Evaluation of bone matrix gelatin/fibrin glue and chitosan/gelatin composite scaffolds for cartilage tissue engineering

被引:8
|
作者
Wang, Z. H. [1 ]
Zhang, J. [2 ]
Zhang, Q. [1 ]
Gao, Y. [1 ]
Yan, J. [1 ]
Zhao, X. Y. [1 ]
Yang, Y. Y. [1 ]
Kong, D. M. [1 ]
Zhao, J. [1 ]
Shi, Y. X. [1 ]
Li, X. L. [3 ]
机构
[1] Xi An Jiao Tong Univ, Hosp 2, Dept Otolaryngol Head & Neck Surg, Xian, Peoples R China
[2] Yanan Univ, Affiliated Hosp, Dept Otolaryngol, Yanan, Peoples R China
[3] Xi An Jiao Tong Univ, Hosp 2, Dept Dermatol, Xian, Peoples R China
基金
中国国家自然科学基金;
关键词
Chondrocyte; Tissue engineering; Composite scaffold; Bone matrix; Cartilage; Chitosan; FIBRIN GLUE; IN-VITRO;
D O I
10.4238/gmr.15038431
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
This study was designed to evaluate bone matrix gelatin (BMG)/fibrin glue and chitosan/gelatin composite scaffolds for cartilage tissue engineering. Chondrocytes were isolated from costal cartilage of Sprague-Dawley rats and seeded on BMG/fibrin glue or chitosan/gelatin composite scaffolds. After different in vitro culture durations, the scaffolds were subjected to hematoxylin and eosin, Masson's trichrome, and toluidine blue staining, anti-collagen II and anti-aggrecan immunohistochemistry, and scanning electronic microscopy (SEM) analysis. After 2 weeks of culture, chondrocytes were distributed evenly on the surfaces of both scaffolds. Cell numbers and the presence of extracellular matrix components were markedly increased after 8 weeks of culture, and to a greater extent on the chitosan/gelatin scaffold. The BMG/fibrin glue scaffold showed signs of degradation after 8 weeks. Immunofluorescence analysis confirmed higher levels of collagen II and aggrecan using the chitosan/gelatin scaffold. SEM revealed that the majority of cells on the surface of the BMG/fibrin glue scaffold demonstrated a round morphology, while those in the chitosan/gelatin group had a spindle-like shape, with pseudopodia. Chitosan/gelatin scaffolds appear to be superior to BMG/fibrin glue constructs in supporting chondrocyte attachment, proliferation, and biosynthesis of cartilaginous matrix components.
引用
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页数:8
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