GDF15 Promotes the Osteogenic Cell Fate of Periodontal Ligament Fibroblasts, thus Affecting Their Mechanobiological Response

GND
1324032073
Zugehörigkeit
Department of Orthodontics, University Hospital Jena, Leutragraben 3, 07743 Jena, Germany
Lösch, Lukas;
GND
1252370725
Zugehörigkeit
Department of Orthodontics, University Hospital Jena, Leutragraben 3, 07743 Jena, Germany
Stemmler, Albert;
GND
1324033002
Zugehörigkeit
Department of Orthodontics, University Hospital Jena, Leutragraben 3, 07743 Jena, Germany
Fischer, Adrian;
GND
1252372868
Zugehörigkeit
Department of Orthodontics, University Hospital Jena, Leutragraben 3, 07743 Jena, Germany
Steinmetz, Julia;
GND
1272890015
Zugehörigkeit
Department of Orthodontics, University Hospital Jena, Leutragraben 3, 07743 Jena, Germany
Schuldt, Lisa;
GND
1042166463
Zugehörigkeit
Department of Orthodontics, University Hospital Jena, Leutragraben 3, 07743 Jena, Germany
Hennig, Christoph-Ludwig;
GND
1161568298
ORCID
0000-0001-9347-0172
Zugehörigkeit
Department of Orthodontics, University Hospital Jena, Leutragraben 3, 07743 Jena, Germany
Symmank, Judit;
GND
131607596
Zugehörigkeit
Department of Orthodontics, University Hospital Jena, Leutragraben 3, 07743 Jena, Germany
Jacobs, Collin

Periodontal ligament fibroblasts (PdLFs) exert important functions in oral tissue and bone remodeling following mechanical forces, which are specifically applied during orthodontic tooth movement (OTM). Located between the teeth and the alveolar bone, mechanical stress activates the mechanomodulatory functions of PdLFs including regulating local inflammation and activating further bone-remodeling cells. Previous studies suggested growth differentiation factor 15 (GDF15) as an important pro-inflammatory regulator during the PdLF mechanoresponse. GDF15 exerts its effects through both intracrine signaling and receptor binding, possibly even in an autocrine manner. The extent to which PdLFs are susceptible to extracellular GDF15 has not yet been investigated. Thus, our study aims to examine the influence of GDF15 exposure on the cellular properties of PdLFs and their mechanoresponse, which seems particularly relevant regarding disease- and aging-associated elevated GDF15 serum levels. Therefore, in addition to investigating potential GDF15 receptors, we analyzed its impact on the proliferation, survival, senescence, and differentiation of human PdLFs, demonstrating a pro-osteogenic effect upon long-term stimulation. Furthermore, we observed altered force-related inflammation and impaired osteoclast differentiation. Overall, our data suggest a major impact of extracellular GDF15 on PdLF differentiation and their mechanoresponse.

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