Title of article :
Relationship between scaffold channel diameter and number of regenerating axons in the transected rat spinal cord
Author/Authors :
Krych، نويسنده , , Aaron J. and Rooney، نويسنده , , Gemma E. and Chen، نويسنده , , Bingkun and Schermerhorn، نويسنده , , Thomas C. and Ameenuddin، نويسنده , , Syed and Gross، نويسنده , , LouAnn and Moore، نويسنده , , Michael J. and Currier، نويسنده , , Bradford L. and Spinner، نويسنده , , Robert J. and Friedman، نويسنده , , Jonathan A. and Yaszemski، نويسنده , , Michael J. and Windebank، نويسنده , , Anthony J.، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2009
Pages :
9
From page :
2551
To page :
2559
Abstract :
Regeneration of endogenous axons through a Schwann cell (SC)-seeded scaffold implant has been demonstrated in the transected rat spinal cord. The formation of a cellular lining in the scaffold channel may limit the degree of axonal regeneration. Spinal cords of adult rats were transected and implanted with the SC-loaded polylactic co-glycollic acid (PLGA) scaffold implants containing seven parallel-aligned channels, either 450 μm (n = 19) or 660 μm in diameter (n = 14). Animals were sacrificed after 1, 2 and 3 months. Immunohistochemistry for neurofilament expression was performed. The cross-sectional area of fibrous tissue and regenerative core was calculated. We found that the 450 μm scaffolds had significantly greater axon fibers per channel at the 1 month (186 ± 37) and 3 month (78 ± 11) endpoints than the 660 μm scaffolds (90 ± 19 and 40 ± 6, respectively) (p = 0.0164 and 0.0149, respectively). The difference in the area of fibrous rim between the 450 and 660 μm channels was most pronounced at the 1 month endpoint, at 28,046 ± 6551 and 58,633 ± 7063 μm2, respectively (p = 0.0105). Our study suggests that fabricating scaffolds with smaller diameter channels promotes greater regeneration over larger diameter channels. Axonal regeneration was reduced in the larger channels due to the generation of a large fibrous rim. Optimization of this scaffold environment establishes a platform for future studies of the effects of cell types, trophic factors or pharmacological agents on the regenerative capacity of the injured spinal cord.
Keywords :
Central nervous system , Polymeric scaffolds , BIOMEDICAL ENGINEERING , Tissue development and growth
Journal title :
Acta Biomaterialia
Serial Year :
2009
Journal title :
Acta Biomaterialia
Record number :
1753234
Link To Document :
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