Cited by 30Tissue Engineering and Regenerative Medicine3D Printing in Biomedical ResearchBone Tissue Engineering Materials

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EDC Cross-linking of Decellularized Tissue: A Promising Approach?

Lehmann, Nadine, Christ, Torsten, Daugs, Aila, Bloch, Oliver, Holinski, Sebastian·2017·Tissue Engineering Part A

Abstract

BACKGROUND: Decellularization of xenogenous cardiovascular structures is a promising approach to create scaffolds for tissue engineering. Unfortunately, handling and pliability of the unfixed tissue is challenging. N-(3-dimethylaminopropyl)-N9-ethylcarbodiimide (EDC) is an alternative cross-linking agent to glutaraldehyde (GA). Applied in native tissue, it provides biocompatibility and shows no potential for calcification. In addition, EDC can be used to link growth factors (GFs) to tissue scaffolds after decellularization. EDC cross-linking could thereby help to improve decellularized tissue without the toxicity of GA. MATERIAL AND METHODS: Porcine aortic wall tissue specimens (TS) were decellularized, treated with EDC, and coated with fibroblast growth factor (FGF) or vascular endothelial growth factor (VEGF). Afterward, TS were subcutaneously implanted in 36 Lewis rats along with one decellularized TS without EDC treatment. After 2, 4, and 6 weeks TS were explanted from 12 rats, respectively. Vital cells were evaluated by RNA quantification, general cellular infiltration by hematoxylin and eosin staining (H&E), macrophage infiltration by CD68 staining, calcification by Von-Kossa staining, and tissue degradation by measurement of TS thickness. RESULTS: Quantification of vital cells showed reduced reseeding of EDC-treated TS compared to noncross-linked TS after 2 (p < 0.05) and 4 weeks (p < 0.05), while after 6 weeks only EDC+VEGF showed fewer viable cells (p < 0.01). Histological evaluation confirmed a reduced infiltration of EDC-treated TS. Macrophage infiltration decreased in all groups from 2 to 6 weeks, with the smallest population in EDC+VEGF-treated TS (p > 0.05). In EDC+FGF-treated TS, macrophages were reduced after 2 weeks compared to noncross-linked TS (p < 0.05), while after 4 and 6 weeks no significant difference was found (p > 0.05). Von-Kossa staining revealed no calcification in any of the specimens. Thickness of noncross-linked and EDC+FGF-treated TS was not different at the respective times of explantation, but decreased in both groups toward 6 weeks. CONCLUSION: EDC cross-linking combined with GF coating of decellularized aortic wall tissue showed encouraging results. The treatment did not impair the advantages of decellularized tissue such as long-term recellularization, absence of calcification, and tissue integrity. Based on the low macrophage infiltration and minimal tissue degradation, treatment with EDC and VEGF could be useful after decellularization. However, further research is necessary to verify these findings in models, including mechanical stress.

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References 37 · Cited by 30

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  1. 10.1089/ten.2006.12.2059 · DOI
  2. 10.12659/MSM.883618 · DOI
  3. 10.1089/ten.tea.2011.0046 · DOI
  4. Dohmen P.M., 2007, J Heart Valve Dis, 16, 447
  5. 10.1159/000091597 · DOI
  6. 10.1016/j.athoracsur.2004.06.033 · DOI
  7. Golomb G., 1987, Am J Pathol, 127, 122
  8. Grabenwöger M., 1996, Surg, 62, 772
  9. 10.1016/0142-9612(96)82721-9 · DOI
  10. Curcio C.A., 1981, J Thorac Cardiovasc Surg, 81, 621, 10.1016/S0022-5223(19)39497-8 · DOI
  11. 10.1093/rb/rbu009 · DOI · Paper page
  12. 10.1016/0003-2697(90)90267-D · DOI
  13. 10.1016/0142-9612(96)81413-X · DOI
  14. 10.1016/S0939-6411(98)00017-4 · DOI
  15. 10.1089/ten.2006.0292 · DOI
  16. Xu X.-F., 2014, Int J Clin Exp Med, 7, 649
  17. 10.5090/kjtcs.2013.46.1.1 · DOI
  18. 10.1016/S0142-9612(00)00164-2 · DOI
  19. 10.1002/jbm.b.31928 · DOI
  20. 10.1111/j.1525-1594.2009.00713.x · DOI
  21. 10.1002/1097-4636(20010605)55:3<368::AID-JBM1025>3.0.CO;2-5 · DOI
  22. 10.1016/S0168-3659(99)00145-5 · DOI
  23. 10.1016/S0142-9612(00)00418-X · DOI
  24. 10.1111/j.1525-1594.2004.00062.x · DOI
  25. 10.1042/BSR20110077 · DOI
  26. 10.4061/2010/218142 · DOI
  27. 10.1152/ajpcell.2001.280.6.C1358 · DOI
  28. Distler J.H.W., 2003, Q J Nucl Med, 47, 149
  29. 10.1002/(SICI)1097-4636(19990605)45:3<209::AID-JBM8>3.0.CO;2-N · DOI
  30. Xu X.-F., 2013, Int J Clin Exp Med, 6, 524
  31. 10.1016/j.trim.2003.12.016 · DOI · Paper page
  32. 10.1016/j.biomaterials.2006.08.022 · DOI
  33. 10.1038/nri1733 · DOI · Paper page
  34. Grabenwöger M., 1992, J Thorac Cardiovasc Surg, 104, 14, 10.1016/S0022-5223(19)34831-7 · DOI
  35. 10.12659/MSMBR.893088 · DOI

Metadata

Authors
Lehmann, N., Christ, T., Daugs, A., Bloch, O., & Holinski, S.
Affiliations
  • Department of Research and Development, AutoTissue Berlin GmbH, Berlin, Germany.
  • Charité – Universitätsmedizin Berlin (DE)
Corresponding author
Christ, Torsten
Venue
Tissue Engineering Part A
Published
2017-07
Volume
23
Issue
13-14
Pages
675-682
ISSN
  • 1937-3341 (ISSN-L)
  • 1937-335X
OpenAlex
W2607629280
Cited by
30
References
37
Citations by year
2026: 1 · 2025: 4 · 2024: 6 · 2023: 5 · 2022: 4 · 2021: 4 · 2020: 4 · 2019: 1 · 2018: 1
FWCI
1.69
Type
journal article
Language
en
Open access
closed
Locations
  • Tissue Engineering Part A (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Health Sciences › Medicine › Surgery › Tissue Engineering and Regenerative Medicine
  • Physical Sciences › Engineering › Biomedical Engineering › 3D Printing in Biomedical Research
  • Physical Sciences › Engineering › Biomedical Engineering › Bone Tissue Engineering Materials
Keywords
decellularized tissue, EDC crosslinking, glutaraldehyde alternative, tissue engineering scaffolds, macrophage infiltration, calcification, reseeding, tissue degradation, xenotransplantation, Lewis rats, tissue engineering, biocompatibility, growth factor delivery
MeSH terms
Animals, Carbodiimides, Cross-Linking Reagents, Fibroblast Growth Factors, Materials Testing, Rats, Inbred Lew, Swine, Coated Materials, Biocompatible, Vascular Endothelial Growth Factor A, Rats, Tissue Scaffolds

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Lehmann, N., Christ, T., Daugs, A., Bloch, O., & Holinski, S. (2017). EDC Cross-linking of Decellularized Tissue: A Promising Approach? Tissue Engineering Part A. https://doi.org/10.1089/ten.tea.2016.0416