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振荡流体流动通过ERK1/2丝裂原活化蛋白激酶依赖性机制调节骨细胞MLO-Y4细胞中的间隙连接通讯。

Oscillating fluid flow regulates gap junction communication in osteocytic MLO-Y4 cells by an ERK1/2 MAP kinase-dependent mechanism.

作者信息

Alford A I, Jacobs C R, Donahue H J

机构信息

Department of Orthopedics and Rehabilitation, The Pennsylvania State University College of Medicine, Hershey, PA 17033, USA.

出版信息

Bone. 2003 Jul;33(1):64-70. doi: 10.1016/s8756-3282(03)00167-4.

Abstract

The present work was designed to investigate the effects of oscillating fluid flow on gap junctional intercellular communication (GJIC) and the gap junction protein connexin (Cx) 43 in osteocyte-like MLOY-4 cells. Cells were exposed for 1 h to oscillating fluid flow at a shear stress of +/-10 dyn/cm(2) and a frequency of 1 Hz in a parallel plate flow chamber. Control cells were incubated in the chamber but were not exposed to oscillating fluid flow. Functional analysis of GJIC indicated that MLOY-4 cells exposed to oscillating fluid flow established more gap junctions with an independent population of dye-labeled cells than did control cells. Phosphorylation of Cx43 was quantified by immunoprecipitation with an anti-Cx43 antibody followed by immunoblot analysis using an anti-phosphoserine antibody. Phosphoserine was normalized to Cx43 in each sample. Compared to control cells, phosphoserine content of Cx43 increased approximately twofold in cells exposed to oscillating fluid flow. The possible role of the extracellular signal regulated kinase (ERK1/2) in the flow-induced upregulation of GJIC was also investigated. The ERK1/2 inhibitor PD-98059 significantly attenuated the effects of oscillating fluid flow on MLOY-4 cells GJIC. These results indicate that oscillating fluid flow regulates GJIC in MLOY-4 cells via the ERK1/2 MAP kinase. In addition, increased serine phosphorylation of Cx43 correlates with the flow-induced increase in GJIC.

摘要

本研究旨在探讨振荡流体流动对骨细胞样MLOY-4细胞间隙连接细胞间通讯(GJIC)及间隙连接蛋白连接蛋白(Cx)43的影响。将细胞在平行板流动腔中暴露于剪切应力为+/-10达因/平方厘米、频率为1赫兹的振荡流体流动1小时。对照细胞在腔中孵育,但未暴露于振荡流体流动。GJIC的功能分析表明,与对照细胞相比,暴露于振荡流体流动的MLOY-4细胞与独立的染料标记细胞群体建立了更多的间隙连接。通过用抗Cx43抗体进行免疫沉淀,然后使用抗磷酸丝氨酸抗体进行免疫印迹分析来定量Cx43的磷酸化。将每个样品中的磷酸丝氨酸标准化为Cx43。与对照细胞相比,暴露于振荡流体流动的细胞中Cx43的磷酸丝氨酸含量增加了约两倍。还研究了细胞外信号调节激酶(ERK1/2)在流动诱导的GJIC上调中的可能作用。ERK1/2抑制剂PD-98059显著减弱了振荡流体流动对MLOY-4细胞GJIC的影响。这些结果表明,振荡流体流动通过ERK1/2丝裂原活化蛋白激酶调节MLOY-4细胞中的GJIC。此外,Cx43丝氨酸磷酸化增加与流动诱导的GJIC增加相关。

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