Zhang Keqin, Barragan-Adjemian Cielo, Ye Ling, Kotha Shiva, Dallas Mark, Lu Yongbo, Zhao Shujie, Harris Marie, Harris Stephen E, Feng Jian Q, Bonewald Lynda F
Department of Oral Biology, School of Dentistry, University of Missouri at Kansas City, 630 East 25th Street, Kansas City, MO 64108-2784, USA.
Mol Cell Biol. 2006 Jun;26(12):4539-52. doi: 10.1128/MCB.02120-05.
Within mineralized bone, osteocytes form dendritic processes that travel through canaliculi to make contact with other osteocytes and cells on the bone surface. This three-dimensional syncytium is thought to be necessary to maintain viability, cell-to-cell communication, and mechanosensation. E11/gp38 is the earliest osteocyte-selective protein to be expressed as the osteoblast differentiates into an osteoid cell or osteocyte, first appearing on the forming dendritic processes of these cells. Bone extracts contain large amounts of E11, but immunostaining only shows its presence in early osteocytes compared to more deeply embedded cells, suggesting epitope masking by mineral. Freshly isolated primary osteoblasts are negative for E11 expression but begin to express this protein in culture, and expression increases with time, suggesting differentiation into the osteocyte phenotype. Osteoblast-like cell lines 2T3 and Oct-1 also show increased expression of E11 with differentiation and mineralization. E11 is highly expressed in MLO-Y4 osteocyte-like cells compared to osteoblast cell lines and primary osteoblasts. Differentiated, mineralized 2T3 cells and MLO-Y4 cells subjected to fluid flow shear stress show an increase in mRNA for E11. MLO-Y4 cells show an increase in dendricity and elongation of dendrites in response to shear stress that is blocked by small interfering RNA specific to E11. In vivo, E11 expression is also increased by a mechanical load, not only in osteocytes near the bone surface but also in osteocytes more deeply embedded in bone. Maximal expression is observed not in regions of maximal strain but in a region of potential bone remodeling, suggesting that dendrite elongation may be occurring during this process. These data suggest that osteocytes may be able to extend their cellular processes after embedment in mineralized matrix and have implications for osteocytic modification of their microenvironment.
在矿化骨中,骨细胞形成树突状突起,这些突起穿过骨小管与其他骨细胞及骨表面的细胞接触。这种三维合体被认为对于维持细胞活力、细胞间通讯和机械感知是必要的。E11/gp38是成骨细胞分化为类骨质细胞或骨细胞时最早表达的骨细胞选择性蛋白,最初出现在这些细胞正在形成的树突状突起上。骨提取物含有大量E11,但免疫染色显示,与更深层嵌入的细胞相比,它仅在早期骨细胞中存在,这表明其表位被矿物质掩盖。新鲜分离的原代成骨细胞E11表达呈阴性,但在培养过程中开始表达该蛋白,且表达随时间增加,这表明其分化为骨细胞表型。成骨样细胞系2T3和Oct-1在分化和矿化时E11表达也增加。与成骨细胞系和原代成骨细胞相比,E11在MLO-Y4骨细胞样细胞中高表达。分化的、矿化的2T3细胞和MLO-Y4细胞受到流体流动剪切应力作用时,E11的mRNA增加。MLO-Y4细胞对剪切应力的反应是树突增多和树突伸长,而这种反应被E11特异性小干扰RNA阻断。在体内,机械负荷也会增加E11的表达,不仅在骨表面附近的骨细胞中,在更深层嵌入骨中的骨细胞中也是如此。最大表达并非出现在应变最大的区域,而是出现在潜在骨重塑区域,这表明在此过程中可能发生树突伸长。这些数据表明,骨细胞在嵌入矿化基质后可能能够延伸其细胞突起,这对其微环境的骨细胞修饰具有重要意义。