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人绒毛膜来源间充质干细胞在成脂分化过程中的基因表达模式。

Gene expression pattern of human chorion-derived mesenchymal stem cells during adipogenic differentiation.

机构信息

Department of Obstetrics and Gynecology, Uijeongbu St. Mary’s Hospital, School of Medicine, The Catholic University of Korea, Uijeongbu, Korea.

出版信息

Yonsei Med J. 2012 Sep;53(5):1036-44. doi: 10.3349/ymj.2012.53.5.1036.

Abstract

PURPOSE

The aim of this study was to identify the adipocyte-specific gene expression patterns in chorion-derived mesenchymal stem cells during adipogenic differentiation.

MATERIALS AND METHODS

Chorionic cells were isolated from the third trimester chorions from human placenta at birth and identified morphologically and by fluorescence-activated cell sorting analysis. After inducing adipogenic differentiation for 28 days, cells at days 3, 10, 21 and 28 were analyzed by Oil red O staining and RNA extraction in order to assess the expression levels of adipocyte marker genes, including CCAAT-enhancer binding protein α (C/EBPα), peroxisome proliferator- activated receptor γ (PPARγ), fatty acid binding protein 4 (FABP4) and Glycerol-3-phosphate dehydrogenase (GPD2). Cells not induced for differentiation were compared with the induced cells as a control group.

RESULTS

Chorion-derived cells showed the same pattern as fibroblasts, and expressed CD73, CD105, and CD166 antigens, but not CD45, CD34, and HLA-DR antigens. On day 3 after differentiation, cells began to stain positively upon Oil red O staining, and continuously increased in lipid granules for 4 weeks. The expression level of C/EBPα increased 4.6 fold on day 3 after induction, and continued to increase for 4 weeks. PPARγ was expressed at a maximum of 2.9 fold on day 21. FABP4 and GPD2 were significantly expressed at 4.7- and 3.0-fold, respectively, on day 21, compared to controls, and further increased thereafter.

CONCLUSION

Human chorion-derived mesenchymal stem cells exhibited the sequential expression pattern of adipocyte marker genes during differentiation, corresponding to adipogenesis.

摘要

目的

本研究旨在鉴定人胎盘绒毛膜来源间充质干细胞在脂肪生成分化过程中的脂肪细胞特异性基因表达模式。

材料与方法

从分娩时的人胎盘第三 trimester 绒毛膜中分离绒毛细胞,通过形态学和荧光激活细胞分选分析进行鉴定。在诱导脂肪生成分化 28 天后,在第 3、10、21 和 28 天通过油红 O 染色和 RNA 提取分析细胞,以评估脂肪细胞标记基因的表达水平,包括 CCAAT 增强子结合蛋白α(C/EBPα)、过氧化物酶体增殖物激活受体γ(PPARγ)、脂肪酸结合蛋白 4(FABP4)和甘油-3-磷酸脱氢酶(GPD2)。未诱导分化的细胞与诱导分化的细胞作为对照组进行比较。

结果

绒毛细胞表现出与成纤维细胞相同的模式,表达 CD73、CD105 和 CD166 抗原,但不表达 CD45、CD34 和 HLA-DR 抗原。分化后第 3 天,细胞开始油红 O 染色阳性,4 周内脂质颗粒不断增加。诱导后第 3 天 C/EBPα 的表达水平增加了 4.6 倍,并持续增加 4 周。PPARγ 在第 21 天表达最高,为 2.9 倍。FABP4 和 GPD2 在第 21 天分别显著表达 4.7 倍和 3.0 倍,与对照组相比,此后进一步增加。

结论

人绒毛膜来源间充质干细胞在分化过程中表现出脂肪细胞标记基因的顺序表达模式,与脂肪生成相对应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/14f9/3423845/e317192e162d/ymj-53-1036-g001.jpg

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