Bioactive scaffolds with enhanced supramolecular motion promote recovery from spinal cord injury
Motor Neurons
Cell Survival
Polymers
Integrin beta1
Nanofibers
Neovascularization, Physiologic
Recovery of Function
Mice
Neural Stem Cells
Human Umbilical Vein Endothelial Cells
Animals
Humans
Computer Simulation
Protein Conformation, beta-Strand
Laminin
Peptidomimetics
Receptor, Fibroblast Growth Factor, Type 2
Peptides
Spinal Cord Injuries
Signal Transduction
DOI:
10.1126/science.abh3602
Publication Date:
2021-11-11T18:55:42Z
AUTHORS (12)
ABSTRACT
Fibril motion improves peptide signaling
Artificial scaffolds that bear the peptide-signaling sequences of proteins for tissue regeneration often have limited effectiveness. Álvarez
et al
. synthesized supramolecular peptide fibril scaffolds bearing two peptide sequences that promote nerve regeneration, one that reduces glial scarring and another that promotes blood vessel formation (see the Perspective by Wojciechowski and Stevens). In a mouse model of paralyzing human spinal cord injury, mutations in a tetrapeptide domain outside of the signaling regions improved recovery by promoting intense supramolecular motion within the fibrils. The mutation with the most intense dynamics resulted in corticospinal axon regrowth and myelination, functional revascularization, and motor neuron survival. —PDS
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