Biological Evaluation of Acellular Cartilaginous and Dermal Matrixes as Tissue Engineering Scaffolds for Cartilage Regeneration.
Biological Evaluation of Acellular Cartilaginous and Dermal Matrixes as Tissue Engineering Scaffolds for Cartilage Regeneration.
复制标题
脱细胞软骨和真皮基质作为软骨再生组织工程支架的生物学评价
DOI:
10.3389/fcell.2020.624337
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发表时间:
2020
影响因子:
5.5
通讯作者:
Cao Y
中科院分区:
文献类型:
--
作者:
Wang Y;Xu Y;Zhou G;Liu Y;Cao Y
An acellular matrix (AM) as a kind of natural biomaterial is gaining increasing attention in tissue engineering applications. An acellular cartilaginous matrix (ACM) and acellular dermal matrix (ADM) are two kinds of the most widely used AMs in cartilage tissue engineering. However, there is still debate over which of these AMs achieves optimal cartilage regeneration, especially in immunocompetent large animals. In the current study, we fabricated porous ADM and ACM scaffolds by a freeze-drying method and confirmed that ADM had a larger pore size than ACM. By recolonization with goat auricular chondrocytes and in vitro culture, ADM scaffolds exhibited a higher cell adhesion rate, more homogeneous chondrocyte distribution, and neocartilage formation compared with ACM. Additionally, quantitative polymerase chain reaction (qPCR) indicated that expression of cartilage-related genes, including ACAN, COLIIA1, and SOX9, was significantly higher in the ADM group than the ACM group. Furthermore, after subcutaneous implantation in a goat, histological evaluation showed that ADM achieved more stable and matured cartilage compared with ACM, which was confirmed by quantitative data including the wet weight, volume, and contents of DNA, GAG, total collagen, and collagen II. Additionally, immunological assessment suggested that ADM evoked a low immune response compared with ACM as evidenced by qPCR and immunohistochemical analyses of CD3 and CD68, and TUNEL. Collectively, our results indicate that ADM is a more suitable AM for cartilage regeneration, which can be used for cartilage regeneration in immunocompetent large animals.
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影响因子:
3.3
作者:
Schwarz, Silke;Elsaesser, Alexander F.;Rotter, Nicole
通讯作者:
Rotter, Nicole
影响因子:
4.1
作者:
Schwarz, Silke;Koerber, Ludwig;Rotter, Nicole
通讯作者:
Rotter, Nicole
影响因子:
--
作者:
Rotter, N;Ung, F;Bonassar, LJ
通讯作者:
Bonassar, LJ
影响因子:
--
作者:
Shakya, Akhilesh Kumar;Nandakumar, Kutty Selva
通讯作者:
Nandakumar, Kutty Selva
影响因子:
5.6
作者:
Ma, Anlun;Jiang, Li;Chen, Huifang
通讯作者:
Chen, Huifang