Issue 22, 2017

Galactose-functionalised PCL nanofibre scaffolds to attenuate inflammatory action of astrocytes in vitro and in vivo

Abstract

Astrocytes represent an attractive therapeutic target for the treatment of traumatic brain injury in the glial scar, which inhibits functional repair and recovery if persistent. Many biomaterial systems have been investigated for neural tissue engineering applications, including electrospun nanofibres, which are a favourable biomaterial as they can mimic the fibrous architecture of the extracellular matrix, and are conveniently modified to present biologically relevant cues to aid in regeneration. Here, we synthesised a novel galactose-presenting polymer, poly(L-lysine)–lactobionic acid (PLL–LBA), for use in layer-by-layer (LbL) functionalisation of poly(ε-caprolactone) (PCL) nanofibres, to covalently attach galactose moieties to the nanofibre scaffold surface. We have assessed the use of this novel biomaterial system in vitro and in vivo, and have shown, for the first time, the ability of galactose to maintain an attenuated inflammatory profile of astrocytes in culture, and to increase the survival of neurons after traumatic injury, as compared to control PCL nanofibres. This study highlights the importance of galactose in controlling the astrocytic response, and provides a promising biomaterial system to deliver the essential morphological and biological cues to achieve functional repair after traumatic brain injury.

Graphical abstract: Galactose-functionalised PCL nanofibre scaffolds to attenuate inflammatory action of astrocytes in vitro and in vivo

Supplementary files

Article information

Article type
Paper
Submitted
08 Mar 2017
Accepted
07 May 2017
First published
08 May 2017

J. Mater. Chem. B, 2017,5, 4073-4083

Galactose-functionalised PCL nanofibre scaffolds to attenuate inflammatory action of astrocytes in vitro and in vivo

F. L. Maclean, C. L. Lau, S. Ozergun, R. D. O'Shea, C. Cederfur, J. Wang, K. E. Healy, F. R. Walker, D. Tomas, M. K. Horne, P. M. Beart and D. R. Nisbet, J. Mater. Chem. B, 2017, 5, 4073 DOI: 10.1039/C7TB00651A

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