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骨膜:生物学、调节机制及对骨质疏松症治疗的反应

Periosteum: biology, regulation, and response to osteoporosis therapies.

作者信息

Allen Matthew R, Hock Janet M, Burr David B

机构信息

Department of Anatomy and Cell Biology, Indiana University School of Medicine, Indianapolis, IN 46202, USA.

出版信息

Bone. 2004 Nov;35(5):1003-12. doi: 10.1016/j.bone.2004.07.014.

Abstract

Periosteum contains osteogenic cells that regulate the outer shape of bone and work in coordination with inner cortical endosteum to regulate cortical thickness and the size and position of a bone in space. Induction of periosteal expansion, especially at sites such as the lumbar spine and femoral neck, reduces fracture risk by modifying bone dimensions to increase bone strength. The cell and molecular mechanisms that selectively and specifically activate periosteal expansion, as well as the mechanisms by which osteoporosis drugs regulate periosteum, remain poorly understood. We speculate that an alternate strategy to protect human bones from fracture may be through targeting of the periosteum, either using current or novel agents. In this review, we highlight current concepts of periosteal cell biology, including their apparent differences from endosteal osteogenic cells, discuss the limited data regarding how the periosteal surface is regulated by currently approved osteoporosis drugs, and suggest one potential means through which targeting periosteum may be achieved. Improving our understanding of mechanisms controlling periosteal expansion will likely provide insights necessary to enhance current and develop novel interventions to further reduce the risk of osteoporotic fractures.

摘要

骨膜含有成骨细胞,这些细胞调节骨的外部形状,并与内部皮质骨内膜协同作用,以调节皮质厚度以及骨在空间中的大小和位置。诱导骨膜扩张,尤其是在腰椎和股骨颈等部位,通过改变骨尺寸以增加骨强度来降低骨折风险。选择性且特异性激活骨膜扩张的细胞和分子机制,以及骨质疏松症药物调节骨膜的机制,仍知之甚少。我们推测,保护人类骨骼免受骨折的另一种策略可能是通过使用现有或新型药物靶向骨膜。在本综述中,我们强调了骨膜细胞生物学的当前概念,包括它们与骨内膜成骨细胞的明显差异,讨论了关于目前批准的骨质疏松症药物如何调节骨膜表面的有限数据,并提出了一种可能实现靶向骨膜的潜在方法。增进我们对控制骨膜扩张机制的理解,可能会为加强现有干预措施和开发新的干预措施以进一步降低骨质疏松性骨折风险提供必要的见解。

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