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Bicyclic RGD peptides enhance nerve growth in synthetic PEG-based Anisogels

Nerve regeneration scaffolds often consist of soft hydrogels modified with extracellular matrix (ECM) proteins or fragments, as well as linear and cyclic peptides. One of the commonly used integrin-mediated cell adhesive peptide sequences is Arg-Gly-Asp (RGD). Despite its straightforward coupling me...

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Autores principales: Vedaraman, Sitara, Bernhagen, Dominik, Haraszti, Tamas, Licht, Christopher, Castro Nava, Arturo, Omidinia Anarkoli, Abdolrahman, Timmerman, Peter, De Laporte, Laura
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8204161/
https://www.ncbi.nlm.nih.gov/pubmed/33724266
http://dx.doi.org/10.1039/d0bm02051f
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author Vedaraman, Sitara
Bernhagen, Dominik
Haraszti, Tamas
Licht, Christopher
Castro Nava, Arturo
Omidinia Anarkoli, Abdolrahman
Timmerman, Peter
De Laporte, Laura
author_facet Vedaraman, Sitara
Bernhagen, Dominik
Haraszti, Tamas
Licht, Christopher
Castro Nava, Arturo
Omidinia Anarkoli, Abdolrahman
Timmerman, Peter
De Laporte, Laura
author_sort Vedaraman, Sitara
collection PubMed
description Nerve regeneration scaffolds often consist of soft hydrogels modified with extracellular matrix (ECM) proteins or fragments, as well as linear and cyclic peptides. One of the commonly used integrin-mediated cell adhesive peptide sequences is Arg-Gly-Asp (RGD). Despite its straightforward coupling mechanisms to artificial extracellular matrix (aECM) constructs, linear RGD peptides suffer from low stability towards degradation and lack integrin selectivity. Cyclization of RGD improves the affinity towards integrin subtypes but lacks selectivity. In this study, a new class of short bicyclic peptides with RGD in a cyclic loop and ‘random screened’ tri-amino acid peptide sequences in the second loop is investigated as a biochemical cue for cell growth inside three-dimensional (3D) synthetic poly(ethylene glycol) (PEG)-based Anisogels. These peptides impart high integrin affinity and selectivity towards either α(v)β(3) or α(5)β(1) integrin subunits. Enzymatic conjugation of such bicyclic peptides to the PEG backbone enables the formulation of an aECM hydrogel that supports nerve growth. Furthermore, different proteolytic cleavable moieties are incorporated and compared to promote cell migration and proliferation, resulting in enhanced cell growth with different degradable peptide crosslinkers. Mouse fibroblasts and primary nerve cells from embryonic chick dorsal root ganglions (DRGs) show superior growth in bicyclic RGD peptide conjugated gels selective towards α(v)β(3) or α(5)β(1), compared to monocyclic or linear RGD peptides, with a slight preference to α(v)β(3) selective bicyclic peptides in the case of nerve growth. Synthetic Anisogels, modified with bicyclic RGD peptides and containing short aligned, magneto-responsive fibers, show oriented DRG outgrowth parallel to the fibers. This report shows the potential of PEG hydrogels coupled with bicyclic RGD peptides as an aECM model and paves the way for a new class of integrin selective biomolecules for cell growth and nerve regeneration.
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spelling pubmed-82041612021-06-29 Bicyclic RGD peptides enhance nerve growth in synthetic PEG-based Anisogels Vedaraman, Sitara Bernhagen, Dominik Haraszti, Tamas Licht, Christopher Castro Nava, Arturo Omidinia Anarkoli, Abdolrahman Timmerman, Peter De Laporte, Laura Biomater Sci Chemistry Nerve regeneration scaffolds often consist of soft hydrogels modified with extracellular matrix (ECM) proteins or fragments, as well as linear and cyclic peptides. One of the commonly used integrin-mediated cell adhesive peptide sequences is Arg-Gly-Asp (RGD). Despite its straightforward coupling mechanisms to artificial extracellular matrix (aECM) constructs, linear RGD peptides suffer from low stability towards degradation and lack integrin selectivity. Cyclization of RGD improves the affinity towards integrin subtypes but lacks selectivity. In this study, a new class of short bicyclic peptides with RGD in a cyclic loop and ‘random screened’ tri-amino acid peptide sequences in the second loop is investigated as a biochemical cue for cell growth inside three-dimensional (3D) synthetic poly(ethylene glycol) (PEG)-based Anisogels. These peptides impart high integrin affinity and selectivity towards either α(v)β(3) or α(5)β(1) integrin subunits. Enzymatic conjugation of such bicyclic peptides to the PEG backbone enables the formulation of an aECM hydrogel that supports nerve growth. Furthermore, different proteolytic cleavable moieties are incorporated and compared to promote cell migration and proliferation, resulting in enhanced cell growth with different degradable peptide crosslinkers. Mouse fibroblasts and primary nerve cells from embryonic chick dorsal root ganglions (DRGs) show superior growth in bicyclic RGD peptide conjugated gels selective towards α(v)β(3) or α(5)β(1), compared to monocyclic or linear RGD peptides, with a slight preference to α(v)β(3) selective bicyclic peptides in the case of nerve growth. Synthetic Anisogels, modified with bicyclic RGD peptides and containing short aligned, magneto-responsive fibers, show oriented DRG outgrowth parallel to the fibers. This report shows the potential of PEG hydrogels coupled with bicyclic RGD peptides as an aECM model and paves the way for a new class of integrin selective biomolecules for cell growth and nerve regeneration. The Royal Society of Chemistry 2021-03-16 /pmc/articles/PMC8204161/ /pubmed/33724266 http://dx.doi.org/10.1039/d0bm02051f Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Vedaraman, Sitara
Bernhagen, Dominik
Haraszti, Tamas
Licht, Christopher
Castro Nava, Arturo
Omidinia Anarkoli, Abdolrahman
Timmerman, Peter
De Laporte, Laura
Bicyclic RGD peptides enhance nerve growth in synthetic PEG-based Anisogels
title Bicyclic RGD peptides enhance nerve growth in synthetic PEG-based Anisogels
title_full Bicyclic RGD peptides enhance nerve growth in synthetic PEG-based Anisogels
title_fullStr Bicyclic RGD peptides enhance nerve growth in synthetic PEG-based Anisogels
title_full_unstemmed Bicyclic RGD peptides enhance nerve growth in synthetic PEG-based Anisogels
title_short Bicyclic RGD peptides enhance nerve growth in synthetic PEG-based Anisogels
title_sort bicyclic rgd peptides enhance nerve growth in synthetic peg-based anisogels
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8204161/
https://www.ncbi.nlm.nih.gov/pubmed/33724266
http://dx.doi.org/10.1039/d0bm02051f
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