Cell Growth, Tissue Repair and Regeneration (CRRET), UPEC EA 4397/ERL CNRS 9215, Université Paris Est Créteil, Université Paris Est, Créteil, France.
Aging and Neurodegenerative Diseases Brain Bank Investigation Laboratory, Universidade Federal de São Paulo, São Paulo, Brazil.
PLoS One. 2019 Jan 4;14(1):e0209573. doi: 10.1371/journal.pone.0209573. eCollection 2019.
Glycosaminoglycans (GAGs), including heparan sulfates and chondroitin sulfates, are major components of the extracellular matrix. Upon interacting with heparin binding growth factors (HBGF), GAGs participate to the maintaintenance of tissue homeostasis and contribute to self-healing. Although several processes regulated by HBGF are altered in Alzheimer's disease, it is unknown whether the brain GAG capacities to bind and regulate the function of HBGF or of other heparin binding proteins, as tau, are modified in this disease. Here, we show that total sulfated GAGs from hippocampus of Alzheimer's disease have altered capacities to bind and potentiate the activities of growth factors including FGF-2, VEGF, and BDNF while their capacity to bind to tau is remarkable increased. Alterations of GAG structures and capacities to interact with and regulate the activity of heparin binding proteins might contribute to impaired tissue homeostasis in the Alzheimer's disease brain.
糖胺聚糖(GAGs),包括肝素硫酸盐和软骨素硫酸盐,是细胞外基质的主要成分。与肝素结合生长因子(HBGF)相互作用时,GAGs 参与维持组织内稳态,并有助于自我修复。尽管阿尔茨海默病中几种受 HBGF 调节的过程发生改变,但尚不清楚大脑 GAG 结合和调节 HBGF 或其他肝素结合蛋白(如 tau)功能的能力是否在这种疾病中发生改变。在这里,我们发现来自阿尔茨海默病患者海马体的总硫酸化 GAG 结合和增强包括 FGF-2、VEGF 和 BDNF 在内的生长因子活性的能力发生了改变,而其与 tau 结合的能力显著增加。GAG 结构的改变以及与肝素结合蛋白相互作用和调节其活性的能力的改变,可能导致阿尔茨海默病大脑组织内稳态受损。