A Fibrocontractive Mechanochemical Model of Dermal Wound Closure Incorporating Realistic Growth Factor Kinetics

Kelly E. Murphy; Cameron L. Hall; Philip K. Maini; Scott W. McCue; D. L. Sean McElwain

doi:10.1007/s11538-011-9712-y

A Fibrocontractive Mechanochemical Model of Dermal Wound Closure Incorporating Realistic Growth Factor Kinetics

Kelly E. Murphy, Cameron L. Hall, Philip K. Maini, Scott W. McCue, D. L. Sean McElwain

Research output: Contribution to journal › Article › peer-review

36 Scopus citations

Abstract

Fibroblasts and their activated phenotype, myofibroblasts, are the primary cell types involved in the contraction associated with dermal wound healing. Recent experimental evidence indicates that the transformation from fibroblasts to myofibroblasts involves two distinct processes: The cells are stimulated to change phenotype by the combined actions of transforming growth factor β (TGFβ) and mechanical tension. This observation indicates a need for a detailed exploration of the effect of the strong interactions between the mechanical changes and growth factors in dermal wound healing. We review the experimental findings in detail and develop a model of dermal wound healing that incorporates these phenomena. Our model includes the interactions between TGFβ and collagenase, providing a more biologically realistic form for the growth factor kinetics than those included in previous mechanochemical descriptions. A comparison is made between the model predictions and experimental data on human dermal wound healing and all the essential features are well matched. © 2012 Society for Mathematical Biology.

Original language	English (US)
Pages (from-to)	1143-1170
Number of pages	28
Journal	Bulletin of Mathematical Biology
Volume	74
Issue number	5
DOIs	https://doi.org/10.1007/s11538-011-9712-y
State	Published - Jan 13 2012
Externally published	Yes

Bibliographical note

KAUST Repository Item: Exported on 2020-10-01
Acknowledged KAUST grant number(s): KUK-C1-013-04
Acknowledgements: This research is primarily supported under the Australian Research Council's Discovery Projects funding scheme (project number DP0878011), the Institute of Health and Biomedical Innovation at Queensland University of Technology, and by the Centre for Mathematical Biology, Mathematical Institute at the University of Oxford. PKM was partially supported by a Queensland University of Technology Adjunct Professorship and a Royal Society Wolfson Research Merit Award. This publication was based on work supported in part by Award No. KUK-C1-013-04, made by King Abdullah University of Science and Technology (KAUST).
This publication acknowledges KAUST support, but has no KAUST affiliated authors.

Access to Document

10.1007/s11538-011-9712-y

Cite this

@article{57560c7141db4671b005eb1c7739e5b5,

title = "A Fibrocontractive Mechanochemical Model of Dermal Wound Closure Incorporating Realistic Growth Factor Kinetics",

abstract = "Fibroblasts and their activated phenotype, myofibroblasts, are the primary cell types involved in the contraction associated with dermal wound healing. Recent experimental evidence indicates that the transformation from fibroblasts to myofibroblasts involves two distinct processes: The cells are stimulated to change phenotype by the combined actions of transforming growth factor β (TGFβ) and mechanical tension. This observation indicates a need for a detailed exploration of the effect of the strong interactions between the mechanical changes and growth factors in dermal wound healing. We review the experimental findings in detail and develop a model of dermal wound healing that incorporates these phenomena. Our model includes the interactions between TGFβ and collagenase, providing a more biologically realistic form for the growth factor kinetics than those included in previous mechanochemical descriptions. A comparison is made between the model predictions and experimental data on human dermal wound healing and all the essential features are well matched. {\textcopyright} 2012 Society for Mathematical Biology.",

author = "Murphy, {Kelly E.} and Hall, {Cameron L.} and Maini, {Philip K.} and McCue, {Scott W.} and McElwain, {D. L. Sean}",

note = "KAUST Repository Item: Exported on 2020-10-01 Acknowledged KAUST grant number(s): KUK-C1-013-04 Acknowledgements: This research is primarily supported under the Australian Research Council's Discovery Projects funding scheme (project number DP0878011), the Institute of Health and Biomedical Innovation at Queensland University of Technology, and by the Centre for Mathematical Biology, Mathematical Institute at the University of Oxford. PKM was partially supported by a Queensland University of Technology Adjunct Professorship and a Royal Society Wolfson Research Merit Award. This publication was based on work supported in part by Award No. KUK-C1-013-04, made by King Abdullah University of Science and Technology (KAUST). This publication acknowledges KAUST support, but has no KAUST affiliated authors.",

