scholarly journals A Phenomenological Model for Mechanically Mediated Growth, Remodeling, Damage, and Plasticity of Gel-Derived Tissue Engineered Blood Vessels

2009 ◽  
Vol 131 (10) ◽  
Author(s):  
Julia Raykin ◽  
Alexander I. Rachev ◽  
Rudolph L. Gleason

Mechanical stimulation has been shown to dramatically improve mechanical and functional properties of gel-derived tissue engineered blood vessels (TEBVs). Adjusting factors such as cell source, type of extracellular matrix, cross-linking, magnitude, frequency, and time course of mechanical stimuli (among many other factors) make interpretation of experimental results challenging. Interpretation of data from such multifactor experiments requires modeling. We present a modeling framework and simulations for mechanically mediated growth, remodeling, plasticity, and damage of gel-derived TEBVs that merge ideas from classical plasticity, volumetric growth, and continuum damage mechanics. Our results are compared with published data and suggest that this model framework can predict the evolution of geometry and material behavior under common experimental loading scenarios.

2008 ◽  
Vol 57 ◽  
pp. 226-234 ◽  
Author(s):  
Rudolph L. Gleason ◽  
William Wan

There is a great unmet clinical need to develop small diameter tissue engineered blood vessels (TEBV) with low thrombogenicity and immune response and suitable mechanical properties. In this paper we describe experimental and computational frameworks to characterize the use of mechanical stimuli to improve the mechanical properties of TEBVs. We model the TEBV as a constrained mixture and track the production, degradation, mechanical state, and organization of each structural constituent. Specifically, we assume that individual load bearing constituents can co-exist within each neighborhood and, although they are constrained to deform together, each constituent within this neighborhood may have different natural (i.e., stress-free) configurations. Motivated by this theoretical framework, we have designed a bioreactor and biomechanical testing device for TEBVs. This device is designed to provide precise and independent control of mean and cyclic luminal flow rate, transmural pressure, and axial load over weeks and months in culture and perform intermittent biaxial biomechanical tests. This device also fits under a two-photon laser scanning microscope for 3-dimenstional imaging of the content and organization of cells and matrix constituents. These data directly support our theoretical model.


2008 ◽  
Vol 75 (3) ◽  
Author(s):  
Jayesh R. Jain ◽  
Somnath Ghosh

This paper develops a microscopic homogenization based continuum damage mechanics (HCDM) model framework for fiber reinforced composites undergoing interfacial debonding. It is an advancement over the 2D HCDM model developed by Raghavan and Ghosh (2005, “A Continuum Damage Mechanics Model for Unidirectional Composites Undergoing Interfacial Debonding,” Mech. Mater., 37(9), pp. 955–979), which does not yield accurate results for nonproportional loading histories. The present paper overcomes this shortcoming through the introduction of a principal damage coordinate system (PDCS) in the HCDM representation, which evolves with loading history. The material behavior is represented as a continuum constitutive law involving a fourth order orthotropic tensor with stiffness characterized as a macroscopic internal variable. The current work also extends the model of Raghavan and Ghosh to incorporate damage in 3D composites through functional forms of the fourth order damage tensor in terms of macroscopic strain components. The model is calibrated by homogenizing the micromechanical response of the representative volume element (RVE) for a few strain histories. This parametric representation can significantly enhance the computational efficiency of the model by avoiding the cumbersome strain space interpolations. The proposed model is validated by comparing the CDM results with homogenized micromechanical response of single and multiple fiber RVEs subjected to arbitrary loading history.


