| Literature DB >> 27171575 |
Yoshifumi Harada1, Yutaka Mifune1, Atsuyuki Inui1, Ryosuke Sakata1, Tomoyuki Muto1, Fumiaki Takase1, Yasuhiro Ueda1, Takeshi Kataoka1, Takeshi Kokubu1, Ryosuke Kuroda1, Masahiro Kurosaka1.
Abstract
To achieve biological regeneration of tendon-bone junctions, cell sheets of human rotator-cuff derived cells were used in a rat rotator cuff injury model. Human rotator-cuff derived cells were isolated, and cell sheets were made using temperature-responsive culture plates. Infraspinatus tendons in immunodeficient rats were resected bilaterally at the enthesis. In right shoulders, infraspinatus tendons were repaired by the transosseous method and covered with the cell sheet (sheet group), whereas the left infraspinatus tendons were repaired in the same way without the cell sheet (control group). Histological examinations (safranin-O and fast green staining, isolectin B4, type II collagen, and human-specific CD31) and mRNA expression (vascular endothelial growth factor; VEGF, type II collagen; Col2, and tenomodulin; TeM) were analyzed 4 weeks after surgery. Biomechanical tests were performed at 8 weeks. In the sheet group, proteoglycan at the enthesis with more type II collagen and isolectin B4 positive cells were seen compared with in the control group. Human specific CD31-positive cells were detected only in the sheet group. VEGF and Col2 gene expressions were higher and TeM gene expression was lower in the sheet group than in the control group. In mechanical testing, the sheet group showed a significantly higher ultimate failure load than the control group at 8 weeks. Our results indicated that the rotator-cuff derived cell sheet could promote cartilage regeneration and angiogenesis at the enthesis, with superior mechanical strength compared with the control. Treatment for rotator cuff injury using cell sheets could be a promising strategy for enthesis of tendon tissue engineering.Entities:
Keywords: cell sheet; enthesis; rotator cuff repair; rotator cuff-derived cells
Mesh:
Year: 2016 PMID: 27171575 DOI: 10.1002/jor.23289
Source DB: PubMed Journal: J Orthop Res ISSN: 0736-0266 Impact factor: 3.494