Matsui Yusuke, Togayachi Akira, Sakamoto Kazuma, Angata Kiyohiko, Kadomatsu Kenji, Nishihara Shoko
Institute for Glyco-core Research (iGCORE), Nagoya University, Furo-cho, Chikusa-ku, Nagoya 464-8601, Japan.
Biomedical and Health Informatics Unit, Department of Integrated Health Science, Nagoya University Graduate School of Medicine, Daiko-minami, Higashi-ku, Nagoya, 461-8673, Japan.
bioRxiv. 2024 May 30:2023.12.25.573290. doi: 10.1101/2023.12.25.573290.
Glycosylation is increasingly recognized as a potential therapeutic target in Alzheimer's disease. In recent years, evidence of Alzheimer's disease-specific glycoproteins has been established. However, the mechanisms underlying their dysregulation, including tissue- and cell-type specificity, are not fully understood. We aimed to explore the upstream regulators of aberrant glycosylation by integrating multiple data sources using a glycogenomics approach. We identified dysregulation of the glycosyltransferase PLOD3 in oligodendrocytes as an upstream regulator of cerebral vessels and found that it is involved in COL4A5 synthesis, which is strongly correlated with amyloid fiber formation. Furthermore, COL4A5 has been suggested to interact with astrocytes via extracellular matrix receptors as a ligand. This study suggests directions for new therapeutic strategies for Alzheimer's disease targeting glycosyltransferases.
糖基化越来越被认为是阿尔茨海默病潜在的治疗靶点。近年来,已证实存在阿尔茨海默病特异性糖蛋白。然而,其失调的潜在机制,包括组织和细胞类型特异性,尚未完全明确。我们旨在通过糖原组学方法整合多个数据源来探索异常糖基化的上游调节因子。我们发现少突胶质细胞中糖基转移酶PLOD3的失调是脑血管的上游调节因子,并发现它参与了与淀粉样纤维形成密切相关的COL4A5的合成。此外,有研究表明COL4A5可作为配体通过细胞外基质受体与星形胶质细胞相互作用。本研究为针对糖基转移酶的阿尔茨海默病新治疗策略提供了方向。