IDEAS home Printed from https://ideas.repec.org/a/plo/pone00/0145210.html
   My bibliography  Save this article

Walking the Line: A Fibronectin Fiber-Guided Assay to Probe Early Steps of (Lymph)angiogenesis

Author

Listed:
  • Maria Mitsi
  • Martin Michael Peter Schulz
  • Epameinondas Gousopoulos
  • Alexandra Michaela Ochsenbein
  • Michael Detmar
  • Viola Vogel

Abstract

Angiogenesis and lymphangiogenesis are highly complex morphogenetic processes, central to many physiological and pathological conditions, including development, cancer metastasis, inflammation and wound healing. While it is described that extracellular matrix (ECM) fibers are involved in the spatiotemporal regulation of angiogenesis, current angiogenesis assays are not specifically designed to dissect and quantify the underlying molecular mechanisms of how the fibrillar nature of ECM regulates vessel sprouting. Even less is known about the role of the fibrillar ECM during the early stages of lymphangiogenesis. To address such questions, we introduced here an in vitro (lymph)angiogenesis assay, where we used microbeads coated with endothelial cells as simple sprouting sources and deposited them on single Fn fibers used as substrates to mimic fibrillar ECM. The fibers were deposited on a transparent substrate, suitable for live microscopic observation of the ensuing cell outgrowth events at the single cell level. Our proof-of-concept studies revealed that fibrillar Fn, compared to Fn-coated surfaces, provides far stronger sprouting and guidance cues to endothelial cells, independent of the tested mechanical strains of the Fn fibers. Additionally, we found that VEGF-A, but not VEGF-C, stimulates the collective outgrowth of lymphatic endothelial cells (LEC), while the collective outgrowth of blood vascular endothelial cells (HUVEC) was prominent even in the absence of these angiogenic factors. In addition to the findings presented here, the modularity of our assay allows for the use of different ECM or synthetic fibers as substrates, as well as of other cell types, thus expanding the range of applications in vascular biology and beyond.

Suggested Citation

  • Maria Mitsi & Martin Michael Peter Schulz & Epameinondas Gousopoulos & Alexandra Michaela Ochsenbein & Michael Detmar & Viola Vogel, 2015. "Walking the Line: A Fibronectin Fiber-Guided Assay to Probe Early Steps of (Lymph)angiogenesis," PLOS ONE, Public Library of Science, vol. 10(12), pages 1-28, December.
  • Handle: RePEc:plo:pone00:0145210
    DOI: 10.1371/journal.pone.0145210
    as

    Download full text from publisher

    File URL: https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0145210
    Download Restriction: no

    File URL: https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0145210&type=printable
    Download Restriction: no

    File URL: https://libkey.io/10.1371/journal.pone.0145210?utm_source=ideas
    LibKey link: if access is restricted and if your library uses this service, LibKey will redirect you to where you can use your library subscription to access this item
    ---><---

    References listed on IDEAS

    as
    1. Kristopher E. Kubow & Radmila Vukmirovic & Lin Zhe & Enrico Klotzsch & Michael L. Smith & Delphine Gourdon & Sheila Luna & Viola Vogel, 2015. "Mechanical forces regulate the interactions of fibronectin and collagen I in extracellular matrix," Nature Communications, Nature, vol. 6(1), pages 1-11, November.
    2. Mamta Chabria & Samuel Hertig & Michael L. Smith & Viola Vogel, 2010. "Stretching fibronectin fibres disrupts binding of bacterial adhesins by physically destroying an epitope," Nature Communications, Nature, vol. 1(1), pages 1-9, December.
    Full references (including those not matched with items on IDEAS)

    Most related items

    These are the items that most often cite the same works as this one and are cited by the same works as this one.
    1. Wenjiang Ma & Hanqing Ma & Deane F Mosher, 2015. "On-Off Kinetics of Engagement of FNI Modules of Soluble Fibronectin by β-Strand Addition," PLOS ONE, Public Library of Science, vol. 10(4), pages 1-17, April.
    2. Yuhang Zhang & Jingyi Du & Xian Liu & Fei Shang & Yunxin Deng & Jiaqing Ye & Yukai Wang & Jie Yan & Hu Chen & Miao Yu & Shimin Le, 2024. "Multi-domain interaction mediated strength-building in human α-actinin dimers unveiled by direct single-molecule quantification," Nature Communications, Nature, vol. 15(1), pages 1-17, December.
    3. Sebastien J. P. Callens & Daniel Fan & Ingmar A. J. Hengel & Michelle Minneboo & Pedro J. Díaz-Payno & Molly M. Stevens & Lidy E. Fratila-Apachitei & Amir A. Zadpoor, 2023. "Emergent collective organization of bone cells in complex curvature fields," Nature Communications, Nature, vol. 14(1), pages 1-19, December.

    More about this item

    Statistics

    Access and download statistics

    Corrections

    All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:plo:pone00:0145210. See general information about how to correct material in RePEc.

    If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.

    If CitEc recognized a bibliographic reference but did not link an item in RePEc to it, you can help with this form .

    If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.

    For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: plosone (email available below). General contact details of provider: https://journals.plos.org/plosone/ .

    Please note that corrections may take a couple of weeks to filter through the various RePEc services.

    IDEAS is a RePEc service. RePEc uses bibliographic data supplied by the respective publishers.