
doi: 10.1002/jcp.29994
pmid: 32740946
AbstractIntermittent parathyroid hormone (PTH) promotes periodontal repair, but the underlying mechanisms remained unclear. Recent studies found that ephrinB2‐EPHB4 forward signaling mediated the anabolic effect of PTH in bone homeostasis. Considering the similarities between cementum and bone, we aimed to examine the therapeutic effect of PTH on resorbed roots and explore the role of forward signaling in this process. In vivo experiments showed that intermittent PTH significantly accelerated the regeneration of root resorption and promoted expression of EPHB4 and ephrinB2. When the signaling was blocked, the resorption repair was also delayed. In vitro studies showed that intermittent PTH promoted the expression of EPHB4 and ephrinB2 in OCCM‐30 cells. The effects of PTH on the mineralization capacity of OCCM‐30 cells was mediated through the ephrinB2‐EPHB4 forward signaling. These results support the premise that the anabolic effects of intermittent PTH on the regeneration of root resorption is via the ephrinB2‐EPHB4 forward signaling pathway.
Dental Cementum, Male, Receptor, EphB4, Ephrin-B2, Models, Biological, Cell Line, Rats, Mice, Parathyroid Hormone, Animals, Regeneration, Cementogenesis, Rats, Wistar, Tooth Root, Tomography, X-Ray Computed, Signal Transduction
Dental Cementum, Male, Receptor, EphB4, Ephrin-B2, Models, Biological, Cell Line, Rats, Mice, Parathyroid Hormone, Animals, Regeneration, Cementogenesis, Rats, Wistar, Tooth Root, Tomography, X-Ray Computed, Signal Transduction
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