Jiang Jean X, Cherian Priscilla P
Department of Biochemistry, University of Texas Health Science Center, San Antonio, TX 78229, USA.
Cell Commun Adhes. 2003 Jul-Dec;10(4-6):259-64. doi: 10.1080/cac.10.4-6.259.264.
Osteocytes embedded in the matrix of bone are mechanosensory cells that translate strain into signals and regulate bone remodeling. Our previous studies using osteocyte-like MLO-Y4 cells have shown that fluid flow shear stress (FFSS) increases connexin (Cx) 43 protein expression, prostaglandin E(2) (PGE(2)) release, and intercellular coupling, and PGE(2) is an essential mediator between FFSS and gap junctions. However, the role of Cx43 in the release of PGE(2) in response to FFSS is unknown. Here, the FFSS-loaded MLO-Y4 cells with no or few intercellular channels released significantly more PGE(2) per cell than those cells at higher densities. Antisense Cx43 oligonucleotides and 18 beta-glycyrrhetinic acid, a specific gap junction and hemichannel blocker, significantly reduced PGE(2) release by FFSS at all cell densities tested, especially cells at the lowest density without gap junctions. FFSS, fluid flow-conditioned medium, and PGE(2) increased the activity of dye uptake. Moreover, FFSS induced Cx43 to migrate to the surface of the cell; this surface expressed Cx43 developed resistance to Triton-X-100 solublization. Our results suggest that hemichannels formed by Cx43, instead of intercellular channels, are likely to play a predominant role in the release of intracellular PGE(2) in response to FFSS.
嵌入骨基质中的骨细胞是机械感觉细胞,可将应变转化为信号并调节骨重塑。我们之前使用类骨细胞MLO-Y4细胞进行的研究表明,流体流动剪切应力(FFSS)可增加连接蛋白(Cx)43的蛋白表达、前列腺素E(2)(PGE(2))的释放以及细胞间偶联,并且PGE(2)是FFSS与间隙连接之间的重要介质。然而,Cx43在响应FFSS时PGE(2)释放中的作用尚不清楚。在此,与细胞间通道极少或没有的FFSS加载的MLO-Y4细胞相比,高密度的那些细胞每个细胞释放的PGE(2)明显更多。反义Cx43寡核苷酸和18β-甘草次酸(一种特异性间隙连接和半通道阻滞剂)在所有测试的细胞密度下均显著降低了FFSS诱导的PGE(2)释放,尤其是在没有间隙连接的最低密度细胞中。FFSS、流体流动条件培养基和PGE(2)增加了染料摄取活性。此外,FFSS诱导Cx43迁移至细胞表面;这种表面表达的Cx43对Triton-X-100溶解产生抗性。我们的结果表明,由Cx43形成的半通道而非细胞间通道可能在响应FFSS时细胞内PGE(2)的释放中起主要作用。