Biofabrication of an ovine intervertebral disc model by combining a polycaprolactone frame with a bioprinted alginate hydrogel

The intervertebral disc (IVD) primarily comprises an outer ring of collagen fibers (annulus fibrosus, AF), which encases a soft, gelatinous core (nucleus pulposus, NP). Existing<i>in vitro</i>models have failed to integrate these two tissues effectively or accurately replicate their intricate organization. By combining two biofabrication techniques, we developed a novel 3D<i>in vitro</i>model that closely mimics the organization of an ovine IVD. Our approach employs a polycaprolactone (PCL) frame produced via melt electrowriting to recreate the multilamellar architecture of the AF. Ovine primary cells, encapsulated in a photocrosslinkable alginate hydrogel, were precisely extruded within the multilamellar structure, thereby mimicking the native shape and size of an ovine disc. The bioink containing the NP cells was deposited at the center of the construct, while the bioink with the AF cells was strategically layered in between the lamellae of the PCL frame. Photocrosslinking was optimized to match the native stiffness of the disc. The constructs were maintained in culture for 28 d, during which we thoroughly assessed reproducibility, stability, and cell viability and phenotype. The results unequivocally demonstrated that the PCL frame effectively guided the alignment and proliferation of AF cells, while the alginate hydrogel preserved NP cell phenotype. This model successfully replicates the organization of the IVD, providing a promising platform for advancing our understanding of disc biology and driving the development of novel therapeutic strategies.

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Publication Details

Journal
Biofabrication
Published
2025-09-26
DOI
https://doi.org/10.1088/1758-5090/ae0c3e
Citations
2
Primary Topic
Spine and Intervertebral Disc Pathology
Type
article
Field-Weighted Citation Impact
2.94
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article

Biofabrication of an ovine intervertebral disc model by combining a polycaprolactone frame with a bioprinted alginate hydrogel

Catherine Le Visage, Michael G. Monaghan, Vianney Delplace, Diego Contreras et al.
2 citations
Biofabrication
Spine and Intervertebral Disc Pathology
2.94
article

Biofabrication of an ovine intervertebral disc model by combining a polycaprolactone frame with a bioprinted alginate hydrogel

Catherine Le Visage, Michael G. Monaghan, Vianney Delplace, Diego Contreras, Boris Halgand, Jérôme Guicheux, Marion Fusellier, Mansoor Chaaban, Joëlle Véziers, François Loll, Johann Clouet, Emmaëlle Carrot, Clara Schiex
article en
2 citations

Abstract

The intervertebral disc (IVD) primarily comprises an outer ring of collagen fibers (annulus fibrosus, AF), which encases a soft, gelatinous core (nucleus pulposus, NP). Existing<i>in vitro</i>models have failed to integrate these two tissues effectively or accurately replicate their intricate organization. By combining two biofabrication techniques, we developed a novel 3D<i>in vitro</i>model that closely mimics the organization of an ovine IVD. Our approach employs a polycaprolactone (PCL) frame produced via melt electrowriting to recreate the multilamellar architecture of the AF. Ovine primary cells, encapsulated in a photocrosslinkable alginate hydrogel, were precisely extruded within the multilamellar structure, thereby mimicking the native shape and size of an ovine disc. The bioink containing the NP cells was deposited at the center of the construct, while the bioink with the AF cells was strategically layered in between the lamellae of the PCL frame. Photocrosslinking was optimized to match the native stiffness of the disc. The constructs were maintained in culture for 28 d, during which we thoroughly assessed reproducibility, stability, and cell viability and phenotype. The results unequivocally demonstrated that the PCL frame effectively guided the alignment and proliferation of AF cells, while the alginate hydrogel preserved NP cell phenotype. This model successfully replicates the organization of the IVD, providing a promising platform for advancing our understanding of disc biology and driving the development of novel therapeutic strategies.

BiofabricationVol. 17(4)
Inserm (FR), Trinity College Dublin (IE), Nantes Université (FR)
Openalex Percentile: Top 8%
Spine and Intervertebral Disc Pathology
2.94
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