Departments of Pathology, Anatomy and Laboratory Medicine, and of Microbiology, Immunology & Cell Biology, West Virginia University School of Medicine, Morgantown, WV, United States of America.
Fels Cancer Institute for Personalized Medicine, Department of Cancer and Cellular Biology, Lewis Katz School of Medicine at Temple University, Philadelphia, PA, United States of America.
PLoS One. 2023 May 11;18(5):e0264596. doi: 10.1371/journal.pone.0264596. eCollection 2023.
The calcium-selective ion channel Orai1 has a complex role in bone homeostasis, with defects in both bone production and resorption detected in Orai1 germline knock-out mice. To determine whether Orai1 has a direct, cell-intrinsic role in osteoblast differentiation and function, we bred Orai1 flox/flox (Orai1fl/fl) mice with Runx2-cre mice to eliminate its expression in osteoprogenitor cells. Interestingly, Orai1 was expressed in a mosaic pattern in Orai1fl/fl-Runx2-cre bone. Specifically, antibody labeling for Orai1 in vertebral sections was uniform in wild type animals, but patchy regions in Orai1fl/fl-Runx2-cre bone revealed Orai1 loss while in other areas expression persisted. Nevertheless, by micro-CT, bones from Orai1fl/fl-Runx2-cre mice showed reduced bone mass overall, with impaired bone formation identified by dynamic histomorphometry. Cortical surfaces of Orai1fl/fl-Runx2-cre vertebrae however exhibited patchy defects. In cell culture, Orai1-negative osteoblasts showed profound reductions in store-operated Ca2+ entry, exhibited greatly decreased alkaline phosphatase activity, and had markedly impaired substrate mineralization. We conclude that defective bone formation observed in the absence of Orai1 reflects an intrinsic role for Orai1 in differentiating osteoblasts.
钙选择性离子通道 Orai1 在骨稳态中具有复杂的作用,在 Orai1 种系敲除小鼠中检测到骨生成和吸收的缺陷。为了确定 Orai1 在成骨细胞分化和功能中是否具有直接的、细胞内固有作用,我们将 Orai1 flox/flox(Orai1fl/fl)小鼠与 Runx2-cre 小鼠杂交,以消除其在成骨前体细胞中的表达。有趣的是,Orai1 在 Orai1fl/fl-Runx2-cre 骨中以镶嵌模式表达。具体来说,在野生型动物中,Orai1 在椎骨切片中的抗体标记是均匀的,但在 Orai1fl/fl-Runx2-cre 骨的斑驳区域中,Orai1 的表达丢失,而在其他区域则持续存在。尽管如此,通过 micro-CT,Orai1fl/fl-Runx2-cre 小鼠的骨骼总体上显示出骨量减少,通过动态组织形态计量学鉴定出骨形成受损。然而,Orai1fl/fl-Runx2-cre 椎骨的皮质表面表现出斑驳的缺陷。在细胞培养中,Orai1 阴性成骨细胞的储存操作钙内流显著减少,碱性磷酸酶活性大大降低,基质矿化明显受损。我们得出结论,Orai1 缺失观察到的骨形成缺陷反映了 Orai1 在分化成骨细胞中的内在作用。