Laboratory of Neurobiology, Neurology IX Unit, Fondazione IRCCS Istituto Neurologico Carlo Besta, 20133 Milan, Italy.
Cerebrovascular Unit, Fondazione IRCCS Istituto Neurologico Carlo Besta, 20133 Milan, Italy.
Int J Mol Sci. 2022 Apr 19;23(9):4492. doi: 10.3390/ijms23094492.
Ring Finger Protein 213 (RNF213), also known as Mysterin, is the major susceptibility factor for Moyamoya Arteriopathy (MA), a progressive cerebrovascular disorder that often leads to brain stroke in adults and children. Although several rare RNF213 polymorphisms have been reported, no major susceptibility variant has been identified to date in Caucasian patients, thus frustrating the attempts to identify putative therapeutic targets for MA treatment. For these reasons, the investigation of novel biochemical functions, substrates and unknown partners of RNF213 will help to unravel the pathogenic mechanisms of MA and will facilitate variant interpretations in a diagnostic context in the future. The aim of the present review is to discuss novel perspectives regarding emerging RNF213 roles in light of recent literature updates and dissect their relevance for understanding MA and for the design of future research studies. Since its identification, RNF213 involvement in angiogenesis and vasculogenesis has strengthened, together with its role in inflammatory signals and proliferation pathways. Most recent studies have been increasingly focused on its relevance in antimicrobial activity and lipid metabolism, highlighting new intriguing perspectives. The last area could suggest the main role of RNF213 in the proteasome pathway, thus reinforcing the hypotheses already previously formulated that depict the protein as an important regulator of the stability of client proteins involved in angiogenesis. We believe that the novel evidence reviewed here may contribute to untangling the complex and still obscure pathogenesis of MA that is reflected in the lack of therapies able to slow down or halt disease progression and severity.
环指蛋白 213(RNF213),又称为 Mysterin,是烟雾病(MA)的主要易感因素,MA 是一种进行性脑血管疾病,常导致成人和儿童中风。尽管已经报道了几种罕见的 RNF213 多态性,但迄今为止,在白种人群体中尚未发现主要的易感变异体,这使得寻找 MA 治疗的潜在治疗靶点的尝试受挫。出于这些原因,研究 RNF213 的新生化功能、底物和未知伴侣将有助于揭示 MA 的发病机制,并有助于在未来的诊断背景下解释变异体。本综述的目的是讨论 RNF213 在新兴作用方面的新观点,鉴于最近的文献更新,并剖析它们对理解 MA 和设计未来研究的相关性。自鉴定以来,RNF213 参与血管生成和血管发生的作用得到了加强,同时它在炎症信号和增殖途径中的作用也得到了加强。最近的研究越来越关注其在抗菌活性和脂质代谢中的相关性,突出了新的有趣观点。最后一个领域可能表明 RNF213 在蛋白酶体途径中的主要作用,从而加强了先前已经提出的假设,即该蛋白是参与血管生成的客户蛋白稳定性的重要调节剂。我们相信,这里综述的新证据可能有助于阐明 MA 复杂而仍不清楚的发病机制,这种机制反映在缺乏能够减缓或阻止疾病进展和严重程度的治疗方法上。