Revitalized and synovialized allograft for intrasynovial flexor tendon reconstruction in an in vivo canine model
ABSTRACT This study was to test our hypothesis that flexor tendon reconstruction with an allograft revitalized with bone marrow stromal cells (BMSCs) and synovialized with carbodiimide derivatized autologous synovial fluid (cd‐SYN) would result in better digit functional restoration than the convent...
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Published in: | Journal of orthopaedic research Vol. 36; no. 8; pp. 2218 - 2227 |
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Abstract | ABSTRACT
This study was to test our hypothesis that flexor tendon reconstruction with an allograft revitalized with bone marrow stromal cells (BMSCs) and synovialized with carbodiimide derivatized autologous synovial fluid (cd‐SYN) would result in better digit functional restoration than the conventional allograft tendon. A total of 32 flexor digital profundus tendons from the second and fifth digit of 16 dogs were created a repair failure model first. Then, failed‐repaired tendons were reconstructed with either a revitalized‐synovialized allograft tendon or a clinical standard autograft tendon (control group). The allograft tendon was seeded with autologous BMSCs in multiple slits and the graft surface was coated with cd‐SYN. A 6 weeks after tendon reconstruction, the digits were harvested and evaluated for digit function, adhesion status, tendon gliding resistance, attachment strength, cell viability, and histologic factors. The allograft group had significantly improved digit function compared with the control group through decreased work of flexion, increased digit range of motion under 2‐Newton force, and less adhesion score (p < .05). However, the distal attachment‐site strength and stiffness in the allograft tendon were significantly weaker than the autografts (p < .05). No significant difference was found for gliding resistance. Histologically, allograft tendons coated with allograft had smoother surfaces and showed tendon‐to‐bone and tendon‐to‐tendon incorporation. Viable BMSCs were found in the tendon slits 6 weeks after the graft. In conclusion, cellular lubricant‐based modification of allograft tendons improved digit function and reduced the adhesions compared with autograft for flexor tendon reconstruction. However, improvement of graft‐to‐host tendon healing is still challenging. © 2018 Orthopaedic Research Society. Published by Wiley Periodicals, Inc. J Orthop Res 36:2218–2227, 2018. |
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AbstractList | This study was to test our hypothesis that flexor tendon reconstruction with an allograft revitalized with bone marrow stromal cells (BMSCs) and synovialized with carbodiimide derivatized autologous synovial fluid (cd-SYN) would result in better digit functional restoration than the conventional allograft tendon. A total of 32 flexor digital profundus tendons from the second and fifth digit of 16 dogs were created a repair failure model first. Then, failed-repaired tendons were reconstructed with either a revitalized-synovialized allograft tendon or a clinical standard autograft tendon (control group). The allograft tendon was seeded with autologous BMSCs in multiple slits and the graft surface was coated with cd-SYN. A 6 weeks after tendon reconstruction, the digits were harvested and evaluated for digit function, adhesion status, tendon gliding resistance, attachment strength, cell viability, and histologic factors. The allograft group had significantly improved digit function compared with the control group through decreased work of flexion, increased digit range of motion under 2-Newton force, and less adhesion score (p < .05). However, the distal attachment-site strength and stiffness in the allograft tendon were significantly weaker than the autografts (p < .05). No significant difference was found for gliding resistance. Histologically, allograft tendons coated with allograft had smoother surfaces and showed tendon-to-bone and tendon-to-tendon incorporation. Viable BMSCs were found in the tendon slits 6 weeks after the graft. In conclusion, cellular lubricant-based modification of allograft tendons improved digit function and reduced the adhesions compared with autograft for flexor tendon reconstruction. However, improvement of graft-to-host tendon healing is still