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KATP channels in mesenchymal stromal stem cells: strong up-regulation of Kir6.2 subunits upon osteogenic differentiation.

机译:间充质基质干细胞中的KATP通道:成骨分化后Kir6.2亚基的强烈上调。

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The promising use of mesenchymal stromal cells (MSC) in regenerative technologies accounts for necessity of detailed study of their physiology. Proliferation and differentiation of multipotent cells often involve changes in their metabolic state. In the present study, we analyzed the expression of ATP-sensitive potassium (K(ATP)) channels in MSC and upon in vitro differentiation. K(ATP) channels are present in many cells and regulate a variety of cellular functions by coupling cell metabolism with membrane potential. Kir6.1, Kir6.2 and SUR2A were expressed in undifferentiated MSC, whereas SUR2B and SUR1 were not detected on cDNA and protein level. Upon adipogenic differentiation Kir6.1 and SUR2A showed a significant reduction of the amount of mRNA by 84% and 95%, respectively, whereas Kir6.2 expression was unchanged. Osteogenic differentiation strongly up-regulated Kir6.2 mRNA (28-fold) whereas Kir6.1 and SUR2A showed no significant change in expression. Quantitative Western blot analysis and immunofluorescence staining confirmed the elevated expression of Kir6.2 upon osteogenic differentiation. Taken together, expression changes of K(ATP) channels may contribute to in vitro differentiation of MSC and represent changes in the metabolic state of the developing tissue. Copyright Copyright 2011 Elsevier Ltd. All rights reserved.CAS Registry/EC Number/Name of Substance 0 (ATP-Binding Cassette Transporters). 0 (KATP Channels). 0 (Kir6.2 channel). 0 (Potassium Channels, Inwardly Rectifying). 0 (RNA, Messenger). 0 (Receptors, Drug). 0 (sulfonylurea receptor). 0 (uK-ATP-1 potassium channel).
机译:间充质基质细胞(MSC)在再生技术中的有希望的使用说明了对其生理学进行详细研究的必要性。专能细胞的增殖和分化通常涉及其代谢状态的变化。在本研究中,我们分析了MSC中以及体外分化后ATP敏感钾(K(ATP))通道的表达。 K(ATP)通道存在于许多细胞中,并通过使细胞代谢与膜电位耦合来调节多种细胞功能。 Kir6.1,Kir6.2和SUR2A在未分化的MSC中表达,而在基因和蛋白质水平上均未检测到SUR2B和SUR1。在成脂分化后,Kir6.1和SUR2A分别显示出mRNA量显着减少84%和95%,而Kir6.2表达未发生变化。成骨细胞分化强烈上调Kir6.2 mRNA(28倍),而Kir6.1和SUR2A在表达上没有明显变化。定量蛋白质印迹分析和免疫荧光染色证实了成骨细胞分化后Kir6.2的表达升高。综上所述,K(ATP)通道的表达变化可能有助于MSC的体外分化,并代表发育中组织的代谢状态变化。版权版权所有2011 ElsevierLtd。保留所有权利。CAS登记号/ EC编号/物质名称0(ATP盒式转运蛋白)。 0(KATP通道)。 0(Kir6.2通道)。 0(钾通道,向内整流)。 0(RNA,信使)。 0(受体,药物)。 0(磺酰脲受体)。 0(uK-ATP-1钾离子通道)。

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