The Role of Cyclic AMP, Calcium, and Prostaglandins in the Induction of Osteoclastic Bone Resorption Associated with Experimental Tooth Movement

1983 ◽  
Vol 62 (8) ◽  
pp. 877-881 ◽  
Author(s):  
K. Yamasaki
2018 ◽  
Vol 9 ◽  
Author(s):  
Brendan F. Boyce ◽  
Jinbo Li ◽  
Lianping Xing ◽  
Zhenqiang Yao

2014 ◽  
Vol 73 (4) ◽  
pp. 112-113
Author(s):  
Tsutomu Matsumoto ◽  
Tadahiro Iimura ◽  
Kenji Ogura ◽  
Keiji Moriyama ◽  
Akira Yamaguchi

2013 ◽  
Vol 92 (4) ◽  
pp. 340-345 ◽  
Author(s):  
T. Matsumoto ◽  
T. Iimura ◽  
K. Ogura ◽  
K. Moriyama ◽  
A. Yamaguchi

Author(s):  
A. Hirashita ◽  
Y. Nakamura ◽  
E. Okumura ◽  
Y. Kuwabara

Biological functions of Ca in mitochondrial granules have been reported by a number of investigators. It is said that mitochondrial granules of chondrocytes, osteoblasts and osteocytes in rat epiphyseal growth plate with regard to bone calcification and these granules of osteoclasts at bone-resorbing site play an important role of Ca-transport. However, these results were reported about the first stage of calcification in rat epiphyseal growth plate, so that the changes of bone tissues in adult rats seem to be not always the same.The purpose of this work is, by electron probe X-ray microanalysis method, to do the elemental analysis in mitochondrial granules of osteoblasts, osteocytes and osteoclasts incident to experimental tooth movement in adult rats, and to compare them with these analysis in control groups.


2006 ◽  
Vol 24 (5) ◽  
pp. 368-372 ◽  
Author(s):  
Takuma Matsubara ◽  
Akira Myoui ◽  
Fumiyo Ikeda ◽  
Kenji Hata ◽  
Hideki Yoshikawa ◽  
...  

Author(s):  
Niklas Ullrich ◽  
Agnes Schröder ◽  
Maria Bauer ◽  
Gerrit Spanier ◽  
Jonathan Jantsch ◽  
...  

Summary Background In orthodontic tooth movement (OTM), pseudo-inflammatory processes occur that are similar to those of nicotine-induced periodontitis. Previous studies have shown that nicotine accelerates OTM, but induces periodontal bone loss and dental root resorption via synergistically increased osteoclastogenesis. This study aimed to investigate the role of hypoxia-inducible factor 1 alpha (HIF-1α) in nicotine-induced osteoclastogenesis during OTM. Materials/Methods Male Fischer-344 rats were treated with l-Nicotine (1.89 mg/kg/day s.c., N = 10) or NaCl solution (N = 10). After a week of premedication, a NiTi spring was inserted to mesialize the first upper left molar. The extent of dental root resorption, osteoclastogenesis, and HIF-1α protein expression was determined by (immuno)histology, as well as bone volume (BV/TV) and trabecular thickness (TbTh) using µCT. Receptor activator of nuclear factor of activated B-cells ligand (RANK-L), osteoprotegerin (OPG), and HIF-1α expression were examined at the protein level in periodontal ligament fibroblasts (PDLF) exposed to pressure, nicotine and/or hypoxia, as well as PDLF-induced osteoclastogenesis in co-culture experiments with osteoclast progenitor cells. Results Nicotine favoured dental root resorptions and osteoclastogenesis during OTM, while BV/TV and TbTh were only influenced by force. This nicotine-induced increase does not appear to be mediated by HIF-1α, since HIF-1α was stabilized by force application and hypoxia, but not by nicotine. The in vitro data showed that the hypoxia-induced increase in RANK-L/OPG expression ratio and PDLF-mediated osteoclastogenesis was less pronounced than the nicotine-induced increase. Conclusions Study results indicate that the nicotine-induced increase in osteoclastogenesis and periodontal bone resorption during OTM may not be mediated by hypoxic effects or HIF-1α stabilization in the context of nicotine-induced vasoconstriction, but rather by an alternative mechanism.


1995 ◽  
Vol 207 (1) ◽  
pp. 280-287 ◽  
Author(s):  
T.J. Hall ◽  
M. Schaeublin ◽  
H. Jeker ◽  
K. Fuller ◽  
T.J. Chambers

2021 ◽  
Vol 22 (13) ◽  
pp. 6934
Author(s):  
Anh Chu ◽  
Ralph A. Zirngibl ◽  
Morris F. Manolson

This review focuses on one of the 16 proteins composing the V-ATPase complex responsible for resorbing bone: the a3 subunit. The rationale for focusing on this biomolecule is that mutations in this one protein account for over 50% of osteopetrosis cases, highlighting its critical role in bone physiology. Despite its essential role in bone remodeling and its involvement in bone diseases, little is known about the way in which this subunit is targeted and regulated within osteoclasts. To this end, this review is broadened to include the three other mammalian paralogues (a1, a2 and a4) and the two yeast orthologs (Vph1p and Stv1p). By examining the literature on all of the paralogues/orthologs of the V-ATPase a subunit, we hope to provide insight into the molecular mechanisms and future research directions specific to a3. This review starts with an overview on bone, highlighting the role of V-ATPases in osteoclastic bone resorption. We then cover V-ATPases in other location/functions, highlighting the roles which the four mammalian a subunit paralogues might play in differential targeting and/or regulation. We review the ways in which the energy of ATP hydrolysis is converted into proton translocation, and go in depth into the diverse role of the a subunit, not only in proton translocation but also in lipid binding, cell signaling and human diseases. Finally, the therapeutic implication of targeting a3 specifically for bone diseases and cancer is discussed, with concluding remarks on future directions.


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