An in silico study on the influence of extracellular matrix mechanics on vasculogenesis

dc.contributor.author
Carrasco-Mantis, A.
dc.contributor.author
Alarcón, T.
dc.contributor.author
Sanz-Herrera, J.A.
dc.date.accessioned
2023-06-21T13:11:07Z
dc.date.accessioned
2024-09-19T14:25:25Z
dc.date.available
2023-06-21T13:11:07Z
dc.date.available
2024-09-19T14:25:25Z
dc.date.issued
2023-04-01
dc.identifier.uri
http://hdl.handle.net/2072/535456
dc.description.abstract
Background and objectives: Blood vessels form a network of capillaries throughout the body that perform essential functions for life. Vasculogenesis, i.e. the formation of new blood vessels, is regulated by many factors, biochemical ones being among the most important. However, others such as the biomechanical influence on shape, organization and structure of vessel networks require further investigation. In this paper, we develop a 3D agent-based mechanobiological model of vasculogenesis with the aim of analyzing how the mechanics of the extracellular matrix (ECM) affects vasculogenesis. Methods: For this purpose, we consider a growing domain composed of different cells: tip cells, which are the driving cells located at the end of the vessels and stalk cells, which are found in the interior of the vascular network. ECM is considered as particles (agents) that surround the growth of the vascular network. Depending on the cell type, different sets of forces are considered, such as chemotactic, mechanical, random and viscoelastic forces among others. Results: The growth of the network is iteratively analyzed and updated at each time step based on a mechanically-driven proliferation rule. The influence of different biomechanical factors, such as ECM stiffness or viscoelasticity are explored through in silico simulations. A number of indicators are defined along the algorithm, like number of cells, branches, tortuosity and anisotropy, in order to compare topological differences of the vascular network during vasculogenesis under different ECM conditions. The obtained results are qualitatively compared with other related works in the literature. Conclusions: The present study sheds some light and partially explain, from an in silico perspective, the role of ECM mechanics on vasculogenesis. The main conclusions of this work are: (i) increased stiffness increases proliferation, (ii) the network tends to migrate towards stiffer areas, and (iii) increased viscoelasticity decreases proliferation. © 2023 The Author(s)
eng
dc.description.sponsorship
The authors gratefully acknowledge the financial support from projects PGC2018-097257-B-C31 and PID2021-126051OB-C42 by the Ministerio de Ciencia e Innovación (MCI), Agencia Estatal de Investigación (AEI) and Fondo Europeo de Desarrollo Regional (FEDER), and project P20-01195 funded by the Consejerá de Economá, Conocimiento, Empresas y Universidad de la Junta de Andalucá. A.C.-M. was supported by grant PRE2019-090391. This work also acknowledges the CERCA Programme of the Generalitat de Catalunya for institutional support. This work was also supported by the Spanish State Research Agency, through the Severo Ochoa and Maria de Maeztu Program for Centres and Units of Excellence in R&D (CEX2020-001084-M).
dc.format.extent
12 p.
dc.language.iso
eng
dc.publisher
Elsevier Ireland Ltd
dc.relation.ispartof
Computer Methods and Programs in Biomedicine
dc.rights
L'accés als continguts d'aquest document queda condicionat a l'acceptació de les condicions d'ús establertes per la següent llicència Creative Commons: http://creativecommons.org/licenses/by-nc-nd/4.0/
dc.source
RECERCAT (Dipòsit de la Recerca de Catalunya)
dc.subject.other
Agent-based model; Cellular mechanics; Extracellular matrix; Mechanobiology; Vasculogenesis; Viscoelasticity
dc.title
An in silico study on the influence of extracellular matrix mechanics on vasculogenesis
dc.type
info:eu-repo/semantics/article
dc.type
info:eu-repo/semantics/publishedVersion
dc.embargo.terms
cap
dc.identifier.doi
10.1016/j.cmpb.2023.107369
dc.rights.accessLevel
info:eu-repo/semantics/openAccess


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