In vitro characterization of the effects of chronic insulin stimulation in mouse 3T3-L1 and human SGBS adipocytes

被引:8
|
作者
Rossi, A. [1 ]
Eid, M. [1 ]
Dodgson, J. [2 ]
Davies, G. [1 ]
Musial, B. [3 ]
Wabitsch, M. [4 ]
Church, C. [1 ]
Hornigold, D. C. [1 ]
机构
[1] AstraZeneca, Biosci Metab Res & Early Dev, Cardiovasc Renal & Metab CVRM, BioPharmaceut R&D, Granta Pk, Cambridge, England
[2] AstraZeneca, Biol Therapeut Antibody & Prot Engn, R&D, Cambridge, England
[3] AstraZeneca, Biosci Renal Res & Early Dev, Cardiovasc Renal & Metab CVRM, BioPharmaceut R&D, Cambridge, England
[4] Univ Med Ctr, Div Paediat Endocrinol & Diabet, Dept Paediat & Adolescent Med, Ulm, Germany
关键词
hyperinsulinemia; SGBS; glucose uptake; lipolysis; GLUCOSE-TRANSPORT; RESISTANCE; HYPERINSULINEMIA; CELLS; TRANSCRIPTION; HISTORY;
D O I
10.1080/21623945.2020.1798613
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Hyperinsulinemia is the hallmark of the development of insulin resistance and precedes the diagnosis of type 2 diabetes. Here we evaluated the effects of prolonged exposure (>= 4 days) to high insulin doses (150 nM)in vitroin two adipose cell types, mouse 3T3-L1 and human SGBS. Chronic insulin treatment significantly decreased lipid droplet size, insulin signalling and insulin-stimulated glucose uptake. 3T3-L1 displayed an increased basal glucose internalization following chronic insulin treatment, which was associated with increased GLUT1 expression. In addition, both cells showed increased basal lipolysis. In conclusion, we report the effects of prolonged hyperinsulinemia in 3T3-L1 and SGBS, highlighting similarities and discrepancies between the cell types, to be considered when using these cells to model insulin-induced insulin resistance.
引用
收藏
页码:415 / 426
页数:12
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