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Tytuł pozycji:

Histological, Biomechanical, and Biological Properties of Genipin-Crosslinked Decellularized Peripheral Nerves.

Tytuł:
Histological, Biomechanical, and Biological Properties of Genipin-Crosslinked Decellularized Peripheral Nerves.
Autorzy:
García-García ÓD; Tissue Engineering Group, Department of Histology, University of Granada, 18016 Granada, Spain.; Instituto de Investigación Biosanitaria ibs. GRANADA, 18012 Granada, Spain.; Doctoral Program in Biomedicine, University of Granada, 18012 Granada, Spain.
El Soury M; Tissue Engineering Group, Department of Histology, University of Granada, 18016 Granada, Spain.; Department of Clinical and Biological Sciences and Neuroscience Institute Cavalieri Ottolenghi (NICO), University of Torino, 10043 Orbassano, Italy.
González-Quevedo D; Tissue Engineering Group, Department of Histology, University of Granada, 18016 Granada, Spain.; Department of Orthopedic Surgery and Traumatology, Regional University Hospital of Málaga, 29010 Málaga, Spain.
Sánchez-Porras D; Tissue Engineering Group, Department of Histology, University of Granada, 18016 Granada, Spain.; Instituto de Investigación Biosanitaria ibs. GRANADA, 18012 Granada, Spain.
Chato-Astrain J; Tissue Engineering Group, Department of Histology, University of Granada, 18016 Granada, Spain.; Instituto de Investigación Biosanitaria ibs. GRANADA, 18012 Granada, Spain.
Campos F; Tissue Engineering Group, Department of Histology, University of Granada, 18016 Granada, Spain.; Instituto de Investigación Biosanitaria ibs. GRANADA, 18012 Granada, Spain.
Carriel V; Tissue Engineering Group, Department of Histology, University of Granada, 18016 Granada, Spain.; Instituto de Investigación Biosanitaria ibs. GRANADA, 18012 Granada, Spain.
Źródło:
International journal of molecular sciences [Int J Mol Sci] 2021 Jan 12; Vol. 22 (2). Date of Electronic Publication: 2021 Jan 12.
Typ publikacji:
Journal Article
Język:
English
Imprint Name(s):
Original Publication: Basel, Switzerland : MDPI, [2000-
MeSH Terms:
Nerve Tissue*/cytology
Nerve Tissue*/ultrastructure
Biocompatible Materials/*chemistry
Iridoids/*chemistry
Tissue Scaffolds/*chemistry
Biomechanical Phenomena ; Cross-Linking Reagents ; Extracellular Matrix/chemistry ; Extracellular Matrix/ultrastructure ; Histocytochemistry ; Nerve Regeneration ; Tissue Engineering
References:
Ann Biomed Eng. 2018 Nov;46(11):1921-1937. (PMID: 29987538)
Methods Mol Biol. 2017;1560:207-218. (PMID: 28155156)
Histochem Cell Biol. 2011 Dec;136(6):709-17. (PMID: 22038043)
Front Cell Neurosci. 2018 Nov 19;12:427. (PMID: 30510503)
J Biomed Mater Res B Appl Biomater. 2015 Aug;103(6):1188-97. (PMID: 25308088)
Bone Joint J. 2020 Aug;102-B(8):1095-1106. (PMID: 32731821)
Nanomedicine (Lond). 2019 Oct;14(20):2763-2775. (PMID: 31612774)
Mol Vis. 2019 Oct 06;25:574-582. (PMID: 31673223)
Plast Reconstr Surg. 2001 May;107(6):1419-29. (PMID: 11335811)
Sci Rep. 2019 Jul 23;9(1):10674. (PMID: 31337821)
Histochem Cell Biol. 2018 Oct;150(4):379-393. (PMID: 29931444)
J Neural Eng. 2018 Apr;15(2):021003. (PMID: 29244032)
Biomed Mater. 2019 Dec 09;15(1):015008. (PMID: 31665713)
Tissue Eng Regen Med. 2018 Dec 8;16(1):39-50. (PMID: 30815349)
Glia. 2008 Nov 1;56(14):1498-507. (PMID: 18803319)
J Reconstr Microsurg. 2013 Oct;29(8):517-22. (PMID: 23818251)
Ann Biomed Eng. 2016 Sep;44(9):2827-39. (PMID: 26842626)
Transl Vis Sci Technol. 2015 Apr 10;4(2):13. (PMID: 25909036)
Adv Biosyst. 2020 Mar;4(3):e1900212. (PMID: 32293152)
J Biomater Sci Polym Ed. 2018 Dec;29(17):2051-2067. (PMID: 29983100)
Expert Rev Neurother. 2014 Mar;14(3):301-18. (PMID: 24506662)
Mater Sci Eng C Mater Biol Appl. 2013 Aug 1;33(6):3514-21. (PMID: 23706241)
Front Med. 2015 Dec;9(4):401-11. (PMID: 26482066)
Muscle Nerve. 2000 Jun;23(6):863-73. (PMID: 10842261)
J Tissue Eng Regen Med. 2017 May;11(5):1412-1426. (PMID: 26177604)
Biomed Mater. 2018 Feb 08;13(2):025021. (PMID: 29420310)
Microsurgery. 2010 Jul;30(5):414-6. (PMID: 20017202)
Plast Reconstr Surg. 1988 Dec;82(6):1052-66. (PMID: 3264409)
Cell Tissue Bank. 2018 Sep;19(3):311-321. (PMID: 29222694)
