式发挥作用,介导蛋白聚集体的清除。关于其与疾病的关联,视神经病变蛋白基因的突变与青光眼有关,最近还发现与 Pagets 病和肌萎缩侧索硬化症(ALS)相关。事实上,视神经病变蛋白中的 ALS 相关突变导致神经元小泡定位、自噬体-溶酶体融合和分泌途径功能缺陷。最近的分子和功能分析表明,它还在细胞自噬中发挥作用,从而与许多其他神经退行性疾病(如帕金森病)相关。在这里,我们综述了视神经病变蛋白在细胞内膜运输中的作用,重点介绍了自噬,并描述了上游信号级联对其调节的重要性。目前的数据和相互矛盾的报告表明,在特定条件下,视神经病变蛋白是一种重要的和选择性的自噬受体,在此过程中,它与其他受体相互作用、协同和功能冗余。我们还将讨论视神经病变蛋白介导的途径功能障碍如何导致关键细胞过程的紊乱,从而引发多种疾病的病理。因此,进一步了解视神经病变蛋白的功能、其靶标特异性及其作用机制,对于充分阐明其在人类疾病中的作用至关重要。