Using interconnected viscoelastic elements to investigate forces and the role of cell properties during cell migration.
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| Title: | Using interconnected viscoelastic elements to investigate forces and the role of cell properties during cell migration. |
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| Authors: | Xu, Yuehui1 (AUTHOR), Zhu, Luoding1 (AUTHOR), Opafola, Faith2 (AUTHOR), Liu, Jing3 (AUTHOR), Barber, Jared1 (AUTHOR) jarobarb@iu.edu |
| Source: | Mathematical Biosciences. Jun2026, Vol. 396, pN.PAG-N.PAG. 1p. |
| Subjects: | Cell migration, Focal adhesions, Mathematical models, Cellular mechanics, Viscoelastic materials, Sensitivity analysis, Simulation methods & models |
| Abstract: | • Interconnected viscoelastic elements model a 3D migrating cell. • Focal adhesions arise in a lamellipodia-like protrusion and connect with a substrate. • A mathematical and computational model of cell migration is experimentally validated. • A sensitivity analysis of elastic and other factors affecting cell migration is done. We build a model of a general three-dimensional cell migrating across a flat substrate using an interconnected network of viscoelastic elements (damped springs). While the end goal is to use the model to investigate forces in migrating biological cells, the goal here is to demonstrate the model's validity, practical feasibility, and capability. We first show qualitative agreement with experiment including reasonable shape and speed, higher protrusive forces correlating with higher focal adhesion forces, and higher adhesive forces near the cell's front and back. We then show the model can produce estimates of deformation and stresses in migrating cells. We lastly perform a sensitivity analysis demonstrating that 1) cell length is increased by increasing driving force and focal adhesion attachment strength and by decreasing reference volume, 2) cell speed is increased by decreasing cell membrane-substrate interaction and increasing driving force, and 3) focal adhesion forces are increased by decreasing membrane elasticity and number of focal adhesions. Our results suggest that future model calibration will yield useful insights into how cell forces affect migration. [ABSTRACT FROM AUTHOR] |
| Copyright of Mathematical Biosciences is the property of Elsevier B.V. and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.) | |
| Database: | Engineering Source |
| FullText | Text: Availability: 0 |
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| Header | DbId: egs DbLabel: Engineering Source An: 193288439 AccessLevel: 6 PubType: Periodical PubTypeId: serialPeriodical PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Using interconnected viscoelastic elements to investigate forces and the role of cell properties during cell migration. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AR" term="%22Xu%2C+Yuehui%22">Xu, Yuehui</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Zhu%2C+Luoding%22">Zhu, Luoding</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Opafola%2C+Faith%22">Opafola, Faith</searchLink><relatesTo>2</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Liu%2C+Jing%22">Liu, Jing</searchLink><relatesTo>3</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Barber%2C+Jared%22">Barber, Jared</searchLink><relatesTo>1</relatesTo> (AUTHOR)<i> jarobarb@iu.edu</i> – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22Mathematical+Biosciences%22">Mathematical Biosciences</searchLink>. Jun2026, Vol. 396, pN.PAG-N.PAG. 1p. – Name: Subject Label: Subjects Group: Su Data: <searchLink fieldCode="DE" term="%22Cell+migration%22">Cell migration</searchLink><br /><searchLink fieldCode="DE" term="%22Focal+adhesions%22">Focal adhesions</searchLink><br /><searchLink fieldCode="DE" term="%22Mathematical+models%22">Mathematical models</searchLink><br /><searchLink fieldCode="DE" term="%22Cellular+mechanics%22">Cellular mechanics</searchLink><br /><searchLink fieldCode="DE" term="%22Viscoelastic+materials%22">Viscoelastic materials</searchLink><br /><searchLink fieldCode="DE" term="%22Sensitivity+analysis%22">Sensitivity analysis</searchLink><br /><searchLink fieldCode="DE" term="%22Simulation+methods+%26+models%22">Simulation methods & models</searchLink> – Name: Abstract Label: Abstract Group: Ab Data: • Interconnected viscoelastic elements model a 3D migrating cell. • Focal adhesions arise in a lamellipodia-like protrusion and connect with a substrate. • A mathematical and computational model of cell migration is experimentally validated. • A sensitivity analysis of elastic and other factors affecting cell migration is done. We build a model of a general three-dimensional cell migrating across a flat substrate using an interconnected network of viscoelastic elements (damped springs). While the end goal is to use the model to investigate forces in migrating biological cells, the goal here is to demonstrate the model's validity, practical feasibility, and capability. We first show qualitative agreement with experiment including reasonable shape and speed, higher protrusive forces correlating with higher focal adhesion forces, and higher adhesive forces near the cell's front and back. We then show the model can produce estimates of deformation and stresses in migrating cells. We lastly perform a sensitivity analysis demonstrating that 1) cell length is increased by increasing driving force and focal adhesion attachment strength and by decreasing reference volume, 2) cell speed is increased by decreasing cell membrane-substrate interaction and increasing driving force, and 3) focal adhesion forces are increased by decreasing membrane elasticity and number of focal adhesions. Our results suggest that future model calibration will yield useful insights into how cell forces affect migration. [ABSTRACT FROM AUTHOR] – Name: AbstractSuppliedCopyright Label: Group: Ab Data: <i>Copyright of Mathematical Biosciences is the property of Elsevier B.V. and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract.</i> (Copyright applies to all Abstracts.) |
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| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1016/j.mbs.2026.109682 Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 1 StartPage: N.PAG Subjects: – SubjectFull: Cell migration Type: general – SubjectFull: Focal adhesions Type: general – SubjectFull: Mathematical models Type: general – SubjectFull: Cellular mechanics Type: general – SubjectFull: Viscoelastic materials Type: general – SubjectFull: Sensitivity analysis Type: general – SubjectFull: Simulation methods & models Type: general Titles: – TitleFull: Using interconnected viscoelastic elements to investigate forces and the role of cell properties during cell migration. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Xu, Yuehui – PersonEntity: Name: NameFull: Zhu, Luoding – PersonEntity: Name: NameFull: Opafola, Faith – PersonEntity: Name: NameFull: Liu, Jing – PersonEntity: Name: NameFull: Barber, Jared IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 06 Text: Jun2026 Type: published Y: 2026 Identifiers: – Type: issn-print Value: 00255564 Numbering: – Type: volume Value: 396 Titles: – TitleFull: Mathematical Biosciences Type: main |
| ResultId | 1 |