Abstract

We investigated the reactivity and expression of basal lamina collagen by Schwann cells (SCs) cultivated on a supraorganized bovine-derived collagen substrate. SC cultures were obtained from sciatic nerves of neonatal Sprague-Dawley rats and seeded on 24-well culture plates containing collagen substrate. The homogeneity of the cultures was evaluated with an SC marker antibody (anti-S-100). After 1 week, the cultures were fixed and processed for immunocytochemistry by using antibodies against type IV collagen, S-100 and p75NTR (pan neurotrophin receptor) and for scanning electron microscopy (SEM). Positive labeling with antibodies to the cited molecules was observed, indicating that the collagen substrate stimulates SC alignment and adhesion (collagen IV labeling - organized collagen substrate: 706.33 ± 370.86, non-organized collagen substrate: 744.00 ± 262.09; S-100 labeling - organized collagen: 3809.00 ± 120.28, non-organized collagen: 3026.00 ± 144.63, P < 0.05) and reactivity (p75NTR labeling - organized collagen: 2156.33 ± 561.78, non-organized collagen: 1424.00 ± 405.90, P < 0.05; means ± standard error of the mean in absorbance units). Cell alignment and adhesion to the substrate were confirmed by SEM analysis. The present results indicate that the collagen substrate with an aligned suprastructure, as seen by polarized light microscopy, provides an adequate scaffold for SCs, which in turn may increase the efficiency of the nerve regenerative process after in vivo repair.

Highlights

  • Peripheral nerve regeneration is influenced by the chronology and synchronization of a chain of events following injury

  • The degeneration of the distal stump as well as the sprouting of regenerating fibers are determined by the repair technique, the level of the lesion and the regenerative potential of the axotomized neurons

  • Schwann cells (SCs) are vital elements during the process of peripheral nerve rearrangement following lesion, the so-called Wallerian degeneration. They support the axonal regrowth from the proximal stump, serving as an efficient interface to the extracellular matrix (ECM) [4]

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Summary

Introduction

Peripheral nerve regeneration is influenced by the chronology and synchronization of a chain of events following injury. SCs are vital elements during the process of peripheral nerve rearrangement following lesion, the so-called Wallerian degeneration. They support the axonal regrowth from the proximal stump, serving as an efficient interface to the extracellular matrix (ECM) [4]. In this respect, they express a number of laminins [4,5,6,7] and integrins (e.g., α1β1, α2β1, α6β1) [8] and secrete different neurotrophic factors, including nerve growth factor (NGF), brain-derived neurotrophic factor (BDNF) and the glial-derived neurotrophic factor (GDNF) [9,10]. The SCs organize the so-called bands of Büngner, which provide guidance to the growth cones throughout the distal stump of a lesioned nerve [4,10,11]

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