神经周围网
硫酸化
神经科学
聚糖
痴呆
硫酸软骨素
神经认知
疾病
认知
化学
心理学
糖胺聚糖
生物化学
医学
病理
中枢神经系统
糖蛋白
作者
Aric F. Logsdon,Kendra Francis,Nicole E. Richardson,Shannon J. Hu,Chelsea L. Faber,Bao Anh Phan,Vy Nguyen,Naly Setthavongsack,William A. Banks,Randy Woltjer,C. Dirk Keene,Caitlin S. Latimer,Michael W. Schwartz,Jarrad M. Scarlett,Kimberly M. Alonge
摘要
Abstract The extracellular matrix (ECM) of the brain comprises unique glycan “sulfation codes” that influence neurological function. Perineuronal nets (PNNs) are chondroitin sulfate‐glycosaminoglycan (CS‐GAG) containing matrices that enmesh neural networks involved in memory and cognition, and loss of PNN matrices is reported in patients with neurocognitive and neuropsychiatric disorders including Alzheimer's disease (AD). Using liquid chromatography tandem mass spectrometry (LC‐MS/MS), we show that patients with a clinical diagnosis of AD‐related dementia undergo a re‐coding of their PNN‐associated CS‐GAGs that correlates to Braak stage progression, hyperphosphorylated tau (p‐tau) accumulation, and cognitive impairment. As these CS‐GAG sulfation changes are detectable prior to the regional onset of classical AD pathology, they may contribute to the initiation and/or progression of the underlying degenerative processes and implicate the brain matrix sulfation code as a key player in the development of AD clinicopathology.
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