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利用三维干细胞衍生神经模型研究银杏叶提取物(EGb761)衍生的类黄酮单体的神经保护功能。

Study of neuroprotective function of Ginkgo biloba extract (EGb761) derived-flavonoid monomers using a three-dimensional stem cell-derived neural model.

作者信息

Wu Yueting, Sun Jiachen, George Julian, Ye Hua, Cui Zhanfeng, Li Zhaohui, Liu Qingxi, Zhang Yaozhou, Ge Dan, Liu Yang

机构信息

Tianjin University of Traditional Chinese Medicine, Tianjin, 300193, China.

Tianjin International Joint Academy of Biomedicine, Tianjin, 300457, China.

出版信息

Biotechnol Prog. 2016 May;32(3):735-44. doi: 10.1002/btpr.2255. Epub 2016 Mar 12.

Abstract

An in vitro three-dimensional (3D) cell culture system that can mimic organ and tissue structure and function in vivo will be of great benefit for drug discovery and toxicity testing. In this study, the neuroprotective properties of the three most prevalent flavonoid monomers extracted from EGb 761 (isorharmnetin, kaempferol, and quercetin) were investigated using the developed 3D stem cell-derived neural co-culture model. Rat neural stem cells were differentiated into co-culture of both neurons and astrocytes at an equal ratio in the developed 3D model and standard two-dimensional (2D) model using a two-step differentiation protocol for 14 days. The level of neuroprotective effect offered by each flavonoid was found to be aligned with its effect as an antioxidant and its ability to inhibit Caspase-3 activity in a dose-dependent manner. Cell exposure to quercetin (100 µM) following oxidative insult provided the highest levels of neuroprotection in both 2D and 3D models, comparable with exposure to 100 µM of Vitamin E, whilst exposure to isorhamnetin and kaempferol provided a reduced level of neuroprotection in both 2D and 3D models. At lower dosages (10 µM flavonoid concentration), the 3D model was more representative of results previously reported in vivo. The co-cultures of stem cell derived neurons and astrocytes in 3D hydrogel scaffolds as an in vitro neural model closely replicates in vivo results for routine neural drug toxicity and efficacy testing. © 2016 American Institute of Chemical Engineers Biotechnol. Prog., 32:735-744, 2016.

摘要

一种能够模拟体内器官和组织结构及功能的体外三维(3D)细胞培养系统,将对药物研发和毒性测试大有裨益。在本研究中,使用已开发的3D干细胞衍生神经共培养模型,研究了从银杏叶提取物761(异鼠李素、山柰酚和槲皮素)中提取的三种最常见黄酮类单体的神经保护特性。使用两步分化方案,将大鼠神经干细胞在已开发的3D模型和标准二维(2D)模型中以相等比例分化为神经元和星形胶质细胞的共培养物,持续14天。发现每种黄酮类化合物提供的神经保护作用水平与其作为抗氧化剂的作用及其以剂量依赖性方式抑制半胱天冬酶-3活性的能力相一致。在氧化损伤后,细胞暴露于槲皮素(100µM)在2D和3D模型中均提供了最高水平的神经保护,与暴露于100µM维生素E相当,而暴露于异鼠李素和山柰酚在2D和3D模型中提供的神经保护水平较低。在较低剂量(黄酮类化合物浓度为10µM)下,3D模型更能代表先前在体内报道的结果。作为体外神经模型的3D水凝胶支架中干细胞衍生的神经元和星形胶质细胞的共培养物,紧密复制了体内常规神经药物毒性和疗效测试的结果。©2016美国化学工程师学会生物技术进展,32:735-744,2016。

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