TY - JOUR
T1 - Delivery of Brain-Derived Neurotrophic Factor by 3D Biocompatible Polymeric Scaffolds for Neural Tissue Engineering and Neuronal Regeneration
AU - Limongi, Tania
AU - Rocchi, A.
AU - Cesca, F.
AU - Tan, H.
AU - Miele, E.
AU - Giugni, Andrea
AU - Orlando, M.
AU - Perrone Donnorso, M.
AU - Perozziello, G.
AU - Benfenati, Fabio
AU - Di Fabrizio, Enzo M.
N1 - KAUST Repository Item: Exported on 2020-10-01
Acknowledgements: The work was supported by the King Abdullah University of Science and Technology start-up funding and by research grants from the European Union FP7 BNeuroscaffolds^ (grant number 604263 to FB), Compagnia di San Paolo-Italy (to FC).
PY - 2018/3/29
Y1 - 2018/3/29
N2 - Biopolymers are increasingly employed for neuroscience applications as scaffolds to drive and promote neural regrowth, thanks to their ability to mediate the upload and subsequent release of active molecules and drugs. Synthetic degradable polymers are characterized by different responses ranging from tunable distension or shrinkage to total dissolution, depending on the function they are designed for. In this paper we present a biocompatible microfabricated poly-ε-caprolactone (PCL) scaffold for primary neuron growth and maturation that has been optimized for the in vitro controlled release of brain-derived neurotrophic factor (BDNF). We demonstrate that the designed morphology confers to these devices an enhanced drug delivery capability with respect to monolithic unstructured supports. After incubation with BDNF, micropillared PCL devices progressively release the neurotrophin over 21 days in vitro. Moreover, the bioactivity of released BDNF is confirmed using primary neuronal cultures, where it mediates a consistent activation of BDNF signaling cascades, increased synaptic density, and neuronal survival. These results provide the proof-of-principle on the fabrication process of micropatterned PCL devices, which represent a promising therapeutic option to enhance neuronal regeneration after lesion and for neural tissue engineering and prosthetics.
AB - Biopolymers are increasingly employed for neuroscience applications as scaffolds to drive and promote neural regrowth, thanks to their ability to mediate the upload and subsequent release of active molecules and drugs. Synthetic degradable polymers are characterized by different responses ranging from tunable distension or shrinkage to total dissolution, depending on the function they are designed for. In this paper we present a biocompatible microfabricated poly-ε-caprolactone (PCL) scaffold for primary neuron growth and maturation that has been optimized for the in vitro controlled release of brain-derived neurotrophic factor (BDNF). We demonstrate that the designed morphology confers to these devices an enhanced drug delivery capability with respect to monolithic unstructured supports. After incubation with BDNF, micropillared PCL devices progressively release the neurotrophin over 21 days in vitro. Moreover, the bioactivity of released BDNF is confirmed using primary neuronal cultures, where it mediates a consistent activation of BDNF signaling cascades, increased synaptic density, and neuronal survival. These results provide the proof-of-principle on the fabrication process of micropatterned PCL devices, which represent a promising therapeutic option to enhance neuronal regeneration after lesion and for neural tissue engineering and prosthetics.
UR - http://hdl.handle.net/10754/627626
UR - http://link.springer.com/article/10.1007/s12035-018-1022-z
UR - http://www.scopus.com/inward/record.url?scp=85044524412&partnerID=8YFLogxK
U2 - 10.1007/s12035-018-1022-z
DO - 10.1007/s12035-018-1022-z
M3 - Article
C2 - 29600349
SN - 0893-7648
VL - 55
SP - 8788
EP - 8798
JO - Molecular Neurobiology
JF - Molecular Neurobiology
IS - 12
ER -