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二氧化硅纳米颗粒通过调节p38磷酸化抑制棕色脂肪细胞分化。

Silica nanoparticles inhibit brown adipocyte differentiation via regulation of p38 phosphorylation.

作者信息

Son Min Jeong, Kim Won Kon, Kwak Minjeong, Oh Kyoung-Jin, Chang Won Seok, Min Jeong-Ki, Lee Sang Chul, Song Nam Woong, Bae Kwang-Hee

机构信息

Functional Genomics Research Center, KRIBB, Daejeon 305-806, Korea.

出版信息

Nanotechnology. 2015 Oct 30;26(43):435101. doi: 10.1088/0957-4484/26/43/435101. Epub 2015 Oct 5.

Abstract

Nanoparticles are of great interest due to their wide variety of biomedical and bioengineering applications. However, they affect cellular differentiation and/or intracellular signaling when applied and exposed to target organisms or cells. The brown adipocyte is a cell type important in energy homeostasis and thus closely related to obesity. In this study, we assessed the effects of silica nanoparticles (SNPs) on brown adipocyte differentiation. The results clearly showed that brown adipocyte differentiation was significantly repressed by exposure to SNPs. The brown adipocyte-specific genes as well as mitochondrial content were also markedly reduced. Additionally, SNPs led to suppressed p38 phosphorylation during brown adipocyte differentiation. These effects depend on the size of SNPs. Taken together, these results lead us to suggest that SNP has anti-brown adipogenic effect in a size-dependent manner via regulation of p38 phosphorylation.

摘要

纳米颗粒因其在生物医学和生物工程领域的广泛应用而备受关注。然而,当应用并暴露于靶生物体或细胞时,它们会影响细胞分化和/或细胞内信号传导。棕色脂肪细胞是一种在能量稳态中起重要作用的细胞类型,因此与肥胖密切相关。在本研究中,我们评估了二氧化硅纳米颗粒(SNPs)对棕色脂肪细胞分化的影响。结果清楚地表明,暴露于SNPs会显著抑制棕色脂肪细胞的分化。棕色脂肪细胞特异性基因以及线粒体含量也明显减少。此外,SNPs导致棕色脂肪细胞分化过程中p38磷酸化受到抑制。这些效应取决于SNPs的大小。综上所述,这些结果使我们认为,SNPs通过调节p38磷酸化,以大小依赖的方式具有抗棕色脂肪生成作用。

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