Department of Physiology, McGill University, Montreal, HG3 1Y6, Canada.
Quantitative Life Sciences Program, McGill University, Montreal, Canada.
Mol Neurodegener. 2023 Aug 7;18(1):52. doi: 10.1186/s13024-023-00639-y.
The AAA ATPase valosin containing protein (VCP) is essential for cell and organ homeostasis, especially in cells of the nervous system. As part of a large network, VCP collaborates with many cofactors to ensure proteostasis under normal, stress, and disease conditions. A large number of mutations have revealed the importance of VCP for human health. In particular, VCP facilitates the dismantling of protein aggregates and the removal of dysfunctional organelles. These are critical events to prevent malfunction of the brain and other parts of the nervous system. In line with this idea, VCP mutants are linked to the onset and progression of neurodegeneration and other diseases. The intricate molecular mechanisms that connect VCP mutations to distinct brain pathologies continue to be uncovered. Emerging evidence supports the model that VCP controls cellular functions on multiple levels and in a cell type specific fashion. Accordingly, VCP mutants derail cellular homeostasis through several mechanisms that can instigate disease. Our review focuses on the association between VCP malfunction and neurodegeneration. We discuss the latest insights in the field, emphasize open questions, and speculate on the potential of VCP as a drug target for some of the most devastating forms of neurodegeneration.
AAA ATP 酶包含素蛋白 (VCP) 是细胞和器官稳态的必需物质,尤其是在神经系统细胞中。作为一个大型网络的一部分,VCP 与许多辅助因子合作,以确保在正常、应激和疾病条件下的蛋白质稳态。大量的突变揭示了 VCP 对人类健康的重要性。特别是,VCP 有助于分解蛋白质聚集体和去除功能失调的细胞器。这些是防止大脑和神经系统其他部位功能失调的关键事件。与这一观点一致,VCP 突变与神经退行性变和其他疾病的发生和进展有关。将 VCP 突变与特定的脑病理学联系起来的复杂分子机制仍在不断被揭示。新出现的证据支持 VCP 在多个层面上以细胞类型特异性的方式控制细胞功能的模型。因此,VCP 突变通过几种机制破坏细胞内稳态,从而引发疾病。我们的综述重点关注 VCP 功能障碍与神经退行性变之间的关联。我们讨论了该领域的最新见解,强调了未解决的问题,并推测 VCP 作为一些最具破坏性的神经退行性变形式的药物靶点的潜力。