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1,25-二羟基维生素D3对人脂肪间充质干细胞的脂肪生成具有剂量依赖性调节作用。

1,25-Dihydroxyvitamin D3 modulates adipogenesis of human adipose-derived mesenchymal stem cells dose-dependently.

作者信息

Salehpour Amin, Hedayati Mehdi, Shidfar Farzad, Neshatbini Tehrani Asal, Farshad Ali Asghar, Mohammadi Saeed

机构信息

Occupational Health Research Center, School of Public Health, Iran University of Medical Sciences, Tehran, Iran.

Cellular and Molecular Endocrine Research Center, Research Institute for Endocrine Sciences, Shahid Beheshti University of Medical Sciences, 2nd Floor, Number 24, Parvaneh Street, Yemen Street, Chamran Exp, Tehran, Iran.

出版信息

Nutr Metab (Lond). 2021 Mar 12;18(1):29. doi: 10.1186/s12986-021-00561-4.

Abstract

PURPOSE

1,25-dihydroxyvitamin D3 may regulate adipogenesis in adipocytes in-vitro, but little is known about possible molecular mechanisms related to the inhibitory effect of 1,25-dihydroxyvitamin D3 on adipogenesis in humans҆ adipose tissue.

METHODOLOGY

In this study, human adipose-derived mesenchymal stem cells (hASCs) were cultured for 14 days in adipogenic differentiation media containing concentrations of 1,25-dihydroxyvitamin D3 (10-10 M). The extent of adipogenic differentiation in ASCs was assessed by Oil Red O staining and quantitative polymerase chain reaction (PCR) to determine expression levels of key adipogenic markers.

RESULTS

Our results showed that vitamin D receptor (VDR), as a mediator of most actions of 1,25-dihydroxyvitamin D3, glucose trasporter-4 (GLUT4),and fatty acid binding protein-4 (FABP4) was expressed in vitamin D-treated hASCs. However, the protein level of these markers was lower than the control group. Treatment of human preadipocytes with 1,25-dihydroxyvitamin D3 significantly altered expression of adipogenic markers and triglyceride accumulation in a dose-dependent manner. 1,25-dihydroxyvitamin D3 at concentration of 10 M enhanced expression of sterol regulatory element-binding protein-1c (SREBP1c), CCAAT-enhancer-binding protein-β (C/EBPβ), a mitotic clonal expansion, peroxisome proliferator-activated receptor-gamma (PPARγ), fatty acid synthase (FASN), a marker of de novo lipogenesis,and lipoprotein lipase (LPL).

CONCLUSION

Our findings revealed that 1,25-dihydroxyvitamin D3 may provoke adipocyte development in critical periods of adipogenesis at concentration of 10 M, thereby leading to a greater risk of obesity in adulthood and an augmented risk of obesity-related diseases including diabetes, cardiovascular diseases, and some cancers.

摘要

目的

1,25 - 二羟基维生素D3可能在体外调节脂肪细胞的脂肪生成,但对于1,25 - 二羟基维生素D3对人体脂肪组织脂肪生成抑制作用的相关分子机制知之甚少。

方法

在本研究中,将人脂肪来源的间充质干细胞(hASCs)在含有1,25 - 二羟基维生素D3(10 - 10 M)浓度的成脂分化培养基中培养14天。通过油红O染色和定量聚合酶链反应(PCR)评估脂肪干细胞中脂肪生成分化的程度,以确定关键脂肪生成标志物的表达水平。

结果

我们的结果表明,维生素D受体(VDR)作为1,25 - 二羟基维生素D3大多数作用的介质、葡萄糖转运蛋白4(GLUT4)和脂肪酸结合蛋白4(FABP4)在维生素D处理的hASCs中表达。然而,这些标志物的蛋白质水平低于对照组。用1,25 - 二羟基维生素D3处理人前脂肪细胞以剂量依赖方式显著改变脂肪生成标志物的表达和甘油三酯积累。浓度为10 M的1,25 - 二羟基维生素D3增强了固醇调节元件结合蛋白1c(SREBP1c)、CCAAT增强子结合蛋白β(C/EBPβ)、有丝分裂克隆扩增、过氧化物酶体增殖物激活受体γ(PPARγ)、脂肪酸合酶(FASN)(一种从头脂肪生成的标志物)和脂蛋白脂肪酶(LPL)的表达。

结论

我们的研究结果表明,1,25 - 二羟基维生素D3在浓度为10 M时可能在脂肪生成的关键时期促进脂肪细胞发育,从而导致成年期肥胖风险增加以及包括糖尿病、心血管疾病和某些癌症在内的肥胖相关疾病风险增加。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c3c8/7953614/50422532e3fa/12986_2021_561_Fig1_HTML.jpg

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