Thi Mia M, Kojima Takashi, Cowin Stephen C, Weinbaum Sheldon, Spray David C
New York Center for Biomedical Engineering, City College of the City University of New York, New York, 10031, USA.
Am J Physiol Cell Physiol. 2003 Feb;284(2):C389-403. doi: 10.1152/ajpcell.00052.2002. Epub 2002 Oct 3.
We tested the hypothesis that fluid shear stress (tau) modifies the expression, function, and distribution of junctional proteins [connexin (Cx)43, Cx45, and zona occludens (ZO)-1] in cultured bone cells. Cell lines with osteoblastic (MC3T3-E1 cells) and osteocytic (MLO-Y4 cells) phenotypes were exposed to tau-values of 5 or 20 dyn/cm(2) for 1-3 h. Immunostaining indicated that at 5 dyn/cm(2), the distribution of Cx43, Cx45, and ZO-1 was moderately disrupted at cell membranes; at 20 dyn/cm(2), disruption was more severe. Intercellular coupling was significantly decreased at both shear stress levels. Western blots showed the downregulation of membrane-bound Cx43 and ZO-1 and the upregulation of cytosolic Cx43 and Cx45 at different levels of shear stress. Similarly, Northern blots revealed that expression of Cx43, Cx45, and ZO-1 was selectively up- and downregulated in response to different shear stress levels. These results indicate that in cultured bone cells, fluid shear stress disrupts junctional communication, rearranges junctional proteins, and determines de novo synthesis of specific connexins to an extent that depends on the magnitude of the shear stress. Such disconnection from the bone cell network may provide part of the signal whereby the disconnected cells or the remaining network initiate focal bone remodeling.
流体剪切应力(τ)可改变培养骨细胞中连接蛋白(连接蛋白(Cx)43、Cx45和闭合蛋白(ZO)-1)的表达、功能及分布。将具有成骨细胞(MC3T3-E1细胞)和骨细胞(MLO-Y4细胞)表型的细胞系暴露于5或20达因/平方厘米的τ值下1至3小时。免疫染色表明,在5达因/平方厘米时,Cx43、Cx45和ZO-1在细胞膜处的分布受到中度破坏;在20达因/平方厘米时,破坏更为严重。在这两种剪切应力水平下,细胞间偶联均显著降低。蛋白质免疫印迹显示,在不同水平的剪切应力下,膜结合的Cx43和ZO-1下调,而胞质中的Cx43和Cx45上调。同样,RNA印迹显示,Cx43、Cx45和ZO-1的表达响应不同的剪切应力水平而选择性地上调或下调。这些结果表明,在培养的骨细胞中,流体剪切应力会破坏连接通讯、重新排列连接蛋白,并在一定程度上决定特定连接蛋白的从头合成,这取决于剪切应力的大小。与骨细胞网络的这种断开连接可能提供了部分信号,借此断开连接的细胞或剩余网络启动局部骨重塑。