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Transient Overexpression of Sonic Hedgehog Alters the Architecture and Mechanical Properties of Trabecular Bone

机译:瞬态超音速刺猬改变小梁骨的体系结构和力学性能

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摘要

Bone formation and remodeling involve coordinated interactions between osteoblasts and osteoclasts through signaling networks involving a variety of molecular pathways. We hypothesized that overexpression of Sonic hedgehog (Shh), a morphogen with a crucial role in skeletal development, would stimulate osteoblastogenesis and bone formation in adult animals in vivo. Systemic administration of adenovirus expressing the N-terminal form of Shh into adult mice resulted in a primary increase in osteoblasts and their precursors. Surprisingly, however, this was associated with altered trabecular morphology, decreased bone volume, and decreased compressive strength in the vertebrae. Whereas no change was detected in the number of osteoclast precursors, bone marrow stromal cells from Shh-treated mice showed enhanced osteoclastogenic potential in vitro. These effects were mediated by the PTH/PTH-related protein (PTHrP) pathway as evidenced by increased sensitivity to PTH stimulation and upregulation of the PTH/PTHrP receptor (PPR). Together, these data show that Shh has stimulatory effects on osteoprogenitors and osteoblasts in adult animals in vivo, which results in bone remodeling and reduced bone strength because of a secondary increase in osteoclastogenesis.
机译:骨形成和重塑涉及成骨细胞和破骨细胞之间通过涉及各种分子途径的信号网络的协同相互作用。我们假设超表达声波刺猬(Shh),一种在骨骼发育中起关键作用的形态发生子,会刺激成年动物体内成骨细胞的生成和骨骼的形成。将成年小鼠表达Shh的N末端形式的腺病毒的系统管理导致成骨细胞及其前体的主要增加。然而,令人惊讶的是,这与小梁的形态改变,骨量减少以及椎骨的抗压强度降低有关。尽管破骨细胞前体的数量未见变化,但经Shh处理的小鼠的骨髓基质细胞在体外显示出增强的破骨细胞潜力。这些作用由PTH / PTH相关蛋白(PTHrP)途径介导,对PTH刺激的敏感性增加和PTH / PTHrP受体(PPR)的上调证明了这一点。总之,这些数据表明Shh在体内对成年动物的骨祖细胞和成骨细胞具有刺激作用,由于破骨细胞生成的继发性增加,导致骨重塑和骨强度降低。

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