2020 ◽  
Vol 134 (17) ◽  
pp. 2399-2418
Author(s):  
Yoshito Yamashiro ◽  
Hiromi Yanagisawa

Abstract Blood vessels are constantly exposed to mechanical stimuli such as shear stress due to flow and pulsatile stretch. The extracellular matrix maintains the structural integrity of the vessel wall and coordinates with a dynamic mechanical environment to provide cues to initiate intracellular signaling pathway(s), thereby changing cellular behaviors and functions. However, the precise role of matrix–cell interactions involved in mechanotransduction during vascular homeostasis and disease development remains to be fully determined. In this review, we introduce hemodynamics forces in blood vessels and the initial sensors of mechanical stimuli, including cell–cell junctional molecules, G-protein-coupled receptors (GPCRs), multiple ion channels, and a variety of small GTPases. We then highlight the molecular mechanotransduction events in the vessel wall triggered by laminar shear stress (LSS) and disturbed shear stress (DSS) on vascular endothelial cells (ECs), and cyclic stretch in ECs and vascular smooth muscle cells (SMCs)—both of which activate several key transcription factors. Finally, we provide a recent overview of matrix–cell interactions and mechanotransduction centered on fibronectin in ECs and thrombospondin-1 in SMCs. The results of this review suggest that abnormal mechanical cues or altered responses to mechanical stimuli in EC and SMCs serve as the molecular basis of vascular diseases such as atherosclerosis, hypertension and aortic aneurysms. Collecting evidence and advancing knowledge on the mechanotransduction in the vessel wall can lead to a new direction of therapeutic interventions for vascular diseases.


Author(s):  
Benjamin Wassermann ◽  
Nina Korshunova ◽  
Stefan Kollmannsberger ◽  
Ernst Rank ◽  
Gershon Elber

AbstractThis paper proposes an extension of the finite cell method (FCM) to V-rep models, a novel geometric framework for volumetric representations. This combination of an embedded domain approach (FCM) and a new modeling framework (V-rep) forms the basis for an efficient and accurate simulation of mechanical artifacts, which are not only characterized by complex shapes but also by their non-standard interior structure. These types of objects gain more and more interest in the context of the new design opportunities opened by additive manufacturing, in particular when graded or micro-structured material is applied. Two different types of functionally graded materials (FGM) are considered: The first one, multi-material FGM is described using the inherent property of V-rep models to assign different properties throughout the interior of a domain. The second, single-material FGM—which is heterogeneously micro-structured—characterizes the effective material behavior of representative volume elements by homogenization and performs large-scale simulations using the embedded domain approach.


2021 ◽  
pp. 1-13
Author(s):  
Kaveh Sanaei ◽  
Sydney Plotner ◽  
Anson Oommen Jacob ◽  
Jaime Ramirez-Vick ◽  
Narendra Vyavahare ◽  
...  

BACKGROUND: The main objective of tissue engineering is to fabricate a tissue construct that mimics native tissue both biologically and mechanically. A recurring problem for tissue-engineered blood vessels (TEBV) is deficient elastogenesis from seeded smooth muscle cells. Elastin is an integral mechanical component in blood vessels, allowing elastic deformation and retraction in response to the shear and pulsatile forces of the cardiac system. OBJECTIVE: The goal of this research is to assess the effect of the vitamin A derivative all-trans retinoic acid (RA) and polyphenol pentagalloyl glucose (PGG) on the expression of elastin in human aortic smooth muscle cells (hASMC). METHODS: A polycaprolactone (PCL) and the gelatin polymer composite was electrospun and doped with RA and PGG. The scaffolds were subsequently seeded with hASMCs and incubated for five weeks. The resulting tissue-engineered constructs were evaluated using qPCR and Fastin assay for their elastin expression and deposition. RESULTS: All treatments showed an increased elastin expression compared to the control, with PGG treatments showing a significant increase in gene expression and elastin deposition.


2006 ◽  
Vol 12 (4) ◽  
pp. 831-842 ◽  
Author(s):  
Sepideh Heydarkhan-Hagvall ◽  
Maricris Esguerra ◽  
Gisela Helenius ◽  
Rigmor Söderberg ◽  
Bengt R. Johansson ◽  
...  

2021 ◽  
pp. 2000428
Author(s):  
Jounghyun H. Lee ◽  
Zaozao Chen ◽  
Siyu He ◽  
JoyceK. Zhou ◽  
Alexander Tsai ◽  
...  

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