Osteoclast recruitment to sites of compression in orthodontic tooth movement.

Although it is widely acknowledged that osteoclasts are formed by the fusion of mononuclear cells of hematopoietic origin, it has been extremely difficult to understand how they originate after appliance activation. The purpose of this study was to quantify osteoclast recruitment at compression sites as a function of time following orthodontic force application. Appliances were placed in 96 rats. At day 0, the animals were randomized to either appliance activation or sham activation followed by the injection of 5-bromo-2'-deoxyuridine (BrdU). Thus, BrdU was incorporated into the nuclei of cells in S-phase, including hematopoietic stem cells. Groups of 10 to 13 rats were killed at 1, 3, 5, and 7 days after activation/sham, and the tissue samples were prepared. The numbers of BrdU-labeled cells positively stained with tartrate-resistant acid phosphatase (TRAP) were measured in the periodontium. A significant number of BrdU-positive preosteoclasts was observed in the periodontal ligament (PDL) and bone surface at day 3. The number of osteoclastic cells in the bone marrow also peaked at day 3; however, the highest percentage of cells in this location was observed at day 1. These data suggest that osteoclasts in the PDL originate by the fusion of recently recruited preosteoclasts from the marrow instead of from local PDL cells. Furthermore, the alveolar bone marrow plays a role in the formation of osteoclasts during orthodontic tooth movement.

[1]  G. King,et al.  Effect of appliance reactivation after decay of initial activation on osteoclasts, tooth movement, and root resorption. , 1999, The Angle orthodontist.

[2]  K. Moriyama,et al.  Expression of cathepsin K mRNA during experimental tooth movement in rat as revealed by in situ hybridization. , 2000, Archives of oral biology.

[3]  H. Birkedal‐Hansen Biological mechanisms of tooth movement and craniofacial adaptation , 1993 .

[4]  G. King,et al.  Serum and alveolar bone phosphatase changes reflect bone turnover during orthodontic tooth movement. , 1993, American journal of orthodontics and dentofacial orthopedics : official publication of the American Association of Orthodontists, its constituent societies, and the American Board of Orthodontics.

[5]  M. Hong,et al.  Interleukin 1 regulates the expression of osteopontin mRNA by osteoblasts , 1990, Molecular and Cellular Endocrinology.

[6]  E H Burger,et al.  Cells of bone: proliferation, differentiation, and hormonal regulation. , 1986, Physiological reviews.

[7]  M. S. Burstone,et al.  HISTOCHEMICAL DEMONSTRATION OF ACID PHOSPHATASE ACTIVITY IN OSTEOCLASTS , 1959, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

[8]  J. Loutit,et al.  Osteoclasts derived from haematopoietic stem cells , 1980, Nature.

[9]  G. King,et al.  Later orthodontic appliance reactivation stimulates immediate appearance of osteoclasts and linear tooth movement. , 1998, American journal of orthodontics and dentofacial orthopedics : official publication of the American Association of Orthodontists, its constituent societies, and the American Board of Orthodontics.

[10]  P Rygh,et al.  Elimination of hyalinized periodontal tissues associated with orthodontic tooth movement. , 1974, Scandinavian journal of dental research.

[11]  G. King,et al.  Histomorphometric and biochemical study of osteoclasts at orthodontic compression sites in the rat during indomethacin inhibition. , 1997, Archives of oral biology.

[12]  S. Palle,et al.  Pre-osteoblastic Proliferation Assessed with BrdU in Undecalcified, Epon-embedded Adult Rat Trabecular Bone , 1997, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

[13]  D. Eyre,et al.  Molecular basis and clinical application of biological markers of bone turnover. , 1996, Endocrine reviews.

[14]  G. King,et al.  Effect of orthodontic appliance reactivation during the period of peak expansion in the osteoclast population , 1998, The Anatomical record.

[15]  K. Rajewsky,et al.  Dividing cells in bone marrow and spleen incorporate bromodeoxyuridine with high efficiency , 1991, European journal of immunology.

[16]  G. King,et al.  Measuring dental drift and orthodontic tooth movement in response to various initial forces in adult rats. , 1991, American journal of orthodontics and dentofacial orthopedics : official publication of the American Association of Orthodontists, its constituent societies, and the American Board of Orthodontics.

[17]  K Reitan,et al.  Some factors determining the evaluation of forces in orthodontics , 1957 .

[18]  Y. Shibasaki,et al.  Distributional Changes of Osteoclasts and Pre-osteoclastic Cells in Periodontal Tissues during Experimental Tooth Movement as Revealed by Quantitative Immunohistochemistry of H+-ATPase , 1997, Journal of dental research.

[19]  E. Herbst,et al.  Regeneration of blood-forming organs after autologous leukocyte transfusion in lethally irradiated dogs. I. Distribution and cellularity of the bone marrow in normal dogs. , 1975, Blood.

[20]  Marty Jj,et al.  The effect of cobalt-60 irradiation on bone marrow cellularity and alveolar osteoclasts. , 1995 