Strength and deformability of fibrin clots: Biomechanics, thermodynamics, and mechanisms of rupture.

Cracked fibrin gel Fluctuating Spring model Rupture of fibrin clots Stress-strain spectra Thermodynamics of rupture

Journal

Acta biomaterialia
ISSN: 1878-7568
Titre abrégé: Acta Biomater
Pays: England
ID NLM: 101233144

Informations de publication

Date de publication:
01 09 2021
Historique:
received: 15 03 2021
revised: 28 06 2021
accepted: 29 06 2021
pubmed: 8 7 2021
medline: 1 9 2021
entrez: 7 7 2021
Statut: ppublish

Résumé

Fibrin is the major determinant of the mechanical stability and integrity of blood clots and thrombi. To explore the rupture of blood clots, emulating thrombus breakage, we stretched fibrin gels with single-edge cracks of varying size. Ultrastructural alterations of the fibrin network correlated with three regimes of stress vs. strain profiles: the weakly non-linear regime due to alignment of fibrin fibers; linear regime owing to further alignment and stretching of fibers; and the rupture regime for large deformations reaching the critical strain and stress, at which irreversible breakage of fibers ahead of the crack tip occurs. To interpret the stress-strain curves, we developed a new Fluctuating Spring model, which maps the fibrin alignment at the characteristic strain, network stretching with the Young modulus, and simultaneous cooperative rupture of coupled fibrin fibers into a theoretical framework to obtain the closed-form expressions for the strain-dependent stress profiles. Cracks render network rupture stochastic, and the free energy change for fiber deformation and rupture decreases with the crack length, making network rupture more spontaneous. By contrast, mechanical cooperativity due to the presence of inter-fiber contacts strengthens fibrin networks. The results obtained provide a fundamental understanding of blood clot breakage that underlies thrombotic embolization. STATEMENT OF SIGNIFICANCE: Fibrin, a naturally occurring biomaterial, is the major determinant of mechanical stability and integrity of blood clots and obstructive thrombi. We tested mechanically fibrin gels with single-edge cracks and followed ultrastructural alterations of the fibrin network. Rupture of fibrin gel involves initial alignment and elastic stretching of fibers followed by their eventual rupture for deformations reaching the critical level. To interpret the stress-strain curves, we developed Fluctuating Spring model, which showed that cracks render rupture of fibrin networks more spontaneous; yet, coupled fibrin fibers reinforce cracked fibrin networks. The results obtained provide fundamental understanding of blood clot breakage that underlies thrombotic embolization. Fluctuating Spring model can be applied to other protein networks with cracks and to interpret the stress-strain profiles.

Identifiants

pubmed: 34233219
pii: S1742-7061(21)00428-1
doi: 10.1016/j.actbio.2021.06.046
pmc: PMC8483248
mid: NIHMS1723400
pii:
doi:

Substances chimiques

Fibrin 9001-31-4

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

355-369

Subventions

Organisme : NHLBI NIH HHS
ID : R01 HL135254
Pays : United States
Organisme : NHLBI NIH HHS
ID : R00 HL148646
Pays : United States
Organisme : NHLBI NIH HHS
ID : K99 HL148646
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL148227
Pays : United States
Organisme : NIH HHS
ID : S10 OD018041
Pays : United States

Informations de copyright

Copyright © 2021 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

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Auteurs

Valerie Tutwiler (V)

Department of Cell and Developmental Biology, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA 19104, USA.

Farkhad Maksudov (F)

Department of Chemistry, University of Massachusetts, Lowell, MA 01854, USA.

Rustem I Litvinov (RI)

Department of Cell and Developmental Biology, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA 19104, USA; Institute of Fundamental Medicine and Biology, Kazan Federal University, Kazan 420008, Russian Federation.

John W Weisel (JW)

Department of Cell and Developmental Biology, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA 19104, USA. Electronic address: weisel@pennmedicine.upenn.edu.

Valeri Barsegov (V)

Department of Chemistry, University of Massachusetts, Lowell, MA 01854, USA. Electronic address: Valeri_Barsegov@uml.edu.

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Classifications MeSH