Role of osteopontin in bone remodeling and orthodontic tooth movement: a review

被引:0
作者
Amarjot Singh
Gurveen Gill
Harsimrat Kaur
Mohamed Amhmed
Harpal Jakhu
机构
[1] McGill University,Faculty of Dentistry
[2] Government Dental College,Department of Endodontics
[3] Lady Davis Institute,undefined
[4] Jewish General Hospital,undefined
[5] Sandalwood Smiles,undefined
[6] Private Dental Practice,undefined
来源
Progress in Orthodontics | / 19卷
关键词
Osteopontin; Bone remodeling; Biomarkers; Root resorption; Orthodontic tooth movement;
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摘要
In this review, most of the known and postulated mechanisms of osteopontin (OPN) and its role in bone remodeling and orthodontic tooth movement are discussed based on available literature. OPN, a multifunctional protein, is considered crucial for bone remodeling, biomineralization, and periodontal remodeling during mechanical tension and stress (orthodontic tooth movement). It contributes to bone remodeling by promoting osteoclastogenesis and osteoclast activity through CD44- and αvβ3-mediated cell signaling. Further, it has a definitive role in bone remodeling by the formation of podosomes, osteoclast survival, and osteoclast motility. OPN has been shown to have a regulatory effect on hydroxyapatite crystal (HAP) growth and potently inhibits the mineralization of osteoblast cultures in a phosphate-dependent manner. Bone remodeling is vital for orthodontic tooth movement. Significant compressive and tensional forces on the periodontium induce the signaling pathways mediated by various osteogenic genes including OPN, bone sialoprotein, Osterix, and osteocalcin. The signaling pathways involved in the regulation of OPN and its effect on the periodontal tissues during orthodontic tooth movement are further discussed in this review. A limited number of studies have suggested the use of OPN as a biomarker to assess orthodontic treatment. Furthermore, the association of single nucleotide polymorphisms (SNPs) in OPN coding gene Spp1 with orthodontically induced root resorption remains largely unexplored. Accordingly, future research directions for OPN are outlined in this review.
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[1]  
Staines KA(2012)The importance of the SIBLING family of proteins on skeletal mineralisation and bone remodelling J Endocrinol 214 241-255
[2]  
MacRae VE(2000)Osteopontin Crit Rev Oral Biol Med 11 279-303
[3]  
Farquharson C(2010)Adenosine triphosphate stimulates RANKL expression through P2Y 1receptor-cyclo-oxygenase-dependent pathway in human periodontal ligament cells J Periodontal Res 45 404-411
[4]  
Sodek J(2007)Mechanical stress induces osteopontin expression in human periodontal ligament cells through rho kinase J Periodontol 78 1113-1119
[5]  
Ganss B(2008)Mechanical stress induces osteopontin via ATP/P2Y1 in periodontal cells J Dent Res 87 564-568
[6]  
McKee MD(2011)Role of connexin43 hemichannels in mechanical stress-induced ATP release in human periodontal ligament cells J Periodontal Res 46 607-615
[7]  
Luckprom P(2015)Connexin 43 and ERK regulate tension-induced signal transduction in human periodontal ligament fibroblasts J Orthop Res 33 1008-1014
[8]  
Wongkhantee S(2006)Function and regulation of osteopontin in response to mechanical stress J Bone Miner Res 21 956-964
[9]  
Yongchaitrakul T(2005)Optimal compressive force induces bone formation via increasing bone sialoprotein and prostaglandin E2 production appropriately Life Sci 77 3168-3182
[10]  
Pavasant P(1997)Expression of connexin 43 in rat mandibular bone and periodontal ligament (PDL) cells during experimental tooth movement J Dent Res 76 1357-1366