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Functionally improved bone in Calbindin-D28k knockout mice

机译:Calbindin-D28k基因敲除小鼠的骨骼功能改善

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摘要

In vitro studies indicate that Calbindin-D28k, a calcium binding protein, is important in regulating the life span of osteoblasts as well as the mineralization of bone extracellular matrix. The recent creation of a Calbindin-D28k knockout mouse has provided the opportunity to study the physiological effects of the Calbindin-D28k protein on bone remodeling in vivo. In this experiment, histomorphometry, μCT, and bend testing were used to characterize bones in Calbindin-D28k KO (knockout) mice. The femora of Calbindin-D28k KO mice had significantly increased cortical bone volume (60.4% ± 3.1) compared to wild-type (WT) mice (45.4% ± 4.6). The increased bone volume was due to a decrease in marrow cavity area, and significantly decreased endosteal perimeters (3.397 mm ± 0.278 in Calbindin-D28k KO mice, and 4.046 mm ± 0.450 in WT mice). Similar changes were noted in the analysis of the tibias in both mice. The bone formation rates were similar in the femoral and tibial cortical bones of both mice. μCT analysis of the trabecular bone in the tibial plateau indicated that Calbindin-D28k KO mice had an increased bone volume (35.2% ± 3.1) compared to WT mice (24.7% ± 4.9) which was primarily due to increased trabecular number (8.99 mm−1 ± 0.94 in Calbindin-D28k KO mice compared to 6.75 mm−1 ± 0.85 in WT mice). Bone mineral content analysis of the tibias indicated that there is no difference in the calcium or phosphorus content between the Calbindin-D28k KO and WT mice. Cantilever bend testing of the femora demonstrated significantly lower strains in the bones of Calbindin-D28k KO mice (4135 μstrain/kg ± 1266) compared to WT mice (6973 μstrain/kg ± 998) indicating that the KO mice had stiffer bones. Three-point bending demonstrated increased failure loads in bones of Calbindin-D28k KO mice (31.6 N ± 2.1) compared to WT mice (15.0 N ± 1.7). In conclusion, Calbindin-D28k KO mice had increased bone volume and stiffness indicating that Calbindin-D28k plays an important role in bone remodeling.
机译:体外研究表明,钙结合蛋白Calbindin-D28k在调节成骨细胞的寿命以及骨细胞外基质的矿化中很重要。 Calbindin-D28k基因敲除小鼠的最新创建提供了研究Calbindin-D28k蛋白对体内骨重塑的生理作用的机会。在该实验中,使用组织形态计量学,μCT和弯曲测试来表征Calbindin-D28k KO(敲除)小鼠的骨骼。与野生型(WT)小鼠(45.4%±4.6)相比,Calbindin-D28k KO小鼠的股骨皮层骨体积显着增加(60.4%±3.1)。骨量的增加是由于骨髓腔面积的减少,以及骨内膜周长的明显减少(Calbindin-D28k KO小鼠为3.397 mm±0.278,WT小鼠为4.046 mm±0.450)。在两只小鼠的胫骨分析中都注意到了类似的变化。两只小鼠的股骨和胫骨皮质骨的骨形成率相似。胫骨平台小梁骨的μCT分析表明,与WT小鼠(24.7%±4.9)相比,Calbindin-D28k KO小鼠的骨体积增加(35.2%±3.1),这主要是由于小梁骨数目增加(8.99 mm < Calbindin-D28k KO小鼠中sup> -1 ±0.94,而WT小鼠中则为6.75 mm -1 ±0.85)。胫骨的骨矿物质含量分析表明,Calbindin-D28k KO和WT小鼠之间的钙或磷含量没有差异。股骨的悬臂弯曲测试显示,与WT小鼠(6973μstrain/ kg±998)相比,Calbindin-D28k KO小鼠的骨骼应变显着降低(4135μs/ kg±1266),表明KO小鼠的骨骼较硬。与WT小鼠(15.0 N±1.7)相比,三点弯曲证明了Calbindin-D28k KO小鼠(31.6 N±2.1)的骨骼中增加的破坏负荷。总之,Calbindin-D28k KO小鼠的骨体积和僵硬度增加,表明Calbindin-D28k在骨骼重塑中起重要作用。

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