Journal
CELLULAR AND MOLECULAR LIFE SCIENCES
Volume 78, Issue 15, Pages 5755-5773Publisher
SPRINGER BASEL AG
DOI: 10.1007/s00018-021-03884-w
Keywords
Cortical bone; Cortical porosity; Bone strength; Bone growth; sFRP4; Notum
Categories
Funding
- Mochida Memorial Foundation for Medical and Pharmacological Research
- The Foundation for Growth Science, Japan
- NHMRC Senior Research Fellowship
- Victorian State Government's Operational Infrastructure Support program
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The article discusses the mechanisms of cortical bone development, growth, and degeneration, as well as genetic modifications and sex-specific differences. With aging, the process of consolidation reverses, leading to cortical porosity and loss of bone strength. These processes require coordination between cell-specific signaling pathways.
Cortical bone structure is a crucial determinant of bone strength, yet for many years studies of novel genes and cell signalling pathways regulating bone strength have focused on the control of trabecular bone mass. Here we focus on mechanisms responsible for cortical bone development, growth, and degeneration, and describe some recently described genetic-driven modifications in humans and mice that reveal how these processes may be controlled. We start with embryonic osteogenesis of preliminary bone structures preceding the cortex and describe how this structure consolidates then matures to a dense, vascularised cortex containing an increasing proportion of lamellar bone. These processes include modelling-induced, and load-dependent, asymmetric cortical expansion, which enables the cortex's transition from a highly porous woven structure to a consolidated and thickened highly mineralised lamellar bone structure, infiltrated by vascular channels. Sex-specific differences emerge during this process. With aging, the process of consolidation reverses: cortical pores enlarge, leading to greater cortical porosity, trabecularisation and loss of bone strength. Each process requires co-ordination between bone formation, bone mineralisation, vascularisation, and bone resorption, with a need for locational-, spatial- and cell-specific signalling pathways to mediate this co-ordination. We will discuss these processes, and a number of cell-signalling pathways identified in both murine and human genetic studies to regulate cortical bone mass, including signalling through gp130, STAT3, PTHR1, WNT16, NOTCH, NOTUM and sFRP4.
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