Department of Neurology, Second Xiangya Hospital, Central South University, Changsha, Hunan 410011, P.R. China.
Int J Mol Med. 2021 Apr;47(4). doi: 10.3892/ijmm.2021.4871. Epub 2021 Feb 4.
The Golgi apparatus is known to underpin many important cellular homeostatic functions, including trafficking, sorting and modifications of proteins or lipids. These functions are dysregulated in neurodegenerative diseases, cancer, infectious diseases and cardiovascular diseases, and the number of disease‑related genes associated with Golgi apparatus is on the increase. Recently, many studies have suggested that the mutations in the genes encoding Golgi resident proteins can trigger the occurrence of diseases. By summarizing the pathogenesis of these genetic diseases, it was found that most of these diseases have defects in membrane trafficking. Such defects typically result in mislocalization of proteins, impaired glycosylation of proteins, and the accumulation of undegraded proteins. In the present review, we aim to understand the patterns of mutations in the genes encoding Golgi resident proteins and decipher the interplay between Golgi resident proteins and membrane trafficking pathway in cells. Furthermore, the detection of Golgi resident protein in human serum samples has the potential to be used as a diagnostic tool for diseases, and its central role in membrane trafficking pathways provides possible targets for disease therapy. Thus, we also introduced the clinical value of Golgi apparatus in the present review.
高尔基体被认为是许多重要的细胞内稳态功能的基础,包括蛋白质或脂质的运输、分拣和修饰。这些功能在神经退行性疾病、癌症、传染病和心血管疾病中失调,与高尔基体相关的疾病相关基因的数量正在增加。最近,许多研究表明,编码高尔基体驻留蛋白的基因突变可引发疾病的发生。通过总结这些遗传性疾病的发病机制,发现这些疾病大多存在膜运输缺陷。这种缺陷通常导致蛋白质定位错误、蛋白质糖基化受损以及未降解蛋白质的积累。在本综述中,我们旨在了解编码高尔基体驻留蛋白的基因突变模式,并解析高尔基体驻留蛋白与细胞内膜运输途径之间的相互作用。此外,高尔基体驻留蛋白在人血清样本中的检测有可能被用作疾病的诊断工具,其在膜运输途径中的核心作用为疾病治疗提供了可能的靶点。因此,我们也在本综述中介绍了高尔基体的临床价值。