What is the diameter of a fibrin fiber?

diameter fibrin scanning electron microscopy superresolution microscopy turbidimetry

Journal

Research and practice in thrombosis and haemostasis
ISSN: 2475-0379
Titre abrégé: Res Pract Thromb Haemost
Pays: United States
ID NLM: 101703775

Informations de publication

Date de publication:
Jul 2023
Historique:
received: 28 02 2023
revised: 31 05 2023
accepted: 05 06 2023
medline: 21 8 2023
pubmed: 21 8 2023
entrez: 21 8 2023
Statut: epublish

Résumé

Altered fibrin fiber structure is linked to pathologic states, including coronary heart disease, ischemic stroke, and atherosclerosis. However, several different techniques are commonly utilized for studying fibrin structures, and comparison of results obtained using different techniques can be challenging due to lack of standardization. This study provides a path toward standardization by comparing fibrin fiber diameters for a range of physiologic fibrinogen and thrombin concentrations using multiple different complementary experimental methods. We determined fiber diameter using scanning electron microscopy (SEM), superresolution (stochastic optical reconstruction microscopy) fluorescence microscopy, and 4 commonly utilized turbidimetric approaches to determine the congruence between the results and the conditions under which each should be used. We found that diameter values obtained using SEM and superresolution imaging agree within 10% for nearly all conditions tested. We also found that when a wavelength range of 500 to 800 nm was used for measurements and accounting for the wavelength dependence of the refractive index and specific refractive index increment, diameters obtained using the corrected Yeromonahos turbidimetric approach agree with SEM within 20% for most conditions. We performed a systematic, multitechnique survey assessing fibrin fiber diameters under a range of biochemical conditions. The similarity in the diameter values obtained using SEM and superresolution imaging suggests that drying and fixation during SEM sample preparation do not dramatically alter fiber cross-sections. Congruence, under certain conditions, between diameter values obtained using SEM, superresolution fluorescence imaging, and turbidimetry demonstrates the feasibility of a fibrin diameter standardization project.

Sections du résumé

Background UNASSIGNED
Altered fibrin fiber structure is linked to pathologic states, including coronary heart disease, ischemic stroke, and atherosclerosis. However, several different techniques are commonly utilized for studying fibrin structures, and comparison of results obtained using different techniques can be challenging due to lack of standardization.
Objectives UNASSIGNED
This study provides a path toward standardization by comparing fibrin fiber diameters for a range of physiologic fibrinogen and thrombin concentrations using multiple different complementary experimental methods.
Methods UNASSIGNED
We determined fiber diameter using scanning electron microscopy (SEM), superresolution (stochastic optical reconstruction microscopy) fluorescence microscopy, and 4 commonly utilized turbidimetric approaches to determine the congruence between the results and the conditions under which each should be used.
Results UNASSIGNED
We found that diameter values obtained using SEM and superresolution imaging agree within 10% for nearly all conditions tested. We also found that when a wavelength range of 500 to 800 nm was used for measurements and accounting for the wavelength dependence of the refractive index and specific refractive index increment, diameters obtained using the corrected Yeromonahos turbidimetric approach agree with SEM within 20% for most conditions.
Conclusion UNASSIGNED
We performed a systematic, multitechnique survey assessing fibrin fiber diameters under a range of biochemical conditions. The similarity in the diameter values obtained using SEM and superresolution imaging suggests that drying and fixation during SEM sample preparation do not dramatically alter fiber cross-sections. Congruence, under certain conditions, between diameter values obtained using SEM, superresolution fluorescence imaging, and turbidimetry demonstrates the feasibility of a fibrin diameter standardization project.

Identifiants

pubmed: 37601015
doi: 10.1016/j.rpth.2023.100285
pii: S2475-0379(23)00185-1
pmc: PMC10439396
doi:

Types de publication

Journal Article

Langues

eng

Pagination

100285

Subventions

Organisme : NHLBI NIH HHS
ID : R15 HL148842
Pays : United States

Informations de copyright

© 2023 The Author(s).

Références

Arterioscler Thromb Vasc Biol. 2011 Dec;31(12):e88-99
pubmed: 21836064
Ann Biomed Eng. 2017 May;45(5):1328-1340
pubmed: 27933406
Clin Hemorheol Microcirc. 2019 Jul 27;-1:147-153
pubmed: 31381508
Biores Open Access. 2012 Jan;1(1):34-40
pubmed: 23515363
J Thromb Haemost. 2022 Jun;20(6):1412-1420
pubmed: 35316570
Eur Heart J. 1998 Jul;19 Suppl H:H11-7
pubmed: 9717059
Adv Exp Med Biol. 1990;281:1-23
pubmed: 2129366
Neurochem Res. 2015 Nov;40(11):2220-9
pubmed: 26342829
J Thromb Haemost. 2010 Dec;8(12):2826-8
pubmed: 20961393
Thromb Haemost. 1988 Jun 16;59(3):535-9
pubmed: 3187937
Biophys J. 2013 Mar 5;104(5):1160-9
pubmed: 23473499
Biophys J. 1992 Jul;63(1):111-28
pubmed: 1420861
J Cardiovasc Risk. 1995 Jun;2(3):197-205
pubmed: 7584794
Diabetologia. 2005 Jun;48(6):1198-206
pubmed: 15864538
Biomed Res Int. 2017;2017:6385628
pubmed: 29130043
Antioxidants (Basel). 2020 Aug 12;9(8):
pubmed: 32806658
Biophys J. 1999 Nov;77(5):2813-26
pubmed: 10545379
Biophys J. 2020 Jan 7;118(1):172-181
pubmed: 31735326
Cold Spring Harb Protoc. 2013 Jun 01;2013(6):498-520
pubmed: 23734025
Acta Biomater. 2022 Mar 15;141:114-122
pubmed: 35007782
J Obstet Gynaecol Res. 2012 Apr;38(4):651-7
pubmed: 22413879
Biophys J. 2013 Jun 18;104(12):2774-5
pubmed: 23790386
Nat Methods. 2006 Oct;3(10):793-5
pubmed: 16896339
Thromb Res. 2010 Apr;125(4):357-61
pubmed: 19942259
Thromb Res. 2021 Sep;205:110-119
pubmed: 34298252
Sci Rep. 2020 May 12;10(1):7871
pubmed: 32398812
Biophys J. 2010 Oct 6;99(7):2018-27
pubmed: 20923635
Blood Coagul Fibrinolysis. 2011 Dec;22(8):696-700
pubmed: 22001525
Macromolecules. 1978 Jan-Feb;11(1):46-50
pubmed: 621951
Biomolecules. 2022 Jun 09;12(6):
pubmed: 35740932

Auteurs

Heather A Belcher (HA)

Department of Physics, East Carolina University, Greenville, NC 27858, USA.

Martin Guthold (M)

Department of Physics, Wake Forest University, Winston-Salem, NC 27109, USA.

Nathan E Hudson (NE)

Department of Physics, East Carolina University, Greenville, NC 27858, USA.

Classifications MeSH