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肥胖相关代谢综合征的体外三维药物筛选系统的开发。

Development of in vitro three-dimensional drug screening system for obesity-related metabolic syndrome.

机构信息

Therapeutics & Biotechnology Division, Korea Research Institute of Chemical Technology, P.O. Box 107, Yuseong-gu, Daejeon 34114, Republic of Korea.

Therapeutics & Biotechnology Division, Korea Research Institute of Chemical Technology, P.O. Box 107, Yuseong-gu, Daejeon 34114, Republic of Korea; Graduate School of New Drug Discovery and Development, Chungnam National University, 99 Daehak-ro, Yuseong-gu, Daejeon 34134, Republic of Korea.

出版信息

J Pharmacol Sci. 2022 Apr;148(4):377-386. doi: 10.1016/j.jphs.2022.02.002. Epub 2022 Feb 16.

Abstract

Metabolic syndrome is increasingly common, and closely related with overweight or obesity. In the obese state, macrophages infiltrate to the adipose tissue (AT), resulting in chronic inflammation and insulin resistance in the AT cells. Recently, attention has been paid to the role of AT macrophages in metabolic disorders should be applied to the initial drug screening step, but it was difficult to mimic the inflammatory adipocytes using the traditional 2-dimensional (2D) culture. In this study, we developed the 3-dimensional (3D) culture system to overcome this limitation. After adipogenic differentiation, lipid droplets were highly accumulated in cells, and differentiation of preadipocytes was not declined by macrophage co-culture. However, only co-cultured cells expressed the insulin resistance features. Compare to mono-cultured adipocytes, co-cultured adipocytes showed reduced glucose uptake and GLUT4 did not translocated to cell membrane even though treatment of high concentration of insulin. Using 3D co-culture model, we develop a microwell-scale drug screening protocol to test anti-obesity effect. 3D cultured cells reacted more sensitive to drugs, and PPARγ antagonist GW9662 (10, 20 μM) repressed adipogenic differentiation in a concentration-dependent manner in 3D co-cultured cells.

摘要

代谢综合征越来越常见,与超重或肥胖密切相关。在肥胖状态下,巨噬细胞浸润到脂肪组织(AT),导致 AT 细胞的慢性炎症和胰岛素抵抗。最近,人们开始关注 AT 巨噬细胞在代谢紊乱中的作用,应该将其应用于初始药物筛选步骤,但使用传统的二维(2D)培养方法很难模拟炎症性脂肪细胞。在这项研究中,我们开发了 3 维(3D)培养系统来克服这一限制。在脂肪生成分化后,细胞内大量积累脂质滴,巨噬细胞共培养不会降低前脂肪细胞的分化。然而,只有共培养的细胞表现出胰岛素抵抗的特征。与单核培养的脂肪细胞相比,共培养的脂肪细胞即使在高浓度胰岛素处理下,葡萄糖摄取减少,GLUT4 也不会转位到细胞膜。使用 3D 共培养模型,我们开发了一种微孔尺度的药物筛选方案来测试抗肥胖效果。3D 培养的细胞对药物的反应更敏感,PPARγ 拮抗剂 GW9662(10、20μM)在 3D 共培养细胞中以浓度依赖的方式抑制脂肪生成分化。

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