4.5 Article

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

期刊

JOURNAL OF PHARMACOLOGICAL SCIENCES
卷 148, 期 4, 页码 377-386

出版社

JAPANESE PHARMACOLOGICAL SOC
DOI: 10.1016/j.jphs.2022.02.002

关键词

Metabolic syndrome; Obesity; Insulin resistance; 3D culture; Drug screening

资金

  1. R&D Convergence Program of the National Research Council of Science Technology [CAP-15-10-KRICT]
  2. Technology Innovation Program the Ministry of Trade, Industry Energy [20009774]
  3. Korea Research Institute of Chemical Technology of Republic of Korea [SI2131-50, KK2132-10]

向作者/读者索取更多资源

Macrophages in adipose tissue contribute to metabolic disorders, and a 3D culture system was developed to study drug screening for anti-obesity effects.
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 PPAR gamma antagonist GW9662 (10, 20 mu M) repressed adipogenic differentiation in a concentration-dependent manner in 3D co-cultured cells. (C) 2022 The Authors. Production and hosting by Elsevier B.V. on behalf of Japanese Pharmacological Society.

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