TY - JOUR
T1 - Controlling Mesenchyme Tissue Remodeling via Spatial Arrangement of Mechanical Constraints
AU - Winston, Tackla S.
AU - Chen, Chao
AU - Suddhapas, Kantaphon
AU - Tarris, Bearett A.
AU - Elattar, Saif
AU - Sun, Shiyang
AU - Zhang, Teng
AU - Ma, Zhen
N1 - Publisher Copyright:
Copyright © 2022 Winston, Chen, Suddhapas, Tarris, Elattar, Sun, Zhang and Ma.
PY - 2022/2/18
Y1 - 2022/2/18
N2 - Tissue morphogenetic remodeling plays an important role in tissue repair and homeostasis and is often governed by mechanical stresses. In this study, we integrated an in vitro mesenchymal tissue experimental model with a volumetric contraction-based computational model to investigate how geometrical designs of tissue mechanical constraints affect the tissue remodeling processes. Both experimental data and simulation results verified that the standing posts resisted the bulk contraction of the tissues, leading to tissue thinning around the posts as gap extension and inward remodeling at the edges as tissue compaction. We changed the geometrical designs for the engineered mesenchymal tissues with different shapes of posts arrangements (triangle vs. square), different side lengths (6 mm vs. 8 mm), and insertion of a center post. Both experimental data and simulation results showed similar trends of tissue morphological changes of significant increase of gap extension and deflection compaction with larger tissues. Additionally, insertion of center post changed the mechanical stress distribution within the tissues and stabilized the tissue remodeling. This experimental-computational integrated model can be considered as a promising initiative for future mechanistic understanding of the relationship between mechanical design and tissue remodeling, which could possibly provide design rationale for tissue stability and manufacturing.
AB - Tissue morphogenetic remodeling plays an important role in tissue repair and homeostasis and is often governed by mechanical stresses. In this study, we integrated an in vitro mesenchymal tissue experimental model with a volumetric contraction-based computational model to investigate how geometrical designs of tissue mechanical constraints affect the tissue remodeling processes. Both experimental data and simulation results verified that the standing posts resisted the bulk contraction of the tissues, leading to tissue thinning around the posts as gap extension and inward remodeling at the edges as tissue compaction. We changed the geometrical designs for the engineered mesenchymal tissues with different shapes of posts arrangements (triangle vs. square), different side lengths (6 mm vs. 8 mm), and insertion of a center post. Both experimental data and simulation results showed similar trends of tissue morphological changes of significant increase of gap extension and deflection compaction with larger tissues. Additionally, insertion of center post changed the mechanical stress distribution within the tissues and stabilized the tissue remodeling. This experimental-computational integrated model can be considered as a promising initiative for future mechanistic understanding of the relationship between mechanical design and tissue remodeling, which could possibly provide design rationale for tissue stability and manufacturing.
KW - finite element analyses
KW - human induced pluripotent stem cell (hiPSC)
KW - mesenchymal stem cells
KW - tissue mechanics
KW - tissue morphogenesis
KW - tissue remodeling
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U2 - 10.3389/fbioe.2022.833595
DO - 10.3389/fbioe.2022.833595
M3 - Article
AN - SCOPUS:85125875516
SN - 2296-4185
VL - 10
JO - Frontiers in Bioengineering and Biotechnology
JF - Frontiers in Bioengineering and Biotechnology
M1 - 833595
ER -