year = "2012",

month = jan,

day = "13",

doi = "10.1007/s11538-011-9712-y",

language = "English (US)",

volume = "74",

pages = "1143--1170",

journal = "Bulletin of Mathematical Biology",

issn = "0092-8240",

publisher = "Springer New York",

number = "5",

}

TY - JOUR

T1 - A Fibrocontractive Mechanochemical Model of Dermal Wound Closure Incorporating Realistic Growth Factor Kinetics

AU - Murphy, Kelly E.

AU - Hall, Cameron L.

AU - Maini, Philip K.

AU - McCue, Scott W.

AU - McElwain, D. L. Sean

N1 - KAUST Repository Item: Exported on 2020-10-01 Acknowledged KAUST grant number(s): KUK-C1-013-04 Acknowledgements: This research is primarily supported under the Australian Research Council's Discovery Projects funding scheme (project number DP0878011), the Institute of Health and Biomedical Innovation at Queensland University of Technology, and by the Centre for Mathematical Biology, Mathematical Institute at the University of Oxford. PKM was partially supported by a Queensland University of Technology Adjunct Professorship and a Royal Society Wolfson Research Merit Award. This publication was based on work supported in part by Award No. KUK-C1-013-04, made by King Abdullah University of Science and Technology (KAUST). This publication acknowledges KAUST support, but has no KAUST affiliated authors.

PY - 2012/1/13

Y1 - 2012/1/13

N2 - Fibroblasts and their activated phenotype, myofibroblasts, are the primary cell types involved in the contraction associated with dermal wound healing. Recent experimental evidence indicates that the transformation from fibroblasts to myofibroblasts involves two distinct processes: The cells are stimulated to change phenotype by the combined actions of transforming growth factor β (TGFβ) and mechanical tension. This observation indicates a need for a detailed exploration of the effect of the strong interactions between the mechanical changes and growth factors in dermal wound healing. We review the experimental findings in detail and develop a model of dermal wound healing that incorporates these phenomena. Our model includes the interactions between TGFβ and collagenase, providing a more biologically realistic form for the growth factor kinetics than those included in previous mechanochemical descriptions. A comparison is made between the model predictions and experimental data on human dermal wound healing and all the essential features are well matched. © 2012 Society for Mathematical Biology.

AB - Fibroblasts and their activated phenotype, myofibroblasts, are the primary cell types involved in the contraction associated with dermal wound healing. Recent experimental evidence indicates that the transformation from fibroblasts to myofibroblasts involves two distinct processes: The cells are stimulated to change phenotype by the combined actions of transforming growth factor β (TGFβ) and mechanical tension. This observation indicates a need for a detailed exploration of the effect of the strong interactions between the mechanical changes and growth factors in dermal wound healing. We review the experimental findings in detail and develop a model of dermal wound healing that incorporates these phenomena. Our model includes the interactions between TGFβ and collagenase, providing a more biologically realistic form for the growth factor kinetics than those included in previous mechanochemical descriptions. A comparison is made between the model predictions and experimental data on human dermal wound healing and all the essential features are well matched. © 2012 Society for Mathematical Biology.

UR - http://hdl.handle.net/10754/597267

UR - http://link.springer.com/10.1007/s11538-011-9712-y

UR - http://www.scopus.com/inward/record.url?scp=84859213144&partnerID=8YFLogxK

U2 - 10.1007/s11538-011-9712-y

DO - 10.1007/s11538-011-9712-y

M3 - Article

C2 - 22246694

SN - 0092-8240

VL - 74

SP - 1143

EP - 1170

JO - Bulletin of Mathematical Biology

JF - Bulletin of Mathematical Biology

IS - 5

ER -

A Fibrocontractive Mechanochemical Model of Dermal Wound Closure Incorporating Realistic Growth Factor Kinetics

Abstract

Bibliographical note

Access to Document

Other files and links

Fingerprint

Cite this