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人淀粉样β蛋白前体在转基因小鼠皮质中的突触营养作用。

Synaptotrophic effects of human amyloid beta protein precursors in the cortex of transgenic mice.

作者信息

Mucke L, Masliah E, Johnson W B, Ruppe M D, Alford M, Rockenstein E M, Forss-Petter S, Pietropaolo M, Mallory M, Abraham C R

机构信息

Department of Neuropharmacology, Scripps Research Institute, La Jolla, CA 92037.

出版信息

Brain Res. 1994 Dec 15;666(2):151-67. doi: 10.1016/0006-8993(94)90767-6.

Abstract

The amyloid precursor protein (APP) is involved in Alzheimer's disease (AD) because its degradation products accumulate abnormally in AD brains and APP mutations are associated with early onset AD. However, its role in health and disease appears to be complex, with different APP derivatives showing either neurotoxic or neurotrophic effects in vitro. To elucidate the effects APP has on the brain in vivo, cDNAs encoding different forms of human APP (hAPP) were placed downstream of the neuron-specific enolase (NSE) promoter. In multiple lines of NSE-hAPP transgenic mice neuronal overexpression of hAPP was accompanied by an increase in the number of synaptophysin immunoreactive (SYN-IR) presynaptic terminals and in the expression of the growth-associated marker GAP-43. In lines expressing moderate levels of hAPP751 or hAPP695, this effect was more prominent in homozygous than in heterozygous transgenic mice. In contrast, a line with several-fold higher levels of hAPP695 expression showed less increase in SYN-IR presynaptic terminals per amount of hAPP expressed than the lower expressor lines and a decrease in synaptotrophic effects in homozygous compared with heterozygous offspring. Transgenic mice (2-24 months of age) showed no evidence for amyloid deposits or neurodegeneration. These findings suggest that APP may be important for the formation/maintenance of synapses in vivo and that its synaptotrophic effects may be critically dependent on the expression levels of different APP isoforms. Alterations in APP expression, processing or function could contribute to the synaptic pathology seen in AD.

摘要

淀粉样前体蛋白(APP)与阿尔茨海默病(AD)相关,因为其降解产物在AD患者大脑中异常积累,且APP突变与早发性AD有关。然而,它在健康和疾病中的作用似乎很复杂,不同的APP衍生物在体外表现出神经毒性或神经营养作用。为了阐明APP在体内对大脑的影响,将编码不同形式人类APP(hAPP)的cDNA置于神经元特异性烯醇化酶(NSE)启动子的下游。在多株NSE-hAPP转基因小鼠中,hAPP的神经元过表达伴随着突触素免疫反应性(SYN-IR)突触前终末数量的增加以及生长相关标志物GAP-43表达的增加。在表达中等水平hAPP751或hAPP695的品系中,这种效应在纯合子转基因小鼠中比在杂合子转基因小鼠中更明显。相比之下,一个hAPP695表达水平高出几倍的品系,每表达量的hAPP中SYN-IR突触前终末的增加量比低表达品系少,并且与杂合子后代相比,纯合子的突触营养作用降低。转基因小鼠(2至24个月大)没有淀粉样沉积物或神经退行性变的证据。这些发现表明,APP可能对体内突触的形成/维持很重要,并且其突触营养作用可能严重依赖于不同APP异构体的表达水平。APP表达、加工或功能的改变可能导致AD中所见的突触病理学。

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