Miyazaki Shihoko, Funamoto Taro, Sekimoto Tomohisa, Kurogi Syuji, Ohta Tomomi, Nagai Takuya, Tajima Takuya, Imasaka Mai, Yoshinobu Kumiko, Araki Kimi, Araki Masatake, Choijookhuu Narantsog, Hishikawa Yoshitaka, Chosa Etsuo
Division of Orthopaedic Surgery, Department of Medicine of Sensory and Motor Organs, Faculty of Medicine, University of Miyazaki, Japan.
Department of Genetics, Hyogo College of Medicine, Japan.
Acta Histochem Cytochem. 2022 Jun 29;55(3):99-110. doi: 10.1267/ahc.22-00027. Epub 2022 Jun 25.
Epithelial protein lost in neoplasm (EPLIN) is an actin-associated cytoskeletal protein that plays an important role in epithelial cell adhesion. EPLIN has two isoforms: EPLINα and EPLINβ. In this study, we investigated the role of EPLINβ in osteoblasts using EPLINβ-deficient ( ) mice. The skeletal phenotype of mice is indistinguishable from the wildtype (WT), but bone properties and strength were significantly decreased compared with WT littermates. Histomorphological analysis revealed altered organization of bone spicules and osteoblast cell arrangement, and decreased alkaline phosphatase activity in mouse bones. Transmission electron microscopy revealed wider intercellular spaces between osteoblasts in mice, suggesting aberrant cell adhesion. In osteoblasts, α- and β-catenins and F-actin were observed at the cell membrane, but OB-cadherin was localized at the perinuclear region, indicating that cadherin-catenin complexes were not formed. EPLINβ knockdown in MC3T3-e1 osteoblast cells showed similar results as in calvaria cell cultures. Bone formation markers, such as , , , and mRNA were reduced in EPLINβ knockdown cells, suggesting an important role for EPLINβ in osteoblast formation. In conclusion, we propose that EPLINβ is involved in the assembly of cadherin-catenin complexes in osteoblasts and affects bone formation.
肿瘤中丢失的上皮蛋白(EPLIN)是一种与肌动蛋白相关的细胞骨架蛋白,在上皮细胞黏附中起重要作用。EPLIN有两种异构体:EPLINα和EPLINβ。在本研究中,我们使用EPLINβ缺陷型小鼠研究了EPLINβ在成骨细胞中的作用。EPLINβ缺陷型小鼠的骨骼表型与野生型(WT)小鼠无法区分,但与野生型同窝小鼠相比,其骨特性和强度显著降低。组织形态学分析显示,EPLINβ缺陷型小鼠骨小梁的组织结构和成骨细胞排列发生改变,且骨碱性磷酸酶活性降低。透射电子显微镜显示,EPLINβ缺陷型小鼠成骨细胞之间的细胞间隙更宽,提示细胞黏附异常。在EPLINβ缺陷型成骨细胞中,α-连环蛋白、β-连环蛋白和F-肌动蛋白在细胞膜上可见,但OB-钙黏蛋白定位于核周区域,表明钙黏蛋白-连环蛋白复合物未形成。在MC3T3-e1成骨细胞中敲低EPLINβ的结果与颅骨细胞培养中的结果相似。在敲低EPLINβ的细胞中,骨形成标志物如 、 、 和 的mRNA水平降低,提示EPLINβ在成骨细胞形成中起重要作用。总之,我们认为EPLINβ参与成骨细胞中钙黏蛋白-连环蛋白复合物的组装并影响骨形成。