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机械应变通过刺激持久的β-连环蛋白信号来抑制间充质干细胞的脂肪生成。

Mechanical strain inhibits adipogenesis in mesenchymal stem cells by stimulating a durable beta-catenin signal.

作者信息

Sen Buer, Xie Zhihui, Case Natasha, Ma Meiyun, Rubin Clinton, Rubin Janet

机构信息

Department of Medicine, University of North Carolina, Chapel Hill, North Carolina 27599, USA.

出版信息

Endocrinology. 2008 Dec;149(12):6065-75. doi: 10.1210/en.2008-0687. Epub 2008 Aug 7.

Abstract

The ability of exercise to decrease fat mass and increase bone mass may occur through mechanical biasing of mesenchymal stem cells (MSCs) away from adipogenesis and toward osteoblastogenesis. C3H10T1/2 MSCs cultured in highly adipogenic medium express peroxisome proliferator-activated receptor gamma and adiponectin mRNA and protein, and accumulate intracellular lipid. Mechanical strain applied for 6 h daily inhibited expression of peroxisome proliferator-activated receptor gamma and adiponectin mRNA by up to 35 and 50%, respectively, after 5 d. A decrease in active and total beta-catenin levels during adipogenic differentiation was entirely prevented by daily application of mechanical strain; furthermore, strain induced beta-catenin nuclear translocation. Inhibition of glycogen synthase kinase-3beta by lithium chloride or SB415286 also prevented adipogenesis, suggesting that preservation of beta-catenin levels was important to strain inhibition of adipogenesis. Indeed, mechanical strain inactivated glycogen synthase kinase-3beta, which was preceded by Akt activation, indicating that strain transmits antiadipogenic signals through this pathway. Cells grown under adipogenic conditions showed no increase in osteogenic markers runt-related transcription factor (Runx) 2 and osterix (Osx); subsequent addition of bone morphogenetic protein 2 for 2 d increased Runx2 but not Osx expression in unstrained cultures. When cultures were strained for 5 d before bone morphogenetic protein 2 addition, Runx2 mRNA increased more than in unstrained cultures, and Osx expression more than doubled. As such, mechanical strain enhanced MSC potential to enter the osteoblast lineage despite exposure to adipogenic conditions. Our results indicate that MSC commitment to adipogenesis can be suppressed by mechanical signals, allowing other signals to promote osteoblastogenesis. These data suggest that positive effects of exercise on both fat and bone may occur during mesenchymal lineage selection.

摘要

运动减少脂肪量并增加骨量的能力可能是通过对间充质干细胞(MSC)进行机械性偏向,使其远离脂肪生成并趋向成骨细胞生成。在高度成脂培养基中培养的C3H10T1/2 MSC表达过氧化物酶体增殖物激活受体γ和脂联素的mRNA及蛋白质,并积累细胞内脂质。每天施加6小时的机械应变,5天后分别使过氧化物酶体增殖物激活受体γ和脂联素mRNA的表达抑制高达35%和50%。在成脂分化过程中,每天施加机械应变可完全阻止活性β-连环蛋白和总β-连环蛋白水平的降低;此外,应变诱导β-连环蛋白核转位。用氯化锂或SB415286抑制糖原合酶激酶-3β也可阻止脂肪生成,这表明维持β-连环蛋白水平对应变抑制脂肪生成很重要。事实上,机械应变使糖原合酶激酶-3β失活,这之前Akt被激活,表明应变通过该途径传递抗脂肪生成信号。在成脂条件下生长的细胞,其成骨标志物 runt相关转录因子(Runx)2和osterix(Osx)没有增加;随后在未受应变的培养物中添加骨形态发生蛋白2 2天,可增加Runx2的表达,但不增加Osx的表达。当在添加骨形态发生蛋白2之前对培养物施加5天应变时,Runx2 mRNA的增加比未受应变的培养物更多,且Osx的表达增加了一倍多。因此,尽管暴露于成脂条件下,机械应变仍增强了MSC进入成骨细胞谱系的潜能。我们的结果表明,机械信号可抑制MSC向脂肪生成的定向分化,使其他信号促进成骨细胞生成。这些数据表明,运动对脂肪和骨骼的积极影响可能发生在间充质谱系选择过程中。

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