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缺乏淀粉样前体蛋白(APP)和类APP蛋白2的小鼠中突触小泡密度和活性区大小降低。

Reduced synaptic vesicle density and active zone size in mice lacking amyloid precursor protein (APP) and APP-like protein 2.

作者信息

Yang Guang, Gong Yan-Dao, Gong Kai, Jiang Wu-Ling, Kwon Elaine, Wang Pei, Zheng Hui, Zhang Xiu-Fang, Gan Wen-Biao, Zhao Nan-Ming

机构信息

State Key Lab of Biomembrane and Membrane Biotechnology, Department of Biological Sciences and Biotechnology, Tsinghua University, Beijing, China.

出版信息

Neurosci Lett. 2005;384(1-2):66-71. doi: 10.1016/j.neulet.2005.04.040.

Abstract

Although abnormal processing of amyloid precursor protein (APP) leads to early onset of Alzheimer's disease, the normal function of this protein is poorly understood. APP is widely expressed in axons, dendrites, and synapses in both central and peripheral nervous systems. Mice homozygous for APP or its homologue APP-like protein 2 (APLP2) null mutation (KO) are viable, but double mutants for APP and APLP2 deletions (DKO) are early postnatal lethal. To investigate the role of APP in synapse development, we compared the ultrastructure of submandibular ganglion synapses between DKO and littermate APLP2 KO mice at birth. Using serial electron microscopy, we found that the size of presynaptic boutons and the number of active zones per bouton were comparable in both strains of animals. However, the synaptic vesicle density, active zone size, and docked vesicle number per active zone were significantly reduced in DKO compared to those in APLP2 KO. These results indicate that the APP family of proteins plays an important role in regulating the formation and function of inter-neuronal synapses.

摘要

尽管淀粉样前体蛋白(APP)的异常加工会导致早发性阿尔茨海默病,但该蛋白的正常功能却鲜为人知。APP在中枢和外周神经系统的轴突、树突和突触中广泛表达。APP或其同源物类APP蛋白2(APLP2)纯合缺失突变(KO)的小鼠能够存活,但APP和APLP2双缺失突变体(DKO)在出生后早期致死。为了研究APP在突触发育中的作用,我们比较了出生时DKO小鼠和同窝APLP2 KO小鼠下颌下神经节突触的超微结构。通过连续电子显微镜观察,我们发现两种品系动物的突触前终扣大小和每个终扣的活性区数量相当。然而,与APLP2 KO相比,DKO中的突触小泡密度、活性区大小和每个活性区对接的小泡数量显著降低。这些结果表明,APP蛋白家族在调节神经元间突触的形成和功能中起重要作用。

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