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活跃的γ-分泌酶在大鼠脑组织中的突触和内体定位。

Synaptic and endosomal localization of active gamma-secretase in rat brain.

机构信息

Department of Neurobiology, Care Sciences and Society (NVS), Karolinska Institutet Dainippon Sumitomo Pharma Alzheimer Center, Novum, Huddinge, Sweden.

出版信息

PLoS One. 2010 Jan 28;5(1):e8948. doi: 10.1371/journal.pone.0008948.

Abstract

BACKGROUND

A key player in the development of Alzheimer's disease (AD) is the gamma-secretase complex consisting of at least four components: presenilin, nicastrin, Aph-1 and Pen-2. gamma-Secretase is crucial for the generation of the neurotoxic amyloid beta-peptide (Abeta) but also takes part in the processing of many other substrates. In cell lines, active gamma-secretase has been found to localize primarily to the Golgi apparatus, endosomes and plasma membranes. However, no thorough studies have been performed to show the subcellular localization of the active gamma-secretase in the affected organ of AD, namely the brain.

PRINCIPAL FINDINGS

We show by subcellular fractionation of rat brain that high gamma-secretase activity, as assessed by production of Abeta40, is present in an endosome- and plasma membrane-enriched fraction of an iodixanol gradient. We also prepared crude synaptic vesicles as well as synaptic membranes and both fractions showed high Abeta40 production and contained high amounts of the gamma-secretase components. Further purification of the synaptic vesicles verified the presence of the gamma-secretase components in these compartments. The localization of an active gamma-secretase in synapses and endosomes was confirmed in rat brain sections and neuronal cultures by using a biotinylated gamma-secretase inhibitor together with confocal microscopy.

SIGNIFICANCE

The information about the subcellular localization of gamma-secretase in brain is important for the understanding of the molecular mechanisms of AD. Furthermore, the identified fractions can be used as sources for highly active gamma-secretase.

摘要

背景

阿尔茨海默病(AD)发展的关键因素是γ-分泌酶复合物,它由至少四个成分组成:早老素、尼卡斯特林、APH-1 和 PEN-2。γ-分泌酶对于神经毒性淀粉样β肽(Abeta)的产生至关重要,但也参与了许多其他底物的加工。在细胞系中,活性 γ-分泌酶主要定位于高尔基体、内体和质膜。然而,尚无彻底的研究表明活性 γ-分泌酶在 AD 受累器官(即大脑)中的亚细胞定位。

主要发现

我们通过大鼠脑的亚细胞分级分离表明,高 γ-分泌酶活性(如 Abeta40 的产生所评估)存在于碘克沙醇梯度中的内体和质膜丰富级分中。我们还制备了粗突触小泡以及突触膜,这两种级分均显示出高 Abeta40 的产生,并含有大量的 γ-分泌酶成分。突触小泡的进一步纯化证实了这些隔室中存在 γ-分泌酶成分。通过使用生物素化的 γ-分泌酶抑制剂和共聚焦显微镜,在大鼠脑切片和神经元培养物中证实了活性 γ-分泌酶在突触和内体中的定位。

意义

关于 γ-分泌酶在大脑中的亚细胞定位的信息对于理解 AD 的分子机制非常重要。此外,鉴定的级分可用作高度活跃的 γ-分泌酶的来源。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d30e/2812513/5af6d7bfce46/pone.0008948.g001.jpg

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