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Expression of familial Alzheimer disease presenilin 1 gene attenuates vesicle traffic and reduces peptide secretion in cultured astrocytes devoid of pathologic tissue environment

机译:家族性阿尔茨海默病早老素1基因的表达减弱囊泡运输并减少缺乏病理组织环境的培养星形胶质细胞中的肽分泌

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摘要

In the brain, astrocytes provide metabolic and trophic support to neurones. Failure in executing astroglial homeostatic functions may contribute to the initiation and propagation of diseases, including Alzheimer disease (AD), characterized by a progressive loss of neurones over years. Here, we examined whether astrocytes from a mice model of AD isolated in the presymptomatic phase of the disease exhibit alterations in vesicle traffic, vesicular peptide release and purinergic calcium signaling. In cultured astrocytes isolated from a newborn wild-type (wt) and 3xTg-AD mouse, secretory vesicles and acidic endosomes/lysosomes were labeled by transfection with plasmid encoding atrial natriuretic peptide tagged with mutant green fluorescent protein (ANP.emd) and by LysoTracker, respectively. The intracellular Ca2+ concentration ([Ca2+]i) was monitored with Fluo-2 and visualized by confocal microscopy. In comparison with controls, spontaneous mobility of ANP- and LysoTracker-labeled vesicles was diminished in 3xTg-AD astrocytes; the track length (TL), maximal displacement (MD) and directionality index (DI) were all reduced in peptidergic vesicles and in endosomes/lysosomes (P <0.001), as was the ATP-evoked attenuation of vesicle mobility. Similar impairment of peptidergic vesicle trafficking was observed in wt rat astrocytes transfected to express mutated presenilin 1 (PS1M146V). The ATP-evoked ANP discharge from single vesicles was less efficient in 3xTg-AD and PS1M146V-expressing astrocytes than in respective wt controls (P <0.05). Purinergic stimulation evoked biphasic and oscillatory [Ca2+]i responses; the latter were less frequent (P <0.001) in 3xTg-AD astrocytes. Expression of PS1M146V in astrocytes impairs vesicle dynamics and reduces evoked secretion of the signaling molecule ANP; both may contribute to the development of AD. GLIA 2015
机译:在大脑中,星形胶质细胞为神经元提供代谢和营养支持。执行星形胶质体内稳态功能失败可能会导致疾病的发生和传播,包括阿尔茨海默病(AD),其特征是多年来神经元逐渐丧失。在这里,我们检查了在疾病的症状前期分离的AD小鼠模型中的星形胶质细胞是否在囊泡运输,囊泡肽释放和嘌呤能钙信号传导方面表现出改变。在从新生野生型(wt)和3xTg-AD小鼠分离的培养的星形胶质细胞中,通过用编码带有突变绿色荧光蛋白(ANP.emd)的心房利钠肽的质粒转染并通过LysoTracker来标记分泌性囊泡和酸性内体/溶酶体, 分别。用Fluo-2监测细胞内Ca2 +浓度([Ca2 +] i),并通过共聚焦显微镜观察。与对照相比,在3xTg-AD星形胶质细胞中,ANP和LysoTracker标记的囊泡的自发迁移性降低了。肽能性囊泡和内体/溶酶体的轨道长度(TL),最大位移(MD)和方向性指数(DI)均降低(P <0.001),ATP引起的囊泡运动性减弱也降低。在wt大鼠星形胶质细胞转染表达突变的早老素1(PS1M146V)中观察到类似的肽能小泡运输受损。在表达3xTg-AD和PS1M146V的星形胶质细胞中,由ATP引起的单囊泡ANP排放效率低于相应的wt对照(P <0.05)。嘌呤能刺激引起双相和振荡性[Ca2 +] i反应。后者在3xTg-AD星形胶质细胞中的频率较低(P <0.001)。星形胶质细胞中PS1M146V的表达削弱囊泡动力学,并减少信号分子ANP的诱发分泌;两者都可能有助于AD的发展。 GLIA 2015

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