Dow K E, Riopelle R J
Department of Pediatrics, Queen's University, Kingston General Hospital, Ont., Canada.
Brain Res Dev Brain Res. 1994 Jul 15;80(1-2):175-82. doi: 10.1016/0165-3806(94)90102-3.
A human cell line committed to neuronal lineage was used to examine the influence of differentiation on proteoglycan synthesis and function. Where the LA-N-2 cells were stimulated to differentiate towards a phenotype of cholinergic neurons, proteoglycans of the heparan sulphate class increased relative to chondroitin sulphate proteoglycans and displayed more homogeneously shorter glycosaminoglycan chains with increasing degrees of sulphation. The changes were accompanied by increasing potency of the heparan sulphate proteoglycans in neurite growth-promoting activity when immobilized on a laminin substrate. These studies begin to address the role of activity-independent growth and differentiation on the synthesis and release by neurons of neurite growth-promoting proteoglycans. The observations have implications for understanding the role of proteoglycan overexpression and the production of dystrophic neurites in Alzheimer disease.
一种已确定向神经谱系分化的人类细胞系被用于研究分化对蛋白聚糖合成及功能的影响。当LA-N-2细胞被刺激向胆碱能神经元表型分化时,硫酸乙酰肝素类蛋白聚糖相对于硫酸软骨素蛋白聚糖增加,并且随着硫酸化程度的增加,显示出更均匀的较短糖胺聚糖链。这些变化伴随着固定在层粘连蛋白底物上时硫酸乙酰肝素蛋白聚糖促进神经突生长活性的增强。这些研究开始探讨与活性无关的生长和分化对神经突生长促进蛋白聚糖的合成和释放的作用。这些观察结果对于理解蛋白聚糖过表达的作用以及阿尔茨海默病中营养不良性神经突的产生具有重要意义。