Injectable hydrogel induces regeneration of naturally degenerate human intervertebral discs in a loaded organ culture model.

Human Organ Culture Injectable Biomaterial Intervertebral disc

Journal

Acta biomaterialia
ISSN: 1878-7568
Titre abrégé: Acta Biomater
Pays: England
ID NLM: 101233144

Informations de publication

Date de publication:
29 Dec 2023
Historique:
received: 02 10 2023
revised: 30 11 2023
accepted: 22 12 2023
medline: 2 1 2024
pubmed: 2 1 2024
entrez: 31 12 2023
Statut: aheadofprint

Résumé

Low back pain resulting from disc degeneration is a leading cause of disability worldwide. However, to date few therapies target the cause and fail to repair the intervertebral disc (IVD). This study investigates the ability of an injectable hydrogel (NPgel), to inhibit catabolic protein expression and promote matrix expression in human nucleus pulposus (NP) cells within a tissue explant culture model isolated from degenerate discs. Furthermore, the injection capacity of NPgel into naturally degenerate whole human discs, effects on mechanical function, and resistance to extrusion during loading were investigated. Finally, the induction of potential regenerative effects in a physiologically loaded human organ culture system was investigated following injection of NPgel with or without bone marrow progenitor cells. Injection of NPgel into naturally degenerate human IVDs increased disc height and Young's modulus, and was retained during extrusion testing. Injection into cadaveric discs followed by culture under physiological loading increased MRI signal intensity, restored natural biomechanical properties and showed evidence of increased anabolism and decreased catabolism with tissue integration observed. These results provide essential proof of concept data supporting the use of NPgel as an injectable therapy for disc regeneration. STATEMENT OF SIGNIFICANCE: Low back pain resulting from disc degeneration is a leading cause of disability worldwide. However, to date few therapies target the cause and fail to repair the intervertebral disc. This study investigated the potential regenerative properties of an injectable hydrogel system (NPgel) within human tissue samples. To mimic the human in vivo conditions and the unique IVD niche, a dynamically loaded intact human disc culture system was utilised. NPgel improved the biomechanical properties, increased MRI intensity and decreased degree of degeneration. Furthermore, NPgel induced matrix production and decreased catabolic factors by the native cells of the disc. This manuscript provides evidence for the potential use of NPgel as a regenerative biomaterial for intervertebral disc degeneration.

Identifiants

pubmed: 38160855
pii: S1742-7061(23)00754-7
doi: 10.1016/j.actbio.2023.12.041
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2023. Published by Elsevier Ltd.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: Christine Le Maitre reports financial support was provided by Versus Arthritis. Christine Le Maitre reports financial support was provided by UKRI Medical Research Council. Lisbeth Haglund reports financial support was provided by Canadian Institutes of Health Research. Christine Le Maitre reports a relationship with Orthoson Ltd that includes: consulting or advisory. Christine Le Maitre & Christopher Sammon have patents #Composite hydrogels GB2493933B, US2014219973A, EP2747797A licensed to Orthoson.

Auteurs

Hosni Cherif (H)

Department of Surgery, McGill University, Montreal, QC H3G 1A4, Canada.

Li Li (L)

Department of Surgery, McGill University, Montreal, QC H3G 1A4, Canada.

Joseph Snuggs (J)

Oncology and Metabolism Department, Medical School, & INSIGNEO Institute, University of Sheffield, Sheffield, UK; Biomolecular Sciences Research Centre, Sheffield Hallam University, Sheffield, UK.

Xuan Li (X)

Department of Mechanical Engineering, McGill University, Montreal, QC H3A 0C3, Canada.

Christopher Sammon (C)

Materials and Engineering Research Institute, Sheffield Hallam University, Sheffield, UK.

Jianyu Li (J)

Department of Surgery, McGill University, Montreal, QC H3G 1A4, Canada; Department of Mechanical Engineering, McGill University, Montreal, QC H3A 0C3, Canada; Department of Biomedical Engineering, McGill University, Montreal, QC H3A 2B4, Canada.

Lorne Beckman (L)

Department of Surgery, McGill University, Montreal, QC H3G 1A4, Canada.

Lisbet Haglund (L)

Department of Surgery, McGill University, Montreal, QC H3G 1A4, Canada; Shriners Hospital for Children, Montreal, QC H4A 0A9, Canada.

Christine L Le Maitre (CLL)

Oncology and Metabolism Department, Medical School, & INSIGNEO Institute, University of Sheffield, Sheffield, UK; Biomolecular Sciences Research Centre, Sheffield Hallam University, Sheffield, UK.

Classifications MeSH