Fibronectin-gelatin nanofilm coating improves dental pulp stem cell survival and differentiation in odontogenesis-mimicking organotypic 3D bilayered constructs

Healthcare professionals, researchers, patients and their families affected by rare diseases face many difficulties during diagnosis. A targeted diagnostic tool, using high-throughput sequencing (NGS) technologies, known as GenoDENT, used to unravel molecular diagnosis behind rare diseases with oral and dental manifestations, enabled the identification of more than 15% of variants of unknown significance (Class III - VUS), beside a high 70%-80% diagnostic rate in the analyzed patients' cohort. VUS make diagnosis more difficult because they prevent precise correlation between genotype and phenotype. To overcome this issue, we are developing 3D <i>in vitro</i> models mimicking odontogenesis. Our first 3D models, made of odontoblast-like and ameloblast-like cells, were effective when using murine cells. They were stable over time and showed a good distinction between both used cell types. However, the formation of 3D models from human cells was less efficient, so we decided to couple the 3D model formation technique with the cell-accumulation method to produce stable 3D constructs. This process consists in covering the cells with a biomimetic artificial matrix made of fibronectin (FN) and gelatin (G). We found that FN/G coating improved viability of human dental pulp stem cells (hDPSC) in thick constructs and promoted odontoblast differentiation of hDPSC. In peripheral ameloblast-like cells, ameloblast-associated proteins such as amelogenin were detected in close contact with the odontoblast-like core. We believe that our model can be further modified to introduce patient-specific variations through gene-editing techniques like CRISPR/Cas9, for further development of new diagnostic tools applied to rare oro-dental diseases.

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Publication Details

Journal
Frontiers in Dental Medicine
Published
2026-02-23
DOI
https://doi.org/10.3389/fdmed.2026.1763201
Primary Topic
Bone and Dental Protein Studies
Type
article
Field-Weighted Citation Impact
0.00

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article

Fibronectin-gelatin nanofilm coating improves dental pulp stem cell survival and differentiation in odontogenesis-mimicking organotypic 3D bilayered constructs

Alexandra Jimenez-Armijo, Marzena Kawczynski, Youri Arntz, Varvara Gribova et al.
Frontiers in Dental Medicine
Bone and Dental Protein Studies
article

Fibronectin-gelatin nanofilm coating improves dental pulp stem cell survival and differentiation in odontogenesis-mimicking organotypic 3D bilayered constructs

Alexandra Jimenez-Armijo, Marzena Kawczynski, Youri Arntz, Varvara Gribova, Fadi Jerbaka, Gaétan Caravello, Isaac Maximiliano Bugueno, Eve Suss
article en

Abstract

Healthcare professionals, researchers, patients and their families affected by rare diseases face many difficulties during diagnosis. A targeted diagnostic tool, using high-throughput sequencing (NGS) technologies, known as GenoDENT, used to unravel molecular diagnosis behind rare diseases with oral and dental manifestations, enabled the identification of more than 15% of variants of unknown significance (Class III - VUS), beside a high 70%-80% diagnostic rate in the analyzed patients' cohort. VUS make diagnosis more difficult because they prevent precise correlation between genotype and phenotype. To overcome this issue, we are developing 3D <i>in vitro</i> models mimicking odontogenesis. Our first 3D models, made of odontoblast-like and ameloblast-like cells, were effective when using murine cells. They were stable over time and showed a good distinction between both used cell types. However, the formation of 3D models from human cells was less efficient, so we decided to couple the 3D model formation technique with the cell-accumulation method to produce stable 3D constructs. This process consists in covering the cells with a biomimetic artificial matrix made of fibronectin (FN) and gelatin (G). We found that FN/G coating improved viability of human dental pulp stem cells (hDPSC) in thick constructs and promoted odontoblast differentiation of hDPSC. In peripheral ameloblast-like cells, ameloblast-associated proteins such as amelogenin were detected in close contact with the odontoblast-like core. We believe that our model can be further modified to introduce patient-specific variations through gene-editing techniques like CRISPR/Cas9, for further development of new diagnostic tools applied to rare oro-dental diseases.

Frontiers in Dental MedicineVol. 7
Université d'Orléans (FR), University of Zurich (CH), Institut de génétique et de biologie moléculaire et cellulaire (FR), Hôpitaux Universitaires de Strasbourg (FR), Université de Strasbourg (FR)
Agence Nationale de la Recherche
Openalex Percentile: Top 49%
Bone and Dental Protein Studies
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