Insights into the material properties of dragline spider silk affecting Schwann cell migration

  • Aida Naghilou (Corresponding author)
  • , Karolina Peter
  • , Flavia Millesi
  • , Sarah Stadlmayr
  • , Sonja Wolf
  • , Anda Rad
  • , Lorenz Semmler
  • , Paul Supper
  • , Leon Ploszczanski
  • , Jiliang Liu
  • , Manfred Burghammer
  • , Christian Riekel
  • , Alexander Bismarck
  • , Ellen H.G. Backus
  • , Helga Lichtenegger
  • , Christine Radtke

Publications: Contribution to journalArticlePeer Reviewed

Abstract

Dragline silk of Trichonephila spiders has attracted attention in various applications. One of the most fascinating uses of dragline silk is in nerve regeneration as a luminal filling for nerve guidance conduits. In fact, conduits filled with spider silk can measure up to autologous nerve transplantation, but the reasons behind the success of silk fibers are not yet understood. In this study dragline fibers of Trichonephila edulis were sterilized with ethanol, UV radiation, and autoclaving and the resulting material properties were characterized with regard to the silk's suitability for nerve regeneration. Rat Schwann cells (rSCs) were seeded on these silks in vitro and their migration and proliferation were investigated as an indication for the fiber's ability to support the growth of nerves. It was found that rSCs migrate faster on ethanol treated fibers. To elucidate the reasons behind this behavior, the fiber's morphology, surface chemistry, secondary protein structure, crystallinity, and mechanical properties were studied. The results demonstrate that the synergy of dragline silk's stiffness and its composition has a crucial effect on the migration of rSCs. These findings pave the way towards understanding the response of SCs to silk fibers as well as the targeted production of synthetic alternatives for regenerative medicine applications.

Original languageEnglish
Article number125398
JournalInternational Journal of Biological Macromolecules
Volume244
DOIs
Publication statusPublished - 31 Jul 2023

Funding

The authors would like to thank Dr. Stephan Puchegger and the faculty center for nanostructure research at the University of Vienna for support with scanning electron microscopy as well as Professor Bruno K. Podesser and his team at the Center for Biomedical Research, Medical University of Vienna for sharing euthanized rats for tissue harvest. We are grateful for the constant support from Dr. Marion Gröger and her team at the Core Facility Imaging of Medical University of Vienna. The XRD experiments were performed on beamline ID13 at the European Synchrotron Radiation Facility (ESRF), Grenoble, France. We are grateful to Manfred Burghammer at the ESRF for providing assistance in using beamline ID13. We also thank Dr. Robyn Plowright from Newrotex Ltd. for partly providing the silks employed for the revisions. This research is supported by the Austrian Science fund (FWF): project number P 33613. This research is supported by the Austrian Science fund (FWF): project number P 33613 .

Austrian Fields of Science 2012

  • 106002 Biochemistry
  • 106023 Molecular biology
  • 104019 Polymer sciences

Keywords

  • Crystallinity
  • Peripheral nerve regeneration
  • Secondary protein structure
  • Sterilization
  • Stiffness
  • Trichonephila

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