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虾青素可提高神经干细胞的增殖能力以及成骨和脂肪分化潜能。

Astaxanthin improves the proliferative capacity as well as the osteogenic and adipogenic differentiation potential in neural stem cells.

机构信息

Department of Biomaterial Control, Dong-Eui University, Busan, South Korea.

出版信息

Food Chem Toxicol. 2010 Jun;48(6):1741-5. doi: 10.1016/j.fct.2010.04.002. Epub 2010 Apr 9.

Abstract

In the present study, the effect of astaxanthin on improvement of the proliferative capacity as well as the osteogenic and adipogenic differentiation potential in neural stem cells (NSCs) was evaluated. Treatment of astaxanthin-induced actives cell growth in a dose-dependent and time-dependent manner. Results from a clonogenic assay clearly indicated that astaxanthin can actively stimulate proliferation of NSCs. Astaxanthin-induced improvement in the proliferative capacity of NSCs resulted in overexpression of several proliferation-related proteins. Astaxanthin-induced activation of PI3K and its downstream mediators, p-MEK, p-ERK, and p-Stat3 in NSCs resulted in subsequent induction of expression of proliferation-related transcription factors (Rex1, CDK1, and CDK2) and stemness genes (OCT4, SOX2, Nanog, and KLF4). Astaxanthin also improved the osteogenic and adipogenic differentiation potential of NSCs. Astaxanthin-treated NSCs showed prominent calcium deposits and fat formation. These results were consistent with overexpression of osteogenesis-related genes (osteonectin, RXR, and osteopontin) and adipogenesis-related genes (AP and PPAR-gamma) after astaxanthin treatment. These findings clearly demonstrated that astaxanthin acts synergistically on the regulatory circuitry that controls proliferation and differentiation of NSCs.

摘要

在本研究中,评估了虾青素对神经干细胞(NSCs)增殖能力以及成骨和脂肪分化潜能改善的影响。虾青素以剂量和时间依赖的方式治疗,诱导活性细胞生长。集落形成试验的结果清楚地表明,虾青素可以积极刺激 NSCs 的增殖。虾青素诱导的 NSCs 增殖能力的提高导致了几个与增殖相关的蛋白的过表达。虾青素诱导的 NSCs 中 PI3K 及其下游介质 p-MEK、p-ERK 和 p-Stat3 的激活导致了与增殖相关的转录因子(Rex1、CDK1 和 CDK2)和干性基因(OCT4、SOX2、Nanog 和 KLF4)的表达诱导。虾青素还改善了 NSCs 的成骨和脂肪分化潜能。虾青素处理的 NSCs 显示出明显的钙沉积和脂肪形成。这些结果与虾青素处理后成骨相关基因(骨桥蛋白、RXR 和骨粘连蛋白)和脂肪生成相关基因(AP 和 PPAR-γ)的过表达一致。这些发现清楚地表明,虾青素对控制 NSCs 增殖和分化的调节回路具有协同作用。

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