Department of Medical Pharmacology, Institute of Health Biosciences, The University of Tokushima Graduate School, 3-18-15 Kuramoto-cho, Tokushima City 770-8504, Japan.
J Biosci Bioeng. 2010 Mar;109(3):297-303. doi: 10.1016/j.jbiosc.2009.09.003. Epub 2009 Sep 24.
Various mechanical stimuli affect differentiation of mesoderm-derived cells such as osteoblasts or myoblasts, suggesting that adipogenesis may also be influenced by mechanical stimulation. However, effects of mechanical stimuli on adipogenesis are scarcely known. Compressive force was applied to a human preadipocyte cell line, SGBS. Levels of gene expression were estimated by real-time reverse transcription-polymerase chain reaction. The accumulation of lipids was evaluated by Sudan III or Oil Red O staining. In SGBS cells subjected to a compressive force of 226 Pa for 12 h before adipogenic induction, adipogenesis was inhibited. Compressive force immediately after adipogenic induction did not affect the adipogenesis. The expression of peroxisome proliferator-activated receptor (PPAR) gamma2 and CCAAT/enhancer binding protein (C/EBP) alpha mRNA during adipogenesis was inhibited by compressive force, whereas C/EBPbeta and C/EBPdelta mRNA levels were unaffected. In preadipocytes, compressive force increased mRNA levels of Krüppel-like factor 2, preadipocyte factor 1, WNT10b, and cyclooxygenase-2 (COX-2) which are known as negative regulators for the PPARgamma2 and C/EBPalpha genes. Furthermore, a COX-2 inhibitor completely reversed the inhibition of adipogenesis by compressive force. In conclusion, compressive force inhibited adipogenesis by suppressing expression of PPARgamma2 and C/EBPalpha in a COX-2-dependent manner.
各种机械刺激会影响间充质来源的细胞(如成骨细胞或成肌细胞)的分化,这表明脂肪生成也可能受到机械刺激的影响。然而,机械刺激对脂肪生成的影响鲜为人知。本研究对人前体脂肪细胞系 SGBS 施加压缩力。通过实时逆转录聚合酶链反应估计基因表达水平。通过苏丹 III 或油红 O 染色评估脂质的积累。在诱导脂肪生成前,将 SGBS 细胞施加 226Pa 的压缩力 12 小时,脂肪生成受到抑制。脂肪生成诱导后立即施加的压缩力不会影响脂肪生成。在脂肪生成过程中,过氧化物酶体增殖物激活受体(PPAR)γ2 和 CCAAT/增强子结合蛋白(C/EBP)α mRNA 的表达受到压缩力的抑制,而 C/EBPβ 和 C/EBPδ mRNA 水平不受影响。在前体脂肪细胞中,压缩力增加了 Krüppel 样因子 2、前体脂肪因子 1、WNT10b 和环氧化酶-2(COX-2)的 mRNA 水平,这些因子已知是 PPARγ2 和 C/EBPα 基因的负调控因子。此外,COX-2 抑制剂完全逆转了压缩力对脂肪生成的抑制作用。综上所述,压缩力通过 COX-2 依赖性方式抑制 PPARγ2 和 C/EBPα 的表达来抑制脂肪生成。