A Biodegradable Polymeric Matrix for the Repair of Annulus Fibrosus Defects in Intervertebral Discs.


Journal

Tissue engineering and regenerative medicine
ISSN: 2212-5469
Titre abrégé: Tissue Eng Regen Med
Pays: Korea (South)
ID NLM: 101699923

Informations de publication

Date de publication:
12 2022
Historique:
received: 09 03 2022
accepted: 19 05 2022
revised: 16 05 2022
pubmed: 12 7 2022
medline: 24 11 2022
entrez: 11 7 2022
Statut: ppublish

Résumé

Tissue defects in the annulus fibrosus (AF) due to intervertebral disc (IVD) degeneration or after nucleodiscectomy have little self-healing capacity. To prevent progressive degeneration of the IVD, the AF must be repaired. Biological closure has not yet been achieved and is a challenge for the research community. In this study, a scaffold made of absorbable poly (glycolic acid) (PGA) and hyaluronan (HA) that exhibit excellent biocompatibility and cell colonization properties was used to repair AF defects in an ovine model. A partial resection was performed in AF in L3/4 or L4/5 of 10 sheep and PGA-HA scaffolds were implanted on the defects (n = 5), while defects in the control group were left untreated (n = 5). Three months post-operation, the lumbar discs were sectioned and stained with hematoxylin and eosin and safranin-O/fast-green. Histological features including proteoglycan content, annular structure, cellular morphology, blood vessel ingrowth and tear/cleft formation were scored using a modified scoring scheme by 3 investigators and evaluated by a pathologist independently. The treated AF exhibited significantly enhanced repair tissue structure with signs of proteoglycan formation compared to the untreated group. The median scores were 4.3 for the treated and 9.8 for the untreated group. Cystic degeneration, perivascular infiltration, inflammation and necrosis were only present in the untreated group. Blood vessel ingrowth and tear/cleft formation were increased, though not significant, in the untreated group while cell morphology was comparable in both groups. PGA-HA scaffolds used for AF closure support repair tissue formation in an ovine lumbar disc defect model.

Sections du résumé

BACKGROUND
Tissue defects in the annulus fibrosus (AF) due to intervertebral disc (IVD) degeneration or after nucleodiscectomy have little self-healing capacity. To prevent progressive degeneration of the IVD, the AF must be repaired. Biological closure has not yet been achieved and is a challenge for the research community. In this study, a scaffold made of absorbable poly (glycolic acid) (PGA) and hyaluronan (HA) that exhibit excellent biocompatibility and cell colonization properties was used to repair AF defects in an ovine model.
METHODS
A partial resection was performed in AF in L3/4 or L4/5 of 10 sheep and PGA-HA scaffolds were implanted on the defects (n = 5), while defects in the control group were left untreated (n = 5). Three months post-operation, the lumbar discs were sectioned and stained with hematoxylin and eosin and safranin-O/fast-green. Histological features including proteoglycan content, annular structure, cellular morphology, blood vessel ingrowth and tear/cleft formation were scored using a modified scoring scheme by 3 investigators and evaluated by a pathologist independently.
RESULTS
The treated AF exhibited significantly enhanced repair tissue structure with signs of proteoglycan formation compared to the untreated group. The median scores were 4.3 for the treated and 9.8 for the untreated group. Cystic degeneration, perivascular infiltration, inflammation and necrosis were only present in the untreated group. Blood vessel ingrowth and tear/cleft formation were increased, though not significant, in the untreated group while cell morphology was comparable in both groups.
CONCLUSION
PGA-HA scaffolds used for AF closure support repair tissue formation in an ovine lumbar disc defect model.

Identifiants

pubmed: 35816226
doi: 10.1007/s13770-022-00466-0
pii: 10.1007/s13770-022-00466-0
pmc: PMC9679066
doi:

Substances chimiques

Hyaluronic Acid 9004-61-9
Proteoglycans 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1311-1320

Informations de copyright

© 2022. Korean Tissue Engineering and Regenerative Medicine Society.

