Integrable models provide simplified examples of quantum field theories with self-interaction. As often in relativistic quantum theory, their local observables are difficult to control mathematically. One either tries to construct pointlike local quantum fields, leading to possibly divergent series expansions, or one defines the local observables indirectly via wedge-local quantities, losing control over their explicit form.

We propose a new, hybrid approach: We aim to describe local quantum fields; but rather than exhibiting their n-point functions and verifying the Wightman axioms, we establish them as closed operators affiliated with a net of von Neumann algebras. This is shown to work at least in the Ising model.

The renormalized expectation value of the stress energy tensor (RSET) is an object of central importance in quantum field theory in curved space-time, but calculating this on black hole space-times is far from trivial.  The vacuum polarization (VP) of a quantum scalar field is computationally simpler and shares some features with the RSET.  In this talk we consider the properties of the VP for a massless, conformally coupled scalar field on asymptotically anti-de Sitter black holes with spherical, flat and hyperbolic horizons.  We focus on the effect of the different horizon curvature on the VP, and the role played by the boundary conditions far from the black hole.     

I will review the idea that entanglement must ultimately be understood in terms of modes, rather than in terms of particles. The most striking instance of mode entanglement is a single particle entangled state, which I will discuss both in the case of bosons as well as in the case of fermions. I then proceed to show that the Aharonov-Bohm effect can be understood by using a single electron entangled state. Finally, I will argue that this demonstrates beyond doubt that the Aharonov-Bohm effect is non non-local, contrary to what is frequently claimed in the literature.

After reviewing our recent description of generalized Kahler structures in terms of holomorphic symplectic Morita equivalence, I will describe how this can be used for explicit constructions of toric generalized Kahler metrics.  Then I will describe how these ideas, combined with concepts from geometric quantization, provide a new approach to noncommutative algebraic geometry.

Mitral regurgitation is one of the most common valve diseases in the UK and contributes to 50% of the transcatheter mitral valve replacement (TMVR) procedures with bioprosthetic valves. TMVR is generally performed in frailer, older patients unlikely to tolerate open-heart surgery or further interventions. One of the side effects of implanting a bioprosthetic valve is a condition known as left ventricular outflow obstruction, whereby the implanted device can partially obstruct the outflow of blood from the left ventricle causing high flow resistance. The ventricle has then to pump more vigorously to provide adequate blood supply to the circulatory system and becomes hypertrophic. This ultimately results in poor contractility and heart failure.
We developed personalised image-based models to characterise the complex relationship between anatomy, blood flow, and ventricular function both before and after TMVR. The model prediction provides key information to match individual patient and device size, such as postoperative changes in intraventricular pressure gradients and blood residence time. Our pilot data from a cohort of 7 TMVR patients identified a correlation between the degree of outflow obstruction and the deterioration of ventricular function: when approximately one third of the outflow was obstructed as a result of the device implantation, significant increases in the flow resistance and the average time spent by the blood inside the ventricle were observed, which are in turn associated with hypertrophic ventricular remodelling and blood stagnation, respectively. Currently, preprocedural planning for TMVR relies largely on anecdotal experience and standard anatomical evaluations. The haemodynamic knowledge derived from the models has the potential to enhance significantly pre procedural planning and, in the long term, help develop a personalised risk scoring system specifically designed for TMVR patients.
 

Cellular migration can be affected by short-range interactions between cells such as volume exclusion, long-range forces such as chemotaxis, or reactions such as phenotypic switching. In this talk I will discuss how to incorporate these processes into a discrete or continuum modelling frameworks. In particular, we consider a system with two types of diffusing hard spheres that can react (switch type) upon colliding. We use the method of matched asymptotic expansions to obtain a systematic model reduction, consisting of a nonlinear reaction-diffusion system of equations. Finally, we demonstrate how this approach can be used to study the effects of excluded volume on cellular chemotaxis. This is joint work with Dan Wilson and Helen Byrne.
 

Mechanobiology is a field of science that aims to understand how mechanics regulate biology. It focuses on how mechanical forces and alterations in mechanical properties of cell or tissues regulate biological processes in development, physiology and disease. In fact, all these processes occur in our body, which presents a clear structural and hierarchical organization that goes from the organism to the cellular level. To advance in the understanding of all these processes at different scales requires the use of simplified representations of our body, which is normally known as modelling or equivalently the creation of a model. Different types of models can be found in the literature: in-vitro, in-vivo and in-silico models.

Here, I will present our modelling strategy in which we integrate different mathematical models and experiments in order to tackle relevant mechanical-based mechanisms in wound healing and cancer metastasis progression [1,2]. In fact, we have focused our research on individual [3] and collective cell migration [4], because it is a crucial event in all these mechanisms. Therefore, unravelling the intrinsic mechanisms that cells use to define their migration is an essential element for advancing the development of new technologies in regenerative medicine and cancer.

Due to the complexity of all these mechanisms, mathematical modelling is a relevant tool for providing deeper insight and quantitative predictions of the mechanical interplay between cells and extracellular matrix during cell migration. To assess the predictive capacity of these models, we will compare our numerical results with microfluidic-based experiments [2], which provide experimental information to test and refine the main assumptions of our models.

Actually, we design and fabricate multi-channel 3D microfluidics cell culture chips, which allow recreating the physiology and disease of one organ or any biological process with a precise control of the micro environmental factors [5]. Therefore, this kind of organ-on-a-chip experiments constitutes a novel modelling strategy of in vitro multicellular human systems that in combination with mathematical simulations provide a relevant tool for research in mechanobiology.

References

Escribano J, Chen M, Moeendarbary E, Cao X, Shenoy V, Garcia-Aznar JM, Kamm RD, Spill F.  Balance of Mechanical Forces Drives Endothelial Gap Formation and May Facilitate Cancer and Immune-Cell Extravasation. PLOS Computational Biology, in press.