Level C· Early human research exploring benefitsProspective StudyEurope PMCOpen access

Wnt7B enhances the osteogenic differentiation of lipopolysaccharide-stimulated human periodontal ligament stem cells and inhibits the M1 polarization of macrophages by binding FZD4

Yang H., Zhang Y., Zhang L., Tan X., Zhi M., Wang C.

Prospective Study on Ligament Injury, published in Mol Med Rep (2024) — summary generated from the PubMed abstract.

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Level C· Early human research exploring benefitsEvidence level of this study

Early human evidence such as case series or small samples is exploring possible benefits.

  • Level A · Stronger Clinical Evidence
  • Level B · Emerging clinical evidence with positive signals
  • Level C · Early human research exploring benefits
  • Level D · Scientific groundwork from lab and animal studies
  • Emerging · Emerging topic under active research
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This page is generated from the PubMed record. The Thai description is an automated summary of bibliographic fields and the abstract, not a full translation, and is not medical advice.

Study type
Prospective Study
Journal
Mol Med Rep (2024)
Reported sample size
—
Source database
Europe PMC
PMID
39301638
PMCID
PMC11413851
DOI
10.3892/mmr.2024.13327

Abstract (original English)

Periodontitis, a common oral disease characterized by the progressive infiltration of bacteria, is a leading cause of adult tooth loss. Periodontal stem cells (PDLSCs) possess good self‑renewal and multi‑potential differentiation abilities to maintain the integrity of periodontal support structure and repair defects. The present study aimed to analyze the roles of Wnt7B and frizzled4 (FZD4) in the osteogenic differentiation and macrophage polarization during periodontitis using an in vitro cell model. First, Wnt7B expression in the periodontitis‑affected gingival tissue of patients and lipopolysaccharide (LPS)‑stimulated PDLSCs was assessed using the GSE23586 dataset and western blot analysis, respectively. In Wnt7B‑overexpressing PDLSCs exposed to LPS, the capacity of osteogenic differentiation was evaluated by detecting alkaline phosphatase activity, the level of Alizarin Red S staining and the expression of genes related to osteogenic differentiation. Subsequently, conditioned medium from PDLSCs overexpressing Wnt7B was used for M0 macrophage culture. The expression of CD86 and INOS was examined using immunofluorescence staining and western blot analysis. In addition, reverse transcription‑quantitative PCR was employed to examine the expression of TNF‑α, IL‑6 and IL‑1β in macrophages. The binding between Wnt7B and FZD4 was estimated using co‑immunoprecipitation. In addition,

What this study does not prove

  • • This study does not prove SVF is an approved treatment or a replacement for standard care.

Evidence level

Early human evidence such as case series or small samples is exploring possible benefits.

How we grade evidence
Cells, CulturedMacrophagesStem CellsPeriodontal LigamentHumansPeriodontitisLipopolysaccharidesCell DifferentiationProtein BindingOsteogenesis

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