Cited by 457Electrospun Nanofibers in Biomedical ApplicationsBone Tissue Engineering MaterialsTissue Engineering and Regenerative Medicine

The DOI matches its Crossref record; 43 of the 43 references it cites were found in a registry or an index; none of the 23 sources its claims cite is checked for support yet.

Macrophage functional polarization (M1/M2) in response to varying fiber and pore dimensions of electrospun scaffolds

Open access
Garg, Koyal, Pullen, Nicholas A., Oskeritzian, Carole A., Ryan, John J., Bowlin, Gary L.·2013·Biomaterials

Abstract

In this study, we investigated the effect of fiber and pore size of an electrospun scaffold on the polarization of mouse bone marrow-derived macrophages (BMMΦs) towards regenerative (M2) or inflammatory (M1) phenotypes. BMMΦs were seeded on Polydioxanone (PDO) scaffolds electrospun from varying polymer concentrations (60, 100, and 140 mg/ml). Higher polymer concentrations yielded larger diameter fibers with larger pore sizes and porosity. BMMΦ cultured on these scaffolds showed a correlation between increasing fiber/pore size and increased expression of the M2 marker Arginase 1 (Arg1), along with decreased expression of the M1 marker inducible nitric oxide synthase (iNOS). Secretion of the angiogenic cytokines VEGF, TGF-β1 and bFGF was higher among cultures employing larger fiber/pore size scaffolds (140 mg/ml). Using a 3D in vitro angiogenesis bead assay, we have demonstrated that the M2-like profile of BMMΦ induced by the 140 mg/ml is functional. Furthermore, our results show that the pore size of a scaffold is a more critical regulator of the BMMΦ polarization compared to the fiber diameter. The study also shows a potential role for MyD88 in regulating M1 BMMΦ signaling on the large vs. small fiber/pore size PDO scaffold. These data are instructive for the rationale design of implantable prosthetics designed to promote in situ regeneration.

Overview

Integrity signals

Registry

Crossref · 10.1016/j.biomaterials.2013.02.065

Cites

43 of 43 references verified0 citation errors · 0 not checkable

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Claims the paper makes

53 Own result · 17 Own interpretation · 16 Not checked yet · 3 No basis given · 2 Own method

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  • It may state two separate claims as one. 22
  • Probably not a substantial claim. 12
32 of 32
  • The paper relies on this without support.

    In vitro BMMΦ responses to PDO scaffolds predict in vivo regeneration.

    “These data are instructive for the rationale design of implantable prosthetics designed to promote in situ regeneration.”
  • The paper relies on this without support.

    The differences in BMMΦ response across PDO scaffolds are due to fiber/pore size rather than other scaffold properties.

    “BMMΦ cultured on these scaffolds showed a correlation between increasing fiber/pore size and increased expression of the M2 marker Arginase 1 (Arg1), along with decreased expression of the M1 marker inducible nitric oxide synthase (iNOS).”
  • The paper relies on this without support.

    An M2 macrophage phenotype promotes healing and integration of the biomaterial with the host tissue, enhancing tissue regeneration.

    “Such a functional M2 phenotype is likely to promote healing and integration of the biomaterial with the host tissue to enhance tissue regeneration.”
  • The paper relies on this without support.

    In vitro macrophage responses to scaffold architecture predict in vivo tissue regeneration outcomes.

    “These data are instructive for the design and engineering of biomaterials that can promote in situ angiogenesis and tissue regeneration.”
4 of 4

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2 of 2

Citations

Cites

Research works printed but not linked: 1

  1. General chapter <85> bacterial endotoxins test, US pharmacopeia 31-national formulary 26. United States Pharmacopeial Convention, Rockville, MD; 2009.

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Metadata

Authors
Garg, K., Pullen, N. A., Oskeritzian, C. A., Ryan, J. J., & Bowlin, G. L.
Affiliations
Virginia Commonwealth University (US)
Corresponding author
Bowlin, Gary L.
Venue
Biomaterials
Publisher
Elsevier BV
Published
2013-06
Volume
34
Issue
18
Pages
4439-4451
ISSN
0142-9612 (ISSN-L)
OpenAlex
W2070438219
Cited by
457
References
43
Citations by year
2026: 28 · 2025: 35 · 2024: 40 · 2023: 35 · 2022: 48 · 2021: 65 · 2020: 55 · 2019: 39 · 2018: 24 · 2017: 26 · 2016: 32 · 2015: 12 · 2014: 17 · 2013: 1
FWCI
7.34
Type
journal article
Language
en
Open access
Locations
  • Biomaterials (publishedVersion)
  • PubMed (publishedVersion)
  • Europe PMC (PubMed Central) (acceptedVersion)
  • PubMed Central (acceptedVersion)
Funders
  • National Institute of General Medical Sciences (K12GM093857)
  • National Institute of Allergy and Infectious Diseases (R01AI059638, R01AI095494)
Topics
  • Physical Sciences › Materials Science › Biomaterials › Electrospun Nanofibers in Biomedical Applications
  • Physical Sciences › Engineering › Biomedical Engineering › Bone Tissue Engineering Materials
  • Health Sciences › Medicine › Surgery › Tissue Engineering and Regenerative Medicine
Keywords
macrophage polarization, M1/M2 macrophages, electrospun scaffolds, fiber diameter, pore size, polydioxanone, bone marrow-derived macrophages, arginase-1, inducible nitric oxide synthase, angiogenic cytokines, vascular endothelial growth factor, TGF-β1, basic fibroblast growth factor, MyD88, scaffold porosity, tissue regeneration
MeSH terms
Animals, Arginase, Bone Marrow Cells, Endotoxins, Macrophages, Mice, Inbred C57BL, Microscopy, Electron, Scanning, Phenotype, Signal Transduction, Porosity, Polydioxanone, Cell Polarity, Culture Media, Conditioned, Neovascularization, Physiologic, Tissue Engineering, Endothelial Cells, Mice, Nitric Oxide Synthase Type II, Myeloid Differentiation Factor 88, Tissue Scaffolds

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