dc.contributor.author |
Francisco, Aubrey T |
|
dc.contributor.author |
Hwang, Priscilla Y |
|
dc.contributor.author |
Jeong, Claire G |
|
dc.contributor.author |
Jing, Liufang |
|
dc.contributor.author |
Chen, Jun |
|
dc.contributor.author |
Setton, Lori A |
|
dc.date.accessioned |
2014-05-21T15:00:01Z |
|
dc.date.issued |
2014-03-01 |
|
dc.identifier.issn |
1742-7061 |
|
dc.identifier.uri |
https://hdl.handle.net/10161/8876 |
|
dc.description.abstract |
Intervertebral disc (IVD) disorders and age-related degeneration are believed to contribute
to lower back pain. There is significant interest in cell-based strategies for regenerating
the nucleus pulposus (NP) region of the disc; however, few scaffolds have been evaluated
for their ability to promote or maintain an immature NP cell phenotype. Previous studies
have shown that NP cell-laminin interactions promote cell adhesion and biosynthesis,
which suggests a laminin-functionalized biomaterial may be useful for promoting or
maintaining the NP cell phenotype. Here, a photocrosslinkable poly(ethylene glycol)-laminin
111 (PEG-LM111) hydrogel was developed. The mechanical properties of PEG-LM111 hydrogel
could be tuned within the range of dynamic shear moduli values previously reported
for human NP. When primary immature porcine NP cells were seeded onto PEG-LM111 hydrogels
of varying stiffnesses, LM111-presenting hydrogels were found to promote cell clustering
and increased levels of sGAG production as compared to stiffer LM111-presenting and
PEG-only gels. When cells were encapsulated in 3-D gels, hydrogel formulation was
found to influence NP cell metabolism and expression of proposed NP phenotypic markers,
with higher expression of N-cadherin and cytokeratin 8 observed for cells cultured
in softer (<1 kPa) PEG-LM111 hydrogels. Overall, these findings suggest that soft,
LM111-functionalized hydrogels may promote or maintain the expression of specific
markers characteristic of an immature NP cell phenotype. © 2013 Acta Materialia Inc.
Published by Elsevier Ltd. All rights reserved.
|
|
dc.publisher |
Elsevier BV |
|
dc.relation.ispartof |
Acta Biomaterialia |
|
dc.relation.isversionof |
10.1016/j.actbio.2013.11.013 |
|
dc.title |
Photocrosslinkable laminin-functionalized polyethylene glycol hydrogel for intervertebral
disc regeneration
|
|
dc.type |
Journal article |
|
duke.contributor.id |
Chen, Jun|0251573 |
|
duke.contributor.id |
Setton, Lori A|0117045 |
|
pubs.begin-page |
1102 |
|
pubs.end-page |
1111 |
|
pubs.issue |
3 |
|
pubs.organisational-group |
Biomedical Engineering |
|
pubs.organisational-group |
Clinical Science Departments |
|
pubs.organisational-group |
Duke |
|
pubs.organisational-group |
Duke Institute for Brain Sciences |
|
pubs.organisational-group |
Institutes and Provost's Academic Units |
|
pubs.organisational-group |
Orthopaedics |
|
pubs.organisational-group |
Pratt School of Engineering |
|
pubs.organisational-group |
School of Medicine |
|
pubs.organisational-group |
University Institutes and Centers |
|
pubs.publication-status |
Published |
|
pubs.volume |
10 |
|
dc.identifier.eissn |
1878-7568 |
|