Références

Tissue Eng Part A. 2012 Mar;18(5-6):447-58
pubmed: 21919790
Open Orthop J. 2014 Oct 17;8:346-54
pubmed: 25352927
J Tissue Eng Regen Med. 2014 Oct;8(10):811-20
pubmed: 22865642
Tissue Eng. 2005 Jan-Feb;11(1-2):1-18
pubmed: 15738657
Spine (Phila Pa 1976). 2001 Jul 15;26(14):E308-13
pubmed: 11462096
Eur Spine J. 2002 Apr;11(2):137-44
pubmed: 11956920
J Biomed Mater Res A. 2011 Dec 15;99(4):564-75
pubmed: 21936046
J Tissue Eng Regen Med. 2015 Apr;9(4):405-14
pubmed: 24227682
J Neurosurg Spine. 2012 Aug;17(2):177-83
pubmed: 22632174
Spine (Phila Pa 1976). 2003 Mar 1;28(5):446-54; discussion 453
pubmed: 12616155
Int J Mol Sci. 2017 May 12;18(5):
pubmed: 28498326
Biomaterials. 2010 Aug;31(22):5836-41
pubmed: 20430435
Biomaterials. 2013 Jul;34(23):5747-58
pubmed: 23660250
J Tissue Eng Regen Med. 2015 Oct;9(10):1120-32
pubmed: 24616324
Spine (Phila Pa 1976). 2002 Dec 1;27(23):2631-44
pubmed: 12461389
Biomater Sci. 2020 Mar 3;8(5):1216-1239
pubmed: 31957773
Dermatoendocrinol. 2012 Jul 1;4(3):253-8
pubmed: 23467280
Cartilage. 2020 Apr;11(2):192-202
pubmed: 29577749
Eur Cell Mater. 2021 Sep 24;42:166-178
pubmed: 34558056
Spine (Phila Pa 1976). 2002 Jun 15;27(12):1278-85
pubmed: 12065974
Tissue Eng. 2003 Feb;9(1):63-70
pubmed: 12625955
J Chiropr Med. 2016 Jun;15(2):155-63
pubmed: 27330520
Int J Mol Sci. 2020 Jul 10;21(14):
pubmed: 32664453
J Biomed Mater Res A. 2007 Sep 1;82(3):701-10
pubmed: 17326226
Acta Ortop Bras. 2016 Sep-Oct;24(5):262-266
pubmed: 28149193
Eur Spine J. 2009 Nov;18(11):1587-94
pubmed: 19517141
Osteoarthritis Cartilage. 2013 Dec;21(12):2039-47
pubmed: 24120397
J Orthop Surg Res. 2009 Jul 15;4:25
pubmed: 19604373
J Biomed Mater Res B Appl Biomater. 2014 May;102(4):681-92
pubmed: 24510445
Spine (Phila Pa 1976). 2004 Dec 1;29(23):2700-9
pubmed: 15564919
Tissue Eng Part A. 2008 Dec;14(12):2079-87
pubmed: 18636941
J Biomed Mater Res A. 2003 Jul 1;66(1):29-37
pubmed: 12833428
Biomaterials. 2006 Jun;27(16):3096-108
pubmed: 16460797
Eur Spine J. 2008 Jan;17(1):2-19
pubmed: 17632738
Connect Tissue Res. 2010 Apr;51(2):113-22
pubmed: 20001843
Biochim Biophys Acta. 1981 Apr 3;673(4):443-53
pubmed: 7225426
J Tissue Eng Regen Med. 2011 Apr;5(4):275-82
pubmed: 20661901
Spine (Phila Pa 1976). 2008 Jun 15;33(14):1527-32
pubmed: 18520635

Auteurs

Mohammad R Saghari Fard (MR)

TransTissue Technologies GmbH, Charitéplatz 1/Virchowweg 11, 10117, Berlin, Germany.

Jan Philipp Krueger (JP)

TransTissue Technologies GmbH, Charitéplatz 1/Virchowweg 11, 10117, Berlin, Germany.

Stefan Stich (S)

Tissue Engineering Laboratory, BIH Center for Regenerative Therapies and Department for Rheumatology and Clinical Immunology, Charité - Universitätsmedizin Berlin, Berlin, Germany.

Phil Berger (P)

TransTissue Technologies GmbH, Charitéplatz 1/Virchowweg 11, 10117, Berlin, Germany.

Anja A Kühl (AA)

Charité-Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, iPATH.Berlin, Berlin, Germany.

Michael Sittinger (M)

Tissue Engineering Laboratory, BIH Center for Regenerative Therapies and Department for Rheumatology and Clinical Immunology, Charité - Universitätsmedizin Berlin, Berlin, Germany.

Tony Hartwig (T)

Department of Back and Spinal Surgery, Vivantes Clinic Spandau, Berlin, Germany.

Michaela Endres (M)

TransTissue Technologies GmbH, Charitéplatz 1/Virchowweg 11, 10117, Berlin, Germany. michaela.endres@transtissue.com.

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Classifications MeSH