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In an aging society where the number of joint replacements rises, it is important to also increase the longevity of implants.
In particular hip implants have a lifetime of at most 15 years. This derives primarily from
pain due to implant migration, wear, inflammation, and dislocation, which is affected by
the positioning of the implant during the surgery. Current joint replacement practice uses
2D software tools and relies on the experience of surgeons. Especially the 2D tools fail to
take the patients’ natural range of motion as well as stress distribution in the 3D joint
induced by different daily motions into account.
Optimizing the hip joint implant position for all possible parametrized motions under the
constraint of a contact problem is prohibitively expensive as there are too many motions
and every position change demands a recalculation of the contact problem. For the
reduction of the computational effort, we use adaptive refinement on the parameter
domain coupled with the interpolation method of Kriging. A coarse initial grid is to be
locally refined using goal-oriented error estimation, reducing locally high variances. This
approach will be combined with multi-grid optimization such that numerical errors are
reduced.
Following axon pathfinding, growth cones transition from stochastic filopodial exploration to the formation of a limited number of synapses. How the interplay of filopodia and synapse assembly ensures robust connectivity in the brain has remained a challenging problem. Here, we developed a new 4D analysis method for filopodial dynamics and a data-driven computational model of synapse formation for R7 photoreceptor axons in developing Drosophila brains. Our live data support a 'serial synapse formation' model, where at any time point only a single 'synaptogenic' filopodium suppresses the synaptic competence of other filopodia through competition for synaptic seeding factors. Loss of the synaptic seeding factors Syd-1 and Liprin-α leads to a loss of this suppression, filopodial destabilization and reduced synapse formation, which is sufficient to cause the destabilization of entire axon terminals. Our model provides a filopodial 'winner-takes-all' mechanism that ensures the formation of an appropriate number of synapses.