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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...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2021
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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. |
format | Online Article Text |
id | pubmed-8204161 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
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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