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Enhancing Dental Pulp Stem Cell Proliferation and Odontogenic Differentiation with Protein Phosphatase 1-Disrupting Peptide: An In Vitro Study.
Kobrock, Anna; Matos, Bárbara; Patrício, Daniela; Grenho, Liliana; Howl, John; Fardilha, Margarida; Gomes, Pedro S.
Affiliation
  • Kobrock A; Signal Transduction Laboratory, Institute of Biomedicine-iBiMED, University of Aveiro, 3810-193 Aveiro, Portugal.
  • Matos B; BoneLab-Laboratory for Bone Metabolism and Regeneration, Faculty of Dental Medicine, University of Porto, 4200-393 Porto, Portugal.
  • Patrício D; LAQV/REQUIMTE, Faculty of Dental Medicine, University of Porto, 4200-393 Porto, Portugal.
  • Grenho L; Signal Transduction Laboratory, Institute of Biomedicine-iBiMED, University of Aveiro, 3810-193 Aveiro, Portugal.
  • Howl J; Signal Transduction Laboratory, Institute of Biomedicine-iBiMED, University of Aveiro, 3810-193 Aveiro, Portugal.
  • Fardilha M; BoneLab-Laboratory for Bone Metabolism and Regeneration, Faculty of Dental Medicine, University of Porto, 4200-393 Porto, Portugal.
  • Gomes PS; LAQV/REQUIMTE, Faculty of Dental Medicine, University of Porto, 4200-393 Porto, Portugal.
Cells ; 13(13)2024 Jul 03.
Article in En | MEDLINE | ID: mdl-38994993
ABSTRACT
The reparative and regenerative capabilities of dental pulp stem cells (DPSCs) are crucial for responding to pulp injuries, with protein phosphatase 1 (PP1) playing a significant role in regulating cellular functions pertinent to tissue healing. Accordingly, this study aimed to explore the effects of a novel cell-penetrating peptide Modified Sperm Stop 1-MSS1, that disrupts PP1, on the proliferation and odontogenic differentiation of DPSCs. Employing MSS1 as a bioportide, DPSCs were cultured and characterized for metabolic activity, cell proliferation, and cell morphology alongside the odontogenic differentiation through gene expression and alkaline phosphatase (ALP) activity analysis. MSS1 exposure induced early DPSC proliferation, upregulated genes related to odontogenic differentiation, and increased ALP activity. Markers associated with early differentiation events were induced at early culture time points and those associated with matrix mineralization were upregulated at mid-culture stages. This investigation is the first to document the potential of a PP1-disrupting bioportide in modulating DPSC functionality, suggesting a promising avenue for enhancing dental tissue regeneration and repair.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Stem Cells / Cell Differentiation / Dental Pulp / Cell Proliferation / Protein Phosphatase 1 / Odontogenesis Limits: Humans Language: En Journal: Cells Year: 2024 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Stem Cells / Cell Differentiation / Dental Pulp / Cell Proliferation / Protein Phosphatase 1 / Odontogenesis Limits: Humans Language: En Journal: Cells Year: 2024 Document type: Article Affiliation country: