Synthesis and in Vitro Evaluation of Enzymatically Cross-Linked Elastin-Like Polypeptide Gels for Cartilaginous Tissue Repair
Genetically engineered elastin-like polypeptide (ELP) hydrogels offer unique promise as scaffolds for cartilage tissue engineering because of the potential to promote chondrogenesis and to control mechanical properties. In this study, we designed and synthesized ELPs capable of undergoing enzyme- in...
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Published in | Tissue engineering Vol. 11; no. 11-12; pp. 1768 - 1779 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
United States
Mary Ann Liebert, Inc
01.11.2005
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Subjects | |
Online Access | Get full text |
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Summary: | Genetically engineered elastin-like polypeptide (ELP) hydrogels offer unique promise as scaffolds
for cartilage tissue engineering because of the potential to promote chondrogenesis and to control
mechanical properties. In this study, we designed and synthesized ELPs capable of undergoing enzyme-
initiated gelation via tissue transglutaminase, with the ultimate goal of creating an injectable,
in situ
cross-linking scaffold to promote functional cartilage repair. Addition of the enzyme promoted
ELP gel formation and chondrocyte encapsulation in a biocompatible process, which resulted
in cartilage matrix synthesis
in vitro
and the potential to contribute to cartilage mechanical function
in vivo
. A significant increase in the accumulation of sulfated glycosaminoglycans was observed,
and histological sections revealed the accumulation of a cartilaginous matrix rich in type II collagen
and lacking in type I collagen, indicative of hyaline cartilage formation. These results provide
evidence of chondrocytic phenotype maintenance for cells in the ELP hydrogels
in vitro
. In addition,
the dynamic shear moduli of ELP hydrogels seeded with chondrocytes increased from 0.28 to
1.7 kPa during a 4-week culture period. This increase in the mechanical integrity of cross-linked
ELP hydrogels suggests restructuring of the ELP matrix by deposition of functional cartilage extracellular
matrix components. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 1076-3279 1557-8690 |
DOI: | 10.1089/ten.2005.11.1768 |