EPLINβ Is Involved in the Assembly of Cadherin-catenin Complexes in Osteoblasts and Affects Bone Formation.

IF 1.6 4区 生物学 Q4 CELL BIOLOGY
Acta Histochemica Et Cytochemica Pub Date : 2022-06-29 Epub Date: 2022-06-25 DOI:10.1267/ahc.22-00027
Shihoko Miyazaki, Taro Funamoto, Tomohisa Sekimoto, Syuji Kurogi, Tomomi Ohta, Takuya Nagai, Takuya Tajima, Mai Imasaka, Kumiko Yoshinobu, Kimi Araki, Masatake Araki, Narantsog Choijookhuu, Yoshitaka Hishikawa, Etsuo Chosa
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引用次数: 2

Abstract

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 (EPLINβGT/GT ) mice. The skeletal phenotype of EPLINβGT/GT 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 EPLINβGT/GT mouse bones. Transmission electron microscopy revealed wider intercellular spaces between osteoblasts in EPLINβGT/GT mice, suggesting aberrant cell adhesion. In EPLINβGT/GT 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 RUNX2, Osterix, ALP, and Col1a1 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.

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EPLINβ参与成骨细胞钙粘蛋白-连环蛋白复合物的组装并影响骨形成
肿瘤上皮蛋白丢失(EPLIN)是一种肌动蛋白相关的细胞骨架蛋白,在上皮细胞粘附中起重要作用。EPLIN有两个亚型:EPLINα和EPLINβ。在这项研究中,我们利用EPLINβ-缺陷(EPLINβGT/GT)小鼠研究了EPLINβ在成骨细胞中的作用。EPLINβGT/GT小鼠的骨骼表型与野生型(WT)没有区别,但骨性能和强度与野生型(WT)相比显著降低。组织形态学分析显示EPLINβGT/GT小鼠骨的骨针组织和成骨细胞排列发生改变,碱性磷酸酶活性降低。透射电镜显示EPLINβGT/GT小鼠成骨细胞间细胞间隙变宽,提示细胞粘附异常。在EPLINβGT/GT成骨细胞中,细胞膜上可见α-、β-连环蛋白和f -肌动蛋白,OB-cadherin定位于核周区域,说明没有形成cadherin-catenin复合物。在MC3T3-e1成骨细胞中,EPLINβ敲低的结果与颅骨细胞培养的结果相似。骨形成标志物,如RUNX2、Osterix、ALP和Col1a1 mRNA在EPLINβ敲低的细胞中减少,表明EPLINβ在成骨细胞形成中起重要作用。综上所述,我们认为EPLINβ参与了成骨细胞中钙粘蛋白-连环蛋白复合物的组装并影响骨的形成。
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来源期刊
Acta Histochemica Et Cytochemica
Acta Histochemica Et Cytochemica 生物-细胞生物学
CiteScore
3.50
自引率
8.30%
发文量
17
审稿时长
>12 weeks
期刊介绍: Acta Histochemica et Cytochemica is the official online journal of the Japan Society of Histochemistry and Cytochemistry. It is intended primarily for rapid publication of concise, original articles in the fields of histochemistry and cytochemistry. Manuscripts oriented towards methodological subjects that contain significant technical advances in these fields are also welcome. Manuscripts in English are accepted from investigators in any country, whether or not they are members of the Japan Society of Histochemistry and Cytochemistry. Manuscripts should be original work that has not been previously published and is not being considered for publication elsewhere, with the exception of abstracts. Manuscripts with essentially the same content as a paper that has been published or accepted, or is under consideration for publication, will not be considered. All submitted papers will be peer-reviewed by at least two referees selected by an appropriate Associate Editor. Acceptance is based on scientific significance, originality, and clarity. When required, a revised manuscript should be submitted within 3 months, otherwise it will be considered to be a new submission. The Editor-in-Chief will make all final decisions regarding acceptance.
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