Proteomic analysis reveals that the protective effects of ginsenoside Rb1 are associated with the actin cytoskeleton in β-amyloid-treated neuronal cells

被引:22
作者
Hwang, Ji Yeon [1 ]
Shim, Ji Seon [1 ]
Song, Min-Young [1 ]
Yim, Sung-Vin [2 ]
Lee, Seung Eun [3 ]
Park, Kang-Sik [1 ]
机构
[1] Kyung Hee Univ, Sch Med, Dept Physiol, 26 Kyungheedae Ro, Seoul 02447, South Korea
[2] Kyung Hee Univ, Sch Med, Dept Clin Pharmacol, Seoul, South Korea
[3] Natl Inst Hort & Herbal Sci, Dept Herbal Crop Res, Eumseong, South Korea
关键词
actin skeleton; Alzheimer's disease; beta-amyloid; ginsenoside Rb1; mass spectrometry; ALZHEIMERS-DISEASE; ANIMAL-MODELS; COFILIN; CAP1; NEURODEGENERATION; EXPRESSION; DATABASE; DESTRIN; RB-1; RG1;
D O I
10.1016/j.jgr.2015.09.004
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Background: The ginsenoside Rb1 (Rb1) is the most abundant compound in the root of Panax ginseng. Recent studies have shown that Rb1 has a neuroprotective effect. However, the mechanisms underlying this effect are still unknown. Methods: We used stable isotope labeling with amino acids in cell culture, combined with quantitative mass spectrometry, to explore a potential protective mechanism of Rb1 in beta-amyloid-treated neuronal cells. Results: A total of 1,231 proteins were commonly identified from three replicate experiments. Among these, 40 proteins were significantly changed in response to Rb1 pretreatment in beta-amyloid-treated neuronal cells. Analysis of the functional enrichments and protein interactions of altered proteins revealed that actin cytoskeleton proteins might be linked to the regulatory mechanisms of Rb1. The CAP1, CAPZB, TOMM40, and DSTN proteins showed potential as molecular target proteins for the functional contribution of Rb1 in Alzheimer's disease (AD). Conclusion: Our proteomic data may provide new insights into the protective mechanisms of Rb1 in AD. Copyright (C) 2015, The Korean Society of Ginseng, Published by Elsevier.
引用
收藏
页码:278 / 284
页数:7
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