Development of PLGA-coated β-TCP scaffolds containing VEGF for bone tissue engineering

Bone tissue engineering is sought to apply strategies for bone defects healing without limitations and short-comings of using either bone autografts or allografts and xenografts. The aim of this study was to fabricate a thin layer poly(lactic-co-glycolic) acid (PLGA) coated beta-tricalcium phosphate (β-TCP) scaffold with sustained release of vascular endothelial growth factor (VEGF). PLGA coating increased compressive strength of the β-TCP scaffolds significantly. For in vitro evaluations, canine mesenchymal stem cells (cMSCs) and canine endothelial progenitor cells (cEPCs) were isolated and characterized. Cell proliferation and attachment were demonstrated and the rate of cells proliferation on the VEGF released scaffold was significantly more than compared to the scaffolds with no VEGF loading. A significant increase in expression of COL1 and RUNX2 was indicated in the scaffolds loaded with VEGF and MSCs compared to the other groups. Consequently, PLGA coated β-TCP scaffold with sustained and localized release of VEGF showed favourable results for bone regeneration in vitro, and this scaffold has the potential to use as a drug delivery device in the future

A new model of passive muscle tissue integrating Collagen Fibers: Consequences for muscle behavior analysis

International audienceMechanical properties of muscle tissue are crucial in biomechanical modeling of the human body. Muscle tissue is a combination of Muscle Fibers (MFs) and connective tissue including collagen and elastin fibers. There are a lot of passive muscle models in the literature but most of them do not consider any distinction between Collagen Fibers (CFs) and MFs, or at least do not consider the mechanical effects of the CFs on the Three-Dimensional (3-D) behavior of tissue. As a consequence, unfortunately, they cannot describe the observed stress-stretch behavior in tissue in which the reinforced direction is not parallel to the MF direction. In this research, a new passive muscle model is presented, in which the CFs are separately considered in the formulation: they are distributed along the MFs in a cross-shaped arrangement. Thanks to this new architecture, a mechanical reinforced direction can be proposed, in addition to the muscle main fiber direction.The passive biomechanical properties of the genioglossus muscle of a bovine tongue have been measured under uniaxial tensile tests. To characterize the 3-D response of the tissue, tests have been performed in different directions with respect to the MF direction. Moreover, a Constitutive Law (CL) has been proposed for modeling this behavior. In addition to our measurements on the bovine genioglossus muscle, results published in the literature on experimental data from the longissimus dorsi of pigs and the chicken pectoralis muscle were used to appraise the applicability of the proposed model. It is demonstrated that the proposed passive muscle model provides an accurate description of the fiber-oriented nature of muscle tissue. Also, it has been shown that using Finite Element Analysis (FEA) it might be possible to predict the angle θ between CFs and MF

A visco-hyperelastic constitutive model and its application in bovine tongue tissue

International audienceMaterial properties of the human tongue tissue have a significant role in understanding its function in speech, respiration, suckling, and swallowing. Tongue as a combination of various muscles is surrounded by the mucous membrane and is a complicated architecture to study. As a first step before the quantitative mechanical characterization of human tongue tissues, the passive biomechanical properties in the superior longitudinal muscle (SLM) and the mucous tissues of a bovine tongue have been measured. Since the rate of loading has a sizeable contribution to the resultant stress of soft tissues, the rate dependent behavior of tongue tissues has been investigated via uniaxial tension tests (UTTs). A method to determine the mechanical properties of transversely isotropic tissues using UTTs and inverse finite element (FE) method has been proposed. Assuming the strain energy as a general nonlinear relationship with respect to the stretch and the rate of stretch, two visco-hyperelastic constitutive laws (CLs) have been proposed for isotropic and transversely isotropic soft tissues to model their stress-stretch behavior. Both of them have been implemented in ABAQUS explicit through coding a user-defined material subroutine called VUMAT and the experimental stress-stretch points have been well tracked by the results of FE analyses. It has been demonstrated that the proposed laws make a good description of the viscous nature of tongue tissues. Reliability of the proposed models has been compared with similar nonlinear visco-hyperelastic CLs

Atomic Force Microscopy Stiffness Mapping in Human Aortic Smooth Muscle Cells

International audienceAortic smooth muscle cells (SMCs) play a vital role in maintaining mechanical homeostasis in the aorta. We recently found that SMCs of aneurysmal aortas apply larger traction forces than SMCs of healthy aortas. This result was explained by the significant increase of hypertrophic SMCs abundance in aneurysms. In this study, we investigate whether the cytoskeleton stiffness of SMCs may also be altered in aneurysmal aortas. For that, we use atomic force microscopy (AFM) nano-indentation with a specific mode that allows subcellular-resolution mapping of the local stiffness across a specified region of interest of the cell. Aortic SMCs from a commercial human lineage (AoSMCs, Lonza) and primary aneurysmal SMCs (AnevSMCs) are cultured in conditions promoting the development of their contractile apparatus, and seeded on hydrogels with stiffness properties of 12 kPa and 25 kPa. Results show that all SMCs exhibit globally a lognormal stiffness distribution, with medians in the range 10–30 kPa. The mean of stiffness distributions is 16 kPa in aneurysmal SMCs and 12 kPa in healthy cells, but the differences are not statistically significant due to the large dispersion of AFM nano-indentation stiffness. We conclude that the possible alterations previously found in aneurysmal SMCs do not affect significantly the AFM nano-indentation stiffness of their cytoskeleton

Regulation of SMC traction forces in human aortic thoracic aneurysms

International audienc