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Compressive Force-Induced Autophagy in Periodontal Ligament Cells Downregulates Osteoclastogenesis During Tooth Movement.
Journal of Periodontology 2019 May 12
BACKGROUND: Autophagy has recently emerged as a protective mechanism in response to compressive force and an important process in maintenance of bone homeostasis. It appears to be involved in the degradation of osteoclasts, osteoblasts and osteocytes. The aim of this study was to investigate the role of compressive force-induced autophagy in periodontal ligament (PDL) cells in regulating osteoclastogenesis of orthodontic tooth movement (OTM).
METHODS: An OTM model and compressive force on PDL cells were employed to investigate the expression of autophagy markers in vivo and in vitro, respectively. Autophagosomes and autolysosomes were observed in PDL cells by Transmission electron microscope (TEM) and Autophagy LC3 Double-Labelling. 3-methyladenine (3-MA) and rapamycin were respectively used to inhibit and promote autophagy, and the effect of autophagy on osteoclastogenesis was explored via microcomputed tomography (micro-CT), haematoxylin and eosin (HE) staining, histochemistry of titrate-resistant acid phosphatase (TRAP) and real-time PCR (RT-PCR) in vivo. RANKL/OPG was investigated by RT-PCR and ELISA in vitro.
RESULTS: Orthodontic force-induced autophagy was prominent on the pressured side of PDL tissues. Administration of 3-MA downregulated bone density and upregulated osteoclasts, while rapamycin had reverse results in OTM. The autophagy activity increased initially then decreased in PDL cells during compressive force application and responded to light force. In PDL cells, administration of 3-MA upregulated while rapamycin downregulated the RANKL/OPG ratio.
CONCLUSIONS: Autophagy in PDL cells is activated with compressive force and could modulate OTM by negatively regulates osteoclastogenesis and keep bone homeostasis via RANKL/OPG signalling. This article is protected by copyright. All rights reserved.
METHODS: An OTM model and compressive force on PDL cells were employed to investigate the expression of autophagy markers in vivo and in vitro, respectively. Autophagosomes and autolysosomes were observed in PDL cells by Transmission electron microscope (TEM) and Autophagy LC3 Double-Labelling. 3-methyladenine (3-MA) and rapamycin were respectively used to inhibit and promote autophagy, and the effect of autophagy on osteoclastogenesis was explored via microcomputed tomography (micro-CT), haematoxylin and eosin (HE) staining, histochemistry of titrate-resistant acid phosphatase (TRAP) and real-time PCR (RT-PCR) in vivo. RANKL/OPG was investigated by RT-PCR and ELISA in vitro.
RESULTS: Orthodontic force-induced autophagy was prominent on the pressured side of PDL tissues. Administration of 3-MA downregulated bone density and upregulated osteoclasts, while rapamycin had reverse results in OTM. The autophagy activity increased initially then decreased in PDL cells during compressive force application and responded to light force. In PDL cells, administration of 3-MA upregulated while rapamycin downregulated the RANKL/OPG ratio.
CONCLUSIONS: Autophagy in PDL cells is activated with compressive force and could modulate OTM by negatively regulates osteoclastogenesis and keep bone homeostasis via RANKL/OPG signalling. This article is protected by copyright. All rights reserved.
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