Accelerated tooth movement in Rsk2-deficient mice with impaired cementum formation
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Accelerated tooth movement in Rsk2-deficient mice with impaired cementum formation. / Nottmeier, Cita; Decker, Maximilian G; Luther, Julia; von Kroge, Simon; Kahl-Nieke, Bärbel; Amling, Michael; Schinke, Thorsten; Petersen, Julian; Koehne, Till.
in: INT J ORAL SCI, Jahrgang 12, Nr. 1, 23.12.2020, S. 35.Publikationen: SCORING: Beitrag in Fachzeitschrift/Zeitung › SCORING: Zeitschriftenaufsatz › Forschung › Begutachtung
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T1 - Accelerated tooth movement in Rsk2-deficient mice with impaired cementum formation
AU - Nottmeier, Cita
AU - Decker, Maximilian G
AU - Luther, Julia
AU - von Kroge, Simon
AU - Kahl-Nieke, Bärbel
AU - Amling, Michael
AU - Schinke, Thorsten
AU - Petersen, Julian
AU - Koehne, Till
PY - 2020/12/23
Y1 - 2020/12/23
N2 - Coffin-Lowry-Syndrome (CLS) is a X-linked mental retardation characterized by skeletal dysplasia and premature tooth loss. We and others have previously demonstrated that the ribosomal S6 kinase RSK2, mutated in CLS, is essential for bone and cementum formation; however, it remains to be established whether RSK2 plays also a role in mechanically induced bone remodeling during orthodontic tooth movement (OTM). We, therefore, performed OTM in wild-type (WT) mice and Rsk2-deficient mice using Nitinol tension springs that were fixed between the upper left molars and the incisors. The untreated contralateral molars served as internal controls. After 12 days of OTM, the jaws were removed and examined by micro-computed tomography (µCT), decalcified histology, and immunohistochemistry. Our analysis of the untreated teeth confirmed that the periodontal phenotype of Rsk2-deficient mice is characterized by alveolar bone loss and hypoplasia of root cementum. Quantification of OTM using µCT revealed that OTM was more than two-fold faster in Rsk2-deficient mice as compared to WT. We also observed that OTM caused alveolar bone loss and root resorptions in WT and Rsk2-deficient mice. However, quantification of these orthodontic side effects revealed no differences between WT and Rsk2-deficient mice. Taken together, Rsk2 loss-of-function accelerates OTM in mice without causing more side effects.
AB - Coffin-Lowry-Syndrome (CLS) is a X-linked mental retardation characterized by skeletal dysplasia and premature tooth loss. We and others have previously demonstrated that the ribosomal S6 kinase RSK2, mutated in CLS, is essential for bone and cementum formation; however, it remains to be established whether RSK2 plays also a role in mechanically induced bone remodeling during orthodontic tooth movement (OTM). We, therefore, performed OTM in wild-type (WT) mice and Rsk2-deficient mice using Nitinol tension springs that were fixed between the upper left molars and the incisors. The untreated contralateral molars served as internal controls. After 12 days of OTM, the jaws were removed and examined by micro-computed tomography (µCT), decalcified histology, and immunohistochemistry. Our analysis of the untreated teeth confirmed that the periodontal phenotype of Rsk2-deficient mice is characterized by alveolar bone loss and hypoplasia of root cementum. Quantification of OTM using µCT revealed that OTM was more than two-fold faster in Rsk2-deficient mice as compared to WT. We also observed that OTM caused alveolar bone loss and root resorptions in WT and Rsk2-deficient mice. However, quantification of these orthodontic side effects revealed no differences between WT and Rsk2-deficient mice. Taken together, Rsk2 loss-of-function accelerates OTM in mice without causing more side effects.
U2 - 10.1038/s41368-020-00102-4
DO - 10.1038/s41368-020-00102-4
M3 - SCORING: Journal article
C2 - 33353934
VL - 12
SP - 35
JO - INT J ORAL SCI
JF - INT J ORAL SCI
SN - 1674-2818
IS - 1
ER -