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Biology subjects

Meuris, B.

Publications and source records attributed to Meuris, B..

2 recordsLinked to original sources

Feasibility study of fluid-structure-growth modelling in the context of endogenous tissue restoration

In situ tissue engineering exploits natural inflammatory responses to turn a synthetic vascular graft into a regenerated, functioning, and living vessel through endogenous tissue restoration. Despite promising preclinical results, challenges remain, especially in high-pressure regimes. To better understand the underlying biological processes and predict long-term outcomes of graft implantation, we propose an in silico approach. We account for the solid mechanics of conduit grafts in high and low pressure regimes, the wall shear stresses, and long-term growth and remodeling through two reduced-order fluid-structure-growth models. The first employs an artificial neural network surrogate model to compute the time-averaged wall shear stress at every growth step, whereas the second evaluates a fully-coupled fluid-structure interaction model every 60 time steps. We thoroughly verify both models and confirm acceptable model-form errors, then calibrate them against data from animal experiments. A validation study comparing in silico predictions with unseen animal data of carotid and pulmonary conduit grafts confirms that the model remains reliable up to at least one month of prediction time, hence in the future enabling in silico optimization of short-term endogenous tissue restoration in tissue engineering vascular grafts.

bioengineering↗

Cross-species proteomics quantification pipeline distinguishes donor versus host extracellular matrix in explanted biomaterials

Xenogenic biomaterial durability, including bioprosthetic heart valves (BPVs), is compromised by pathological extracellular matrix (ECM) remodeling, resulting in progressive structural degeneration. Mass spectrometry-based proteomics can help reveal BPV degeneration mechanisms; however, peptide sequence similarity between donor and host species complicates protein-level analysis. We present a cross-species proteomic analytical strategy for xenogenic biomaterials and cross-species proteomic datasets. In silico tryptic digestion of human and bovine protein databases identified over 400 overlapping proteins with a high protein percent identity. Explanted human BPV tissue was divided into macroscopically distinct regions of degeneration and analyzed by mass spectrometry. A peptide-level strategy quantified protein abundances in a species-delineated analysis. We highlighted degeneration region-specific depositions of key human ECM proteins and bovine ECM proteins whose abundance is time dependent. We demonstrated that single-species analysis of a cross-species proteome results in inaccurate quantification. This study highlights the importance of distinguishing between donor and host species proteomes for accurate protein quantification. While focused on clinically explanted biomaterials, our approach is broadly applicable to all forms of xenotransplantation and the use of xenogenic matrices.

bioengineering↗