Distinguish fatty acids impact survival, differentiation and cellular function of periodontal ligament fibroblasts

GND
1161568298
ORCID
0000-0001-9347-0172
Zugehörigkeit
Department of Orthodontics, University Hospital Jena
Symmank, Judit;
GND
1299972985
Zugehörigkeit
Department of Orthodontics, University Hospital Jena
Chorus, Martin;
GND
1238384862
Zugehörigkeit
Department of Orthodontics, University Hospital Jena
Appel, Sophie;
Zugehörigkeit
Department of Orthodontics, University Hospital RWTH Aachen, Aachen, Germany
Marciniak, Jana;
Zugehörigkeit
Department of Orthodontics, University Hospital RWTH Aachen, Aachen, Germany
Knaup, Isabel;
Zugehörigkeit
Department of Orthodontics, University Hospital RWTH Aachen, Aachen, Germany
Bastian, Asisa;
GND
1042166463
Zugehörigkeit
Department of Orthodontics, University Hospital Jena
Hennig, Christoph-Ludwig;
GND
1043069240
Zugehörigkeit
Section of Geriodontics, Department of Conservative Dentistry and Periodontics, University Hospital Jena
Döding, Annika;
GND
1177276429
Zugehörigkeit
Section of Geriodontics, Department of Conservative Dentistry and Periodontics, University Hospital Jena,
Schulze-Späte, Ulrike;
GND
131607596
Zugehörigkeit
Department of Orthodontics, University Hospital Jena
Jacobs, Collin;
Zugehörigkeit
Department of Orthodontics, University Hospital RWTH Aachen, Aachen, Germany
Wolf, Michael

Alveolar bone (AB) remodeling is necessary for the adaption to mechanical stimuli occurring during mastication and orthodontic tooth movement (OTM). Thereby, bone degradation and assembly are strongly regulated processes that can be altered in obese patients. Further, increased fatty acids (FA) serum levels affect bone remodeling cells and we, therefore, investigated whether they also influence the function of periodontal ligament fibroblast (PdLF). PdLF are a major cell type regulating the differentiation and function of osteoblasts and osteoclasts localized in the AB. We stimulated human PdLF (HPdLF) in vitro with palmitic (PA) or oleic acid (OA) and analyzed their metabolic activity, growth, survival and expression of osteogenic markers and calcium deposits. Our results emphasize that PA increased cell death of HPdLF, whereas OA induced their osteoblastic differentiation. Moreover, quantitative expression analysis of OPG and RANKL revealed altered levels in mechanically stimulated PA-treated HPdLF. Furthermore, osteoclasts stimulated with culture medium of mechanical stressed FA-treated HPdLF revealed significant changes in cell differentiation upon FA-treatment. For the first time, our results highlight a potential role of specific FA in the function of HPdLF-modulated AB remodeling and help to elucidate the complex interplay of bone metabolism, mechanical stimulation and obesity-induced alterations.

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