Journal article
The response of tenocytes to commercial scaffolds used for rotator cuff repair.
- Abstract:
- Surgical repairs of rotator cuff tears have high re-tear rates and many scaffolds have been developed to augment the repair. Understanding the interaction between patients' cells and scaffolds is important for improving scaffold performance and tendon healing. In this in vitro study, we investigated the response of patient-derived tenocytes to eight different scaffolds. Tested scaffolds included X-Repair, Poly-Tape, LARS Ligament, BioFiber (synthetic scaffolds), BioFiber-CM (biosynthetic scaffold), GraftJacket, Permacol, and Conexa (biological scaffolds). Cell attachment, proliferation, gene expression, and morphology were assessed. After one day, more cells attached to synthetic scaffolds with dense, fine and aligned fibres (X-Repair and Poly-Tape). Despite low initial cell attachment, the human dermal scaffold (GraftJacket) promoted the greatest proliferation of cells over 13 days. Expression of collagen types I and III were upregulated in cells grown on non-cross-linked porcine dermis (Conexa). Interestingly, the ratio of collagen I to collagen III mRNA was lower on all dermal scaffolds compared to synthetic and biosynthetic scaffolds. These findings demonstrate significant differences in the response of patient-derived tendon cells to scaffolds that are routinely used for rotator cuff surgery. Synthetic scaffolds promoted increased cell adhesion and a tendon-like cellular phenotype, while biological scaffolds promoted cell proliferation and expression of collagen genes. However, no single scaffold was superior. Our results may help understand the way that patients' cells interact with scaffolds and guide the development of new scaffolds in the future.
- Publication status:
- Published
- Peer review status:
- Peer reviewed
Actions
Access Document
- Files:
-
-
(Preview, Version of record, pdf, 1.6MB, Terms of use)
-
Authors
+ Arthritis Research UK
More from this funder
- Funding agency for:
- Dakin, S
- Snelling, S
- Grant:
- 20506
- 20087
+ NIHR Oxford Biomedical Research Centre
More from this funder
- Funding agency for:
- Smith, R
- Carr, A
- Dakin, S
- Snelling, S
- Hakimi, O
- Grant:
- 20506
- 20087
- Publisher:
- AO Research Institute Davos
- Journal:
- eCells and Materials Journal More from this journal
- Volume:
- 30
- Pages:
- 107-118
- Publication date:
- 2016-01-27
- EISSN:
-
1473-2262
- Language:
-
English
- Keywords:
- Pubs id:
-
pubs:598432
- UUID:
-
uuid:11b776fe-319f-4777-bb81-1a94196a7659
- Local pid:
-
pubs:598432
- Source identifiers:
-
598432
- Deposit date:
-
2016-02-05
- ARK identifier:
Terms of use
- Copyright holder:
- Smith et al
- Copyright date:
- 2016
- Notes:
- Open Access / Author retains copyright. Published by AO Research Institute Davos under license. This is the publisher's version of the article. The final version is available online from AO Research Institute Davos at: [http://www.ecmjournal.org/journal/papers/vol031/vol031a08.php].
If you are the owner of this record, you can report an update to it here: Report update to this record