Cited by 25Cellular Mechanics and InteractionsInterstitial Lung Diseases and Idiopathic Pulmonary FibrosisTissue Engineering and Regenerative Medicine

Collagen morphology influences macrophage shape and marker expression in?vitro

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Vasse, Gwenda F., Kühn, Philipp T., Zhou, Qihui, Bhusari, Shardul A., Reker-Smit, Catharina, Melgert, Barbro N., van Rijn, Patrick·2018·Journal of Immunology and Regenerative Medicine

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Registry

Crossref · 10.1016/j.regen.2018.01.002

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39 of 39 references verified0 citation errors · 0 not checkable

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  • M1 macrophages have an egg-shaped morphology, while M2 macrophages exhibit a more spindle-shaped morphology.

    “It has been proved that M1 macrophages have an egg-shaped morphology, while M2 macrophages exhibited a more spindle-shaped morphology [31,38].”

    From Substrate stiffness modulates bone marrow-derived macrophage polarization through NF-κB signaling pathway (2020) · cites this paper as [31]

    In the Discussion passage headed “Combining these” (page not provided), the paper reports that collagen changed macrophage shape without changing macrophage subsets. It says a particular phenotype does not necessarily restrict macrophages to a certain shape, rather than establishing egg-shaped M1 and spindle-shaped M2 morphologies. (LLM, conf=0.86)

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  • CD68 and CD86 are markers for M1 macrophages, and CD68 and CD206 are markers for M2 macrophages.

    “Macrophage phenotypic markers, CD68 and CD86 for M1 and CD68 and CD206 for M2, were selected following the previous study [31,32].”

    From Substrate stiffness modulates bone marrow-derived macrophage polarization through NF-κB signaling pathway (2020) · cites this paper as [31]

    Section 2.5 defines M2 macrophages as CD206-high, supporting CD206 as an M2 marker. It defines M1 using MHCII-high and CD206-low, and does not identify CD68 or CD86 as markers for either phenotype. No page number is available in our copy. (LLM, conf=0.88)

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Research works printed but not linked: 1

  1. [21]21. Blakney AK, Swartzlander MD, Bryant SJ. The effects of substrate stiffness on the in vitro activation of macrophages and in vivo host response to poly(- ethylene glycol)-based hydrogels. J Biomed Mater Res A. 2012;100:1375e1386.

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Authors
Vasse, G. F., Kühn, P. T., Zhou, Q., Bhusari, S. A., Reker-Smit, C., Melgert, B. N., & van Rijn, P.
Affiliations
University Medical Center Groningen (NL)
Corresponding author
Melgert, Barbro N.
Venue
Journal of Immunology and Regenerative Medicine
Publisher
Elsevier BV
Published
2018-03
Volume
1
Pages
13-20
ISSN
2468-4988 (ISSN-L)
OpenAlex
W2802861923
Cited by
25
References
39
Citations by year
2026: 2 · 2025: 4 · 2024: 3 · 2023: 3 · 2022: 4 · 2021: 5 · 2020: 3 · 2018: 1
FWCI
1.25
Type
journal article
Language
en
Open access
Locations
  • Journal of Immunology and Regenerative Medicine (publishedVersion)
  • University of Groningen research database (University of Groningen / Centre for Information Technology) (publishedVersion, other-oa)
  • University of Groningen research database (University of Groningen / Centre for Information Technology) (submittedVersion, other-oa)
Funders
  • University Medical Center Groningen
  • China Sponsorship Council (201406630003)
  • UMCG Microscopy and Imaging Center (UMIC) (40-00506-98-9021)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Cellular Mechanics and Interactions
  • Health Sciences › Medicine › Pulmonary and Respiratory Medicine › Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
  • Health Sciences › Medicine › Surgery › Tissue Engineering and Regenerative Medicine
Keywords
macrophage polarization, type I collagen, collagen morphology, extracellular matrix stiffness, pulmonary fibrosis, CD206, Ym1, filopodia, actin cytoskeleton, M2 macrophages, idiopathic pulmonary fibrosis, extracellular matrix mechanics

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