Characterization of Resilin-Based Materials for Tissue Engineering Applications

被引:71
|
作者
Renner, Julie N. [1 ]
Cherry, Kevin M. [1 ]
Su, Renay S-C. [1 ]
Liu, Julie C. [1 ,2 ]
机构
[1] Purdue Univ, Sch Chem Engn, W Lafayette, IN 47907 USA
[2] Purdue Univ, Weldon Sch Biomed Engn, W Lafayette, IN 47907 USA
基金
美国国家科学基金会;
关键词
ELASTIN-LIKE POLYPEPTIDE; VISCOELASTIC SHEAR PROPERTIES; CELL ATTACHMENT ACTIVITY; MECHANICAL-PROPERTIES; ARTICULAR-CARTILAGE; STEM-CELLS; PROTEIN; RGD; BEHAVIOR; DIFFERENTIATION;
D O I
10.1021/bm301129b
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Modular proteins have emerged :as powerful tools in tissue engineering because both the mechanical and biochemical properties :an: precisely controlled through amino acid:sequence.:Resilin is an attractive candidate for use in modular proteins because it is well known for having low stiffness, high fatigue lifetime, and high, resilience. However, no studies have been conducted to assess resilin's compressive properties, cytocompatibility with clinically relevant cells, or effect On cell spreading. We. designed a modular protein containing repeating sequences of a motif derived from Anopheles gambiae and cell-binding domains derived from fibronectin. Rapid cross linking with tris(hydroxymethyl)phosphine was observed The hydrogels had a complex modulus of 22 +/- 1 kPa and yield strain of 63% The elastic modulus in compression, Or unconfined compressive modulus, was 2.4 +/- 0.2 MPa, which is on the same order as human cartilage. A LIVE/DEAD assay demonstrated that human mesenchymal stem cells cultured on the resilin-based protein had a Viability of 95% after three days. A cell spreading assay revealed that the cells interacted with the fibronectin-derived domain in a sequence specific manner and resulted in a mean cell area similar to 1.4-fold larger than when cells were seeded on a sequence scrambled negative control protein. These results demonstrate that our resilin-based biomaterial is a promising biomaterial for cartilage tissue engineering.
引用
收藏
页码:3678 / 3685
页数:8
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