Cord lining progenitor cells: potential in vitro adipogenesis model

被引:4
作者
Cheong, H. H. [2 ]
Masilamani, J. [1 ]
Phan, T. T. [1 ,3 ]
Chan, S. Y. [2 ]
机构
[1] Natl Univ Singapore, Yong Loo Lin Sch Med, Dept Surg, Singapore 119074, Singapore
[2] Natl Univ Singapore, Dept Pharm, Singapore 117543, Singapore
[3] CellRes Corp Pte Ltd, Singapore, Singapore
关键词
cord lining; mesenchymal; adipocyte; differentiation; MESENCHYMAL STEM-CELLS; LEPTIN CONCENTRATIONS; ADIPOSE-TISSUE; NORMAL-WEIGHT; DIFFERENTIATION; ADIPSIN; EXPRESSION; ADIPONECTIN; PROTEIN; OBESITY;
D O I
10.1038/ijo.2010.86
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: To investigate the effect of glucose and insulin concentrations on differentiation of umbilical cord lining progenitor cells to adipocyte-like cells (ALCs). Methods: Cord lining mesenchymal cells (CLMCs) were isolated from the explant of human umbilical cord amniotic membrane. CLMCs were subjected to differentiation under various culture conditions for 20 days. Lipid droplets were confirmed with Oil Red O staining. Gene expressions of adipsin and peroxisome proliferator-activated receptor gamma (PPAR gamma) were analyzed using reverse transcription-PCR. Leptin and adiponectin secretions were detected using enzyme-linked immunosorbent assay kit. Results: CLMCs became irregular, cuboidal-shaped cells that resemble adipocytes, and Oil Red O staining showed the presence of lipid droplets. The gene expressions of PPAR gamma and adipsin were upregulated. Leptin and adiponectin secretions by naive CLMCs were below the limits of detection. Matured ALCs cultured in low-glucose medium significantly secreted leptin and adiponectin, whereas those in high-glucose medium significantly secreted only leptin. Insulin concentration affects leptin but not adiponectin secretion. Conclusions: Under different culture conditions, CLMCs can differentiate into ALCs that resemble adipocytes in either normal-weight or obese individuals. Hence, these ALCs have the potential to be used as an in vitro model to study adipogenesis and obesity, and possibly as a drug discovery model for metabolic disorders. International Journal of Obesity (2010) 34, 1625-1633; doi:10.1038/ijo.2010.86; published online 18 May 2010
引用
收藏
页码:1625 / 1633
页数:9
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