challenging. © 2018 Orthopaedic Research Society. Published by Wiley Periodicals, Inc. J Orthop Res. ABSTRACT This study was to test our hypothesis that flexor tendon reconstruction with an allograft revitalized with bone marrow stromal cells (BMSCs) and synovialized with carbodiimide derivatized autologous synovial fluid (cd‐SYN) would result in better digit functional restoration than the conventional allograft tendon. A total of 32 flexor digital profundus tendons from the second and fifth digit of 16 dogs were created a repair failure model first. Then, failed‐repaired tendons were reconstructed with either a revitalized‐synovialized allograft tendon or a clinical standard autograft tendon (control group). The allograft tendon was seeded with autologous BMSCs in multiple slits and the graft surface was coated with cd‐SYN. A 6 weeks after tendon reconstruction, the digits were harvested and evaluated for digit function, adhesion status, tendon gliding resistance, attachment strength, cell viability, and histologic factors. The allograft group had significantly improved digit function compared with the control group through decreased work of flexion, increased digit range of motion under 2‐Newton force, and less adhesion score (p < .05). However, the distal attachment‐site strength and stiffness in the allograft tendon were significantly weaker than the autografts (p < .05). No significant difference was found for gliding resistance. Histologically, allograft tendons coated with allograft had smoother surfaces and showed tendon‐to‐bone and tendon‐to‐tendon incorporation. Viable BMSCs were found in the tendon slits 6 weeks after the graft. In conclusion, cellular lubricant‐based modification of allograft tendons improved digit function and reduced the adhesions compared with autograft for flexor tendon reconstruction. However, improvement of graft‐to‐host tendon healing is still challenging. © 2018 Orthopaedic Research Society. Published by Wiley Periodicals, Inc. J Orthop Res 36:2218–2227, 2018. |
Author | Lu, Cheng‐Chang Amadio, Peter C. Zhao, Chunfeng Reisdorf, Ramona L. Thoreson, Andrew R. Gingery, Anne Zhang, Tao Moran, Steven L. |
Author_xml | – sequence: 1 givenname: Tao surname: Zhang fullname: Zhang, Tao organization: Jinan Central Hospital – sequence: 2 givenname: Cheng‐Chang surname: Lu fullname: Lu, Cheng‐Chang organization: Mayo Clinic – sequence: 3 givenname: Ramona L. surname: Reisdorf fullname: Reisdorf, Ramona L. organization: Mayo Clinic – sequence: 4 givenname: Andrew R. surname: Thoreson fullname: Thoreson, Andrew R. organization: Mayo Clinic – sequence: 5 givenname: Anne surname: Gingery fullname: Gingery, Anne organization: Mayo Clinic – sequence: 6 givenname: Steven L. surname: Moran fullname: Moran, Steven L. organization: Mayo Clinic – sequence: 7 givenname: Peter C. surname: Amadio fullname: Amadio, Peter C. organization: Mayo Clinic – sequence: 8 givenname: Chunfeng surname: Zhao fullname: Zhao, Chunfeng email: zhaoc@mayo.edu organization: Mayo Clinic |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/29575268$$D View this record in MEDLINE/PubMed |
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CitedBy_id | crossref_primary_10_1002_jor_25678 crossref_primary_10_1016_j_hcl_2022_08_020 crossref_primary_10_3389_fvets_2023_1003993 crossref_primary_10_1097_PRS_0000000000008692 crossref_primary_10_3390_bioengineering9010021 |
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Keywords | bone marrow stromal cells graft tendon repair surface modification |
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Snippet | ABSTRACT
This study was to test our hypothesis that flexor tendon reconstruction with an allograft revitalized with bone marrow stromal cells (BMSCs) and... This study was to test our hypothesis that flexor tendon reconstruction with an allograft revitalized with bone marrow stromal cells (BMSCs) and synovialized... |
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SubjectTerms | bone marrow stromal cells graft surface modification tendon repair |
Title | Revitalized and synovialized allograft for intrasynovial flexor tendon reconstruction in an in vivo canine model |
URI | https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fjor.23889 https://www.ncbi.nlm.nih.gov/pubmed/29575268 https://search.proquest.com/docview/2018662601 |
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