Evidence map›Paper›PMID 42308664›Full record

ArticleInternational dental journal2026

κ-Carrageenan-Based Hydrogels Support Viability and Odontogenic Differentiation of Stem Cells From the Apical Papilla.

Muneera A Alajlan, Rhodanne Nicole A Lambarte, Terrence S Sumague, Abdurahman A Niazy

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Article in International dental journal, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

4 authors.

Muneera A AlajlanDepartment of Restorative Dental Sciences, College of Dentistry, King Saud University, Riyadh, Kingdom of Saudi Arabia.
Rhodanne Nicole A LambarteMolecular and Cell Biology Laboratory, Prince Naif bin AbdulAziz Health Research Center, King Saud University Medical City, Riyadh, Kingdom of Saudi Arabia.
Terrence S SumagueMolecular and Cell Biology Laboratory, Prince Naif bin AbdulAziz Health Research Center, King Saud University Medical City, Riyadh, Kingdom of Saudi Arabia.
Abdurahman A NiazyMolecular and Cell Biology Laboratory, Prince Naif bin AbdulAziz Health Research Center, King Saud University Medical City, Riyadh, Kingdom of Saudi Arabia; Department of Oral Medicine and Diagnostic Sciences, College of Dentistry, King Saud University, Riyadh, Kingdom of Saudi Arabia. Electronic address: aaniazy@ksu.edu.sa.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

INTRODUCTION AND

aimsImmature teeth with pulp necrosis remain challenging because conventional root canal treatment does not restore pulp-dentin vitality. Hydrogel scaffolds for regenerative endodontics should support stem cell viability and provide a microenvironment favourable for dentin-pulp regeneration. This study evaluated κ-Carrageenan (κC)-based hydrogels, with and without gelatin, as scaffolds for stem cells from the apical papilla (SCAP), and examined how formulation-dependent properties influenced SCAP viability and odontogenic differentiation.

methodsHydrogels were prepared as 1% gelatin, 1.5% κC, 2.5% κC, 1.5% κC+gelatin (κCG) and 2.5% κCG, with cells cultured without hydrogel as a control. Physicochemical characterisation included scanning electron microscopy, Fourier-transform infrared spectroscopy, rheology, degradation and swelling at days 1, 3, 7 and 14. SCAP were isolated and characterised using flow cytometry. Cell viability, metabolic activity, spreading, migration, alkaline phosphatase activity, Alizarin Red S staining and qPCR of differentiation-related markers were also assessed.

resultsThe hydrogels showed formulation-dependent microstructure, degradation, swelling and viscoelastic properties. κC-containing formulations behaved as viscoelastic solids, and 2.5% κCG exhibited the highest storage modulus and lowest Tan (δ). SCAP remained predominantly viable in all groups. Gelatin-containing hydrogels improved long-term cytocompatibility and greater cell spreading compared to lower-concentration κC alone. Migration was comparable across groups. During differentiation, κC-containing formulations showed higher alkaline phosphatase activity and mineral deposition, with increased late-stage mineralisation observed in 2.5% κCG. Gene expression analysis indicated early upregulation of RUNX2 and BSP and increased late-stage expression of OPN, OCN, DMP1 and DSPP, with a more evident maturation-associated response in 2.5% κCG.

conclusionκC-based hydrogels supported SCAP viability and promoted odontogenic differentiation in vitro. Gelatin incorporation improved late-stage mineralisation and odontogenic marker expression, with 2.5% κCG demonstrating the most favourable overall response. CLINICAL RELEVANCE: κC-gelatin hydrogels may serve as promising scaffold candidates for dentin-pulp regenerative strategies by supporting SCAP survival and odontogenic maturation within a tunable hydrogel microenvironment.

Indexed as

CarrageenanCell DifferentiationDental PapillaHydrogelsOdontogenesisStem CellsAlkaline PhosphataseCells, CulturedCell SurvivalDentin SialophosphoproteinExtracellular Matrix ProteinsFlow CytometryGelatinHumansMicroscopy, Electron, ScanningOsteocalcinAlkaline PhosphataseCarrageenanDentin SialophosphoproteinDMP1 protein, humanExtracellular Matrix ProteinsGelatinHydrogelsOsteocalcinOsteopontinPhosphoproteinsSialoglycoproteinsDentin-pulp regenerationGelatin hydrogelOdontogenic differentiationRegenerative endodonticsStem cells from apical papillaκ-Carrageenan

Identifiers

PMID42308664
PMCPMC13311808

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