Defining the regenerative effects of native spider silk fibers on primary Schwann cells, sensory neurons, and nerve‐associated fibroblasts

• Published in: The FASEB journal 2021-02, Vol.35 (2), p.e21196-n/a
• Main Authors: Millesi, Flavia, Weiss, Tamara, Mann, Anda, Haertinger, Maximilian, Semmler, Lorenz, Supper, Paul, Pils, Dietmar, Naghilou, Aida, Radtke, Christine
• Format: Article
• Language: English
• Subjects: Animals; Cell Movement; Cells, Cultured; Female; Fibroblasts - drug effects; Fibroblasts - physiology; live cell imaging; Male; migration; Nephila edulis; Nerve Regeneration; Neuronal Outgrowth; peripheral nerve regeneration; proliferation; Rats; Rats, Sprague-Dawley; Schwann Cells - drug effects; Schwann Cells - physiology; Sensory Receptor Cells - drug effects; Sensory Receptor Cells - physiology; Silk - pharmacology; Spiders
• ISSN: 0892-6638; 1530-6860
• DOI: 10.1096/fj.202001447R

The search for a suitable material to promote regeneration after long‐distance peripheral nerve defects turned the spotlight on spider silk. Nerve conduits enriched with native spider silk fibers as internal guiding structures previously demonstrated a regenerative outcome similar to autologous nerve grafts in animal studies. Nevertheless, spider silk is a natural material with associated limitations for clinical use. A promising alternative is the production of recombinant silk fibers that should mimic the outstanding properties of their native counterpart. However, in vitro data on the regenerative features that native silk fibers provide for cells involved in nerve regeneration are scarce. Thus, there is a lack of reference parameters to evaluate whether recombinant silk fiber candidates will be eligible for nerve repair in vivo. To gain insight into the regenerative effect of native spider silk, our study aims to define the behavioral response of primary Schwann cells (SCs), nerve‐associated fibroblasts (FBs), and dorsal root ganglion (DRG) neurons cultured on native dragline silk from the genus Nephila and on laminin coated dishes. The established multi‐color immunostaining panels together with confocal microscopy and live cell imaging enabled the analysis of cell identity, morphology, proliferation, and migration on both substrates in detail. Our findings demonstrated that native spider silk rivals laminin coating as it allowed attachment and proliferation and supported the characteristic behavior of all tested cell types. Axonal out‐growth of DRG neurons occurred along longitudinally aligned SCs that formed sustained bundled structures resembling Bungner bands present in regenerating nerves. The migration of SCs along the silk fibers achieved the reported distance of regenerating axons of about 1 mm per day, but lacked directionality. Furthermore, rFBs significantly reduced the velocity of rSCs in co‐cultures on silk fibers. In summary, this study (a) reveals features recombinant silk must possess and what modifications or combinations could be useful for enhanced nerve repair and (b) provides assays to evaluate the regenerative performance of silk fibers in vitro before being applied as internal guiding structure in nerve conduits in vivo.