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Role of c-Fos in orthodontic tooth movement: an in vivo study using transgenic mice.
Decker, Maximilian G; Nottmeier, Cita; Luther, Julia; Baranowsky, Anke; Kahl-Nieke, Bärbel; Amling, Michael; Schinke, Thorsten; David, Jean-Pierre; Koehne, Till.
Afiliación
  • Decker MG; Department of Orthodontics, University Medical Center Hamburg-Eppendorf, Martinistr. 52, 20246, Hamburg, Germany.
  • Nottmeier C; Department of Orthodontics, University Medical Center Hamburg-Eppendorf, Martinistr. 52, 20246, Hamburg, Germany.
  • Luther J; Institute of Osteology and Biomechanics, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
  • Baranowsky A; Institute of Osteology and Biomechanics, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
  • Kahl-Nieke B; Department of Orthodontics, University Medical Center Hamburg-Eppendorf, Martinistr. 52, 20246, Hamburg, Germany.
  • Amling M; Institute of Osteology and Biomechanics, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
  • Schinke T; Institute of Osteology and Biomechanics, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
  • David JP; Institute of Osteology and Biomechanics, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
  • Koehne T; Department of Orthodontics, University Medical Center Hamburg-Eppendorf, Martinistr. 52, 20246, Hamburg, Germany. tkoehne@uke.de.
Clin Oral Investig ; 25(2): 593-601, 2021 Feb.
Article en En | MEDLINE | ID: mdl-32803442
ABSTRACT

OBJECTIVES:

The transcription factor c-Fos controls the differentiation of osteoclasts and is expressed in periodontal ligament cells after mechanical stimulation in vitro. However, it is unclear how c-Fos regulates orthodontic tooth movement (OTM) in vivo. The aim of this study was therefore to analyse OTM in transgenic mice with overexpression of c-Fos. MATERIALS AND

METHODS:

We employed c-Fos transgenic mice (c-Fos tg) and wild-type littermates (WT) in a model of OTM induced by Nitinol tension springs that were bonded between the left first maxillary molars and the upper incisors. The unstimulated contralateral side served as an internal control. Mice were analysed by contact radiography, micro-computed tomography, decalcified histology and histochemistry.

RESULTS:

Our analysis of the unstimulated side revealed that alveolar bone and root morphology were similar between c-Fos tg and control mice. However, we observed more osteoclasts in the alveolar bone of c-Fos tg mice as tartrate-resistant acid phosphatase (TRAP)-positive cells were increased by 40%. After 12 days of OTM, c-Fos tg mice exhibited 62% increased tooth movement as compared with WT mice. Despite the faster tooth movement, c-Fos tg and WT mice displayed the same amount of root resorption. Importantly, we did not observe orthodontically induced tissue necrosis (i.e. hyalinization) in c-Fos tg mice, while this was a common finding in WT mice.

CONCLUSION:

Overexpression of c-Fos accelerates tooth movement without causing more root resorption. CLINICAL RELEVANCE Accelerated tooth movement must not result in more root resorption as higher tissue turnover may decrease the amount of mechanically induced tissue necrosis.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Resorción Radicular / Técnicas de Movimiento Dental Tipo de estudio: Prognostic_studies Límite: Animals Idioma: En Revista: Clin Oral Investig Asunto de la revista: ODONTOLOGIA Año: 2021 Tipo del documento: Article País de afiliación: Alemania

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Resorción Radicular / Técnicas de Movimiento Dental Tipo de estudio: Prognostic_studies Límite: Animals Idioma: En Revista: Clin Oral Investig Asunto de la revista: ODONTOLOGIA Año: 2021 Tipo del documento: Article País de afiliación: Alemania