J Biomed Mater Res. 1998 Dec 15;42(4):560-7. (PMID: 9827680)
Brain Res. 1998 Jun 8;795(1-2):44-54. (PMID: 9622591)
J Orthop Res. 2017 Sep;35(9):1949-1957. (PMID: 27859554)
Methods Mol Biol. 2017;1560:197-206. (PMID: 28155155)
Int J Mol Sci. 2020 Sep 17;21(18):. (PMID: 32957651)
Muscle Nerve. 2011 Aug;44(2):221-34. (PMID: 21660979)
Eur J Pharmacol. 2004 Jul 14;495(2-3):201-8. (PMID: 15249171)
Biomaterials. 2006 Jul;27(19):3675-83. (PMID: 16519932)
Biomed Mater. 2016 Sep 29;11(5):055004. (PMID: 27680194)
Methods. 2020 Jan 15;171:41-61. (PMID: 31398392)
J Biomed Mater Res. 2001 Jun 15;55(4):576-86. (PMID: 11288086)
Nanoscale. 2016 Apr 21;8(15):8138-50. (PMID: 27029891)
Tissue Antigens. 2012 Aug;80(2):165-74. (PMID: 22631597)
Scand J Surg. 2008;97(4):310-6. (PMID: 19211385)
J Tissue Eng Regen Med. 2020 Jun;14(6):789-806. (PMID: 32293801)
Curr Protein Pept Sci. 2017;18(9):946-955. (PMID: 27455969)
Biomaterials. 2000 Nov;21(22):2215-31. (PMID: 11026628)
Biomaterials. 2020 Sep;254:120109. (PMID: 32480093)
Front Cell Neurosci. 2018 Dec 18;12:501. (PMID: 30627086)
Methods. 2015 Aug;84:25-34. (PMID: 25791470)
Exp Eye Res. 2019 Sep;186:107717. (PMID: 31265829)
Acta Biomater. 2020 Oct 1;115:235-249. (PMID: 32771587)
Carbohydr Polym. 2014 Feb 15;102:901-11. (PMID: 24507362)
J R Soc Interface. 2012 Feb 7;9(67):202-21. (PMID: 22090283)
Biomaterials. 2008 Jul;29(20):2941-53. (PMID: 18440630)
Eur J Cardiothorac Surg. 2003 Jun;23(6):1002-6; discussion 1006. (PMID: 12829079)
J Tissue Eng Regen Med. 2017 Feb;11(2):553-563. (PMID: 25080900)
Acta Biomater. 2020 Oct 1;115:51-59. (PMID: 32771593)
Front Bioeng Biotechnol. 2020 Jun 16;8:596. (PMID: 32612984)
Int Rev Neurobiol. 2009;87:27-46. (PMID: 19682632)
J Food Drug Anal. 2017 Jan;25(1):43-61. (PMID: 28911543)
Injury. 2012 May;43(5):553-72. (PMID: 21269624)
Biomaterials. 2011 Apr;32(12):3233-43. (PMID: 21296410)
Muscle Nerve. 2009 Jun;39(6):787-99. (PMID: 19291791)
Hand (N Y). 2010 Sep;5(3):273-7. (PMID: 19937145)
J Anat. 2006 Oct;209(4):511-26. (PMID: 17005023)
Cell Tissue Bank. 2014 Dec;15(4):531-41. (PMID: 24442821)
J Neural Eng. 2013 Apr;10(2):026022. (PMID: 23528562)
Grant Information:
PI17-0393 Instituto de Salud Carlos III; FIS PI20-0318 Instituto de Salud Carlos III
Contributed Indexing:
Keywords: biomechanical and structural properties; cell-biomaterials interactions; chemical crosslinking; genipin; histology; natural biomaterials; nerve repair; nerve tissue decellularization; tissue engineering
Substance Nomenclature:
0 (Biocompatible Materials)
0 (Cross-Linking Reagents)
0 (Iridoids)
A3V2NE52YG (genipin)
Entry Date(s):
Date Created: 20210115 Date Completed: 20210412 Latest Revision: 20210412
Update Code:
20240105
PubMed Central ID:
PMC7826762
DOI:
10.3390/ijms22020674
PMID:
33445493
Czasopismo naukowe
Acellular nerve allografts (ANGs) represent a promising alternative in nerve repair. Our aim is to improve the structural and biomechanical properties of biocompatible Sondell (SD) and Roosens (RS) based ANGs using genipin (GP) as a crosslinker agent ex vivo. The impact of two concentrations of GP (0.10% and 0.25%) on Wistar rat sciatic nerve-derived ANGs was assessed at the histological, biomechanical, and biocompatibility levels. Histology confirmed the differences between SD and RS procedures, but not remarkable changes were induced by GP, which helped to preserve the nerve histological pattern. Tensile test revealed that GP enhanced the biomechanical properties of SD and RS ANGs, being the crosslinked RS ANGs more comparable to the native nerves used as control. The evaluation of the ANGs biocompatibility conducted with adipose-derived mesenchymal stem cells cultured within the ANGs confirmed a high degree of biocompatibility in all ANGs, especially in RS and RS-GP 0.10% ANGs. Finally, this study demonstrates that the use of GP could be an efficient alternative to improve the biomechanical properties of ANGs with a slight impact on the biocompatibility and histological pattern. For these reasons, we hypothesize that our novel crosslinked ANGs could be a suitable alternative for future in vivo preclinical studies.
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