Proanthocyanidin surface preconditioning of dental pulp stem cell spheroids enhances dimensional stability and biomineralization in vitro

Abstract

AbstractAimLack of adequate mechanical strength and progressive shrinkage over time remain challenges in scaffold‐free microtissue‐based dental pulp regeneration. Surface collagen cross‐linking holds the promise to enhance the mechanical stability of microtissue constructs and trigger biological regulations. In this study, we proposed a novel strategy for surface preconditioning microtissues using a natural collagen cross‐linker, proanthocyanidin (PA). We evaluated its effects on cell viability, tissue integrity, and biomineralization of dental pulp stem cell (DPSCs)‐derived 3D cell spheroids.MethodologyMicrotissue and macrotissue spheroids were fabricated from DPSCs and incubated with PA solution for surface collagen cross‐linking. Microtissue viability was examined by live/dead staining and 3‐(4,5‐dimethylthiazol‐2‐yl)−2,5‐diphenyltetrazolium bromide (MTT) assay, with transverse dimension change monitored. Microtissue surface stiffness was measured by an atomic force microscope (AFM). PA‐preconditioned microtissues and macrotissues were cultured under basal or osteogenic conditions. Immunofluorescence staining of PA‐preconditioned microtissues was performed to detect dentin sialophosphoprotein (DSPP) and F‐actin expressions. PA‐preconditioned macrotissues were subjected to histological analysis, including haematoxylin–eosin (HE), alizarin red, and Masson trichrome staining. Immunohistochemistry staining was used to detect alkaline phosphatase (ALP) and dentin matrix acidic phosphoprotein 1 (DMP‐1) expressions.ResultsPA preconditioning had no adverse effects on microtissue spheroid viability and increased surface stiffness. It reduced dimensional shrinkage for over 7 days in microtissues and induced a larger transverse‐section area in the macrotissue. PA preconditioning enhanced collagen formation, mineralized nodule formation, and elevated ALP and DMP‐1 expressions in macrotissues. Additionally, PA preconditioning induced higher F‐actin and DSPP expression in microtissues, while inhibition of F‐actin activity by cytochalasin B attenuated PA‐induced dimensional change and DSPP upregulation.ConclusionPA surface preconditioning of DPSCs spheroids demonstrates excellent biocompatibility while effectively enhancing tissue structure stability and promoting biomineralization. This strategy strengthens tissue integrity in DPSC‐derived spheroids and amplifies osteogenic differentiation potential, advancing scaffold‐free tissue engineering applications in regenerative dentistry.