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

Authors :
Choi KJ
Lee JH
Park SB
Na YJ
Jung WH
Lee H
Kim KY
Source :
Journal of pharmacological sciences [J Pharmacol Sci] 2022 Apr; Vol. 148 (4), pp. 377-386. Date of Electronic Publication: 2022 Feb 16.
Publication Year :
2022

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.<br />Competing Interests: Declaration of competing interest The authors indicated no potential conflicts of interest.<br /> (Copyright © 2022 The Authors. Production and hosting by Elsevier B.V. All rights reserved.)

Details

Language :
English
ISSN :
1347-8648
Volume :
148
Issue :
4
Database :
MEDLINE
Journal :
Journal of pharmacological sciences
Publication Type :
Academic Journal
Accession number :
35300813
Full Text :
https://doi.org/10.1016/j.jphs.2022.02.002