Schwann cells (SC), forming bands of Büngner, support and promote axonal outgrowth leading to target reinnervation during nerve regeneration. In order to enhance SC adhesion, proliferation, migration and axonal outgrowth a number of bio-mimetic materials have been studied. Appropriate fibrous substrates, functioning as a temporary extracellular-matrix, can be easily prepared by electrospinning technique, which allows the obtainment fibrous matrices suitable as internal filler for nerve guidance channels to be applied in peripheral nerve repair. Gelatin micro or nano-fibres have been prepared by electrospinning technique by tuning gelatin concentration and solution flow rate. The influence of gelatine fibre diameter on cell adhesion and proliferation, was tested in vitro by using SC and Dorsal Root Ganglia (DRG) explant cultures. Cell adhesion was evaluated by quantifying cell spreading area, actin cytoskeleton organization and focal adhesion complex formation. Nano-fibres have been shown to promote cell spreading and actin cytoskeleton organization, resulting in higher cellular adhesion and proliferation rate in comparison to micro-fibres. Cell migration and motility were quantified by transwell and time lapse assays respectively. Cells cultured on micro-fibres displayed higher motility and migration rate in comparison to nano-fibres. Finally, axonal outgrowth evaluated by culturing DRG explants on the different fibres resulted in higher axonal outgrowth on micro-fibres in comparison to nano-fibres. These data provide a better understanding about glial cell and neuritis viability and organization on gelatin electrospun nano- and micro-fibres suggesting that micro-fibres can be a better filler to be used in the design of new device for peripheral nerve repair applications.

Influence of gelatin fibre diameter on Schwann cell behaviour and axonal outgrowth

FORNASARI, BENEDETTA ELENA;CIPRIANI, ELISA;ZANETTI, Marco;PERROTEAU, Isabelle;GEUNA, Stefano;GNAVI, SARA
2014-01-01

Abstract

Schwann cells (SC), forming bands of Büngner, support and promote axonal outgrowth leading to target reinnervation during nerve regeneration. In order to enhance SC adhesion, proliferation, migration and axonal outgrowth a number of bio-mimetic materials have been studied. Appropriate fibrous substrates, functioning as a temporary extracellular-matrix, can be easily prepared by electrospinning technique, which allows the obtainment fibrous matrices suitable as internal filler for nerve guidance channels to be applied in peripheral nerve repair. Gelatin micro or nano-fibres have been prepared by electrospinning technique by tuning gelatin concentration and solution flow rate. The influence of gelatine fibre diameter on cell adhesion and proliferation, was tested in vitro by using SC and Dorsal Root Ganglia (DRG) explant cultures. Cell adhesion was evaluated by quantifying cell spreading area, actin cytoskeleton organization and focal adhesion complex formation. Nano-fibres have been shown to promote cell spreading and actin cytoskeleton organization, resulting in higher cellular adhesion and proliferation rate in comparison to micro-fibres. Cell migration and motility were quantified by transwell and time lapse assays respectively. Cells cultured on micro-fibres displayed higher motility and migration rate in comparison to nano-fibres. Finally, axonal outgrowth evaluated by culturing DRG explants on the different fibres resulted in higher axonal outgrowth on micro-fibres in comparison to nano-fibres. These data provide a better understanding about glial cell and neuritis viability and organization on gelatin electrospun nano- and micro-fibres suggesting that micro-fibres can be a better filler to be used in the design of new device for peripheral nerve repair applications.
2014
9th FENS FORUM OF NEUROSCIENCE
Milan, Italy
5-9 luglio
9th FENS FORUM OF NEUROSCIENCE
290
290
http://fens2014.neurosciences.asso.fr/
B.E.Fornasari; C.Tonda-Turo; E. Cipriani; M. Zanetti; G. Ciardelli; I. Perroteau; S. Geuna; S. Gnavi
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2318/154448
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