Exploiting Differential Surface Display of Chondroitin Sulfate Variants for Directing Neuronal Outgrowth

Chondroitin sulfate (CS) proteoglycans (CSPGs) are known to be primary inhibitors of neuronal regeneration at scar sites. However, a variety of CSPGs are also involved in neuronal growth and guidance during other physiological stages. Sulfation patterns of CS chains influence their interactions with...

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Bibliographic Details
Published in:Journal of the American Chemical Society 2013-09, Vol.135 (36), p.13488-13494
Main Authors: Swarup, Vimal P., Hsiao, Tony W., Zhang, Jianxing, Prestwich, Glenn D., Kuberan, Balagurunathan, Hlady, Vladimir
Format: Article
Language:English
Subjects:
Animals
Cell Growth Processes - drug effects
Cells, Cultured
Chondroitin Sulfates - chemistry
Chondroitin Sulfates - pharmacology
Molecular Structure
Neurons - cytology
Neurons - drug effects
Rats
Structure-Activity Relationship
Surface Properties
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Summary:Chondroitin sulfate (CS) proteoglycans (CSPGs) are known to be primary inhibitors of neuronal regeneration at scar sites. However, a variety of CSPGs are also involved in neuronal growth and guidance during other physiological stages. Sulfation patterns of CS chains influence their interactions with various growth factors in the central nervous system (CNS), thus influencing neuronal growth, inhibition, and pathfinding. This report demonstrates the use of differentially sulfated CS chains for neuronal navigation. Surface-immobilized patterns of CS glycosaminoglycan chains were used to determine neuronal preference toward specific sulfations of five CS variants: CS-A, CS-B (dermatan sulfate), CS-C, CS-D, and CS-E. Neurons preferred CS-A, CS-B, and CS-E and avoided CS-C containing lanes. In addition, significant alignment of neurites was observed using underlying lanes containing CS-A, CS-B, and CS-E chains. To utilize differential preference of neurons toward the CS variants, a binary combinations of CS chains were created by backfilling a neuro-preferred CS variant between the microcontact printed lanes of CS-C stripes, which are avoided by neurons. The neuronal outgrowth results demonstrate for the first time that a combination of sulfation variants of CS chains without any protein component of CSPG is sufficient for directing neuronal outgrowth. Biomaterials with surface immobilized GAG chains could find numerous applications as bridging devices for tackling CNS injuries where directional growth of neurons is critical for recovery.
ISSN:0002-7863
1520-5126
DOI:10.1021/ja4056728