Localization of osteopontin and osterix in periodontal tissue during orthodontic tooth movement in rats

被引:24
作者
Kim, Ji-Youn [2 ]
Kim, Byung-In [2 ]
Jue, Seong-Suk [1 ]
Park, Jae Hyun [1 ,3 ]
Shin, Je-Won [1 ]
机构
[1] Kyung Hee Univ, Grad Sch Dent, Seoul, South Korea
[2] Kyung Hee Univ, Dept Oral Anat & Dev Biol, Div Dent, Grad Sch, Seoul, South Korea
[3] AT Still Univ, Postgrad Orthodont Program, Arizona Sch Dent & Oral Hlth, Mesa, AZ USA
关键词
Orthodontic tooth movement; Periodontal tissue; OPN; Osterix; MESSENGER-RNA; OSTEOCALCIN EXPRESSION; BONE; DIFFERENTIATION; PROLIFERATION; OSTEOCLASTS; PROTEINS;
D O I
10.2319/030911-173.1
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Objective: To evaluate the localization of osteopontin (OPN) and osterix in periodontal tissue during experimental tooth movement with heavy force in rats. Materials and Methods: Nickel-titanium closed-coil springs were used to create a 100 g mesial force to the maxillary first molars. On days 3, 7, 10, and 14 after force application, histological changes in periodontium were examined by immunohistochemistry using proliferating cell nuclear antigen (PCNA), OPN, and osterix. Results: PCNA-positive cells were found close to the alveolar bone and cementum on both sides. OPN-positive cells were observed along the cementing line of the cementum and bone on both sides and also were visible along with newly formed fibers in the periodontal ligament on the tension side. Osterix-positive cells were strongly detected on the surface of the alveolar bone and cementum on both sides. Conclusions: During tooth movement, periodontal remodeling occurs on both sides. These results indicate that OPN and osterix may play an important role of differentiation and osteoblasts and cementoblasts matrix formation during periodontal tissue remodeling. (Angle Orthod. 2012;82:107-114.)
引用
收藏
页码:107 / 114
页数:8
相关论文
共 24 条
[1]   Osterix is a key target for mechanical signals in human thoracic ligament flavum cells [J].
Fan, Dongwei ;
Chen, Zhongqiang ;
Wang, Dan ;
Guo, Zhaoqing ;
Qiang, Qi ;
Shang, Yongfeng .
JOURNAL OF CELLULAR PHYSIOLOGY, 2007, 211 (03) :577-584
[2]   Function and regulation of osteopontin in response to mechanical stress [J].
Fujihara, Shinji ;
Yokozeki, Masahiko ;
Oba, Yasuo ;
Higashibata, Yuji ;
Nomura, Shintaro ;
Moriyama, Keiji .
JOURNAL OF BONE AND MINERAL RESEARCH, 2006, 21 (06) :956-964
[3]   Force magnitude and duration effects on amount of tooth movement and root resorption in the rat molar [J].
Gonzales, Carmen ;
Hotokezaka, Hitoshi ;
Yoshimatsu, Masako ;
Yozgatian, Joseph H. ;
Darendeliler, M. Ali ;
Yoshida, Noriaki .
ANGLE ORTHODONTIST, 2008, 78 (03) :502-509
[4]  
HIRAKAWA K, 1994, J BONE MINER RES, V9, P1551
[5]   Localization of Runx2, Osterix, and Osteopontin in Tooth Root Formation in Rat Molars [J].
Hirata, Azumi ;
Sugahara, Toshio ;
Nakamura, Hiroaki .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 2009, 57 (04) :397-403
[6]   The effect of fluoride administration on rat serum osteocalcin expression during orthodontic movement [J].
Kebsch, Mark ;
Wilkinson, Margaret ;
Petocz, Peter ;
Darendeliler, M. Ali .
AMERICAN JOURNAL OF ORTHODONTICS AND DENTOFACIAL ORTHOPEDICS, 2007, 131 (04) :515-524
[7]   SENSITIVITY OF OSTEOCYTES TO BIOMECHANICAL STRESS IN-VITRO [J].
KLEINNULEND, J ;
VANDERPLAS, A ;
SEMEINS, CM ;
AJUBI, NE ;
FRANGOS, JA ;
NIJWEIDE, PJ ;
BURGER, EH .
FASEB JOURNAL, 1995, 9 (05) :441-445
[8]  
Krishnan V., 2006, AM J ORTHOD DENTOFAC, V129, p469., DOI [10.1016/j.ajodo.2005.10.007, DOI 10.1016/J.AJODO.2005.10.007]
[9]   Expression of osteopontin mRNA in odontoclasts revealed by in situ hybridization during experimental tooth movement in mice [J].
Kuroda, S ;
Balam, TA ;
Sakai, Y ;
Tamamura, N ;
Takano-Yamamoto, T .
JOURNAL OF BONE AND MINERAL METABOLISM, 2005, 23 (02) :110-113
[10]  
Lee JY, 2006, MOL CELLS, V22, P182