About this Research Topic
A large literature exists on trabecular and cortical bone morphology. The engineering performance of bone, implied from its 3d architecture, is often the endpoint of bone biology experiments, being clinically relevant to bone fracture. How and why does bone travel along its complex spatio-temporal trajectory to acquire its architecture? The question “why” can have two meanings. The first, “teleological - why is an architecture advantageous?” – is the domain of substantial biomechanical research to date. The second, “etiological – how did an architecture come about?” – has received far less attention.
This Frontiers Bone Research topic welcomes contributions addressing this “etiological why” – what mechanisms can coordinate the activity of bone forming and resorbing cells to produce the observed complex and efficient bone architectures? One mechanism is proposed – chaotic nonlinear pattern formation (NPF) , , which underlies – in a unifying way – natural structures as disparate as trabecular bone, swarms of birds flying, island formation, fluid turbulence and others. At the heart of NPF is the fact that simple rules operating between interacting elements multiplied and repeated many times, lead to complex and structured patterns. This paradigm of growth and form leads to a profound link between bone regulation and its architecture: in bone the architecture is the regulation. The former is the emergent consequence of the latter.
What insights can the paradigm of NPF provide to bone biology? One example concerns the genetic disorder Juvenile Pagets Disease (JPD) or Idiopathic Hyperphosphatasia where the anomalous parallel trabecular architecture characteristic of this pathology is consistent with an NPF paradigm by analogy with known experimental NPF systems.
However there may equally be other mechanisms and insights into how bone acquires its architecture. Contributions are welcomed to explore such sources of the 4D pattern of bone.
Whatever mechanism does determine bone’s developing architecture has to operate at the level of individual sites of formation and resorption and coupling between the two. This has implications as to how we understand the effect on bone of agents such as gene products or drugs. It may be for instance that the “tuning” of coupling between formation and resorption might be as important as the achievement of enhanced bone volume.
Contributions are welcomed to look for ways in which this pattern-forming perspective might add to the understanding of phenomena of bone architechture observed clinically or experimentally.
Important Note: All contributions to this Research Topic must be within the scope of the section and journal to which they are submitted, as defined in their mission statements. Frontiers reserves the right to guide an out-of-scope manuscript to a more suitable section or journal at any stage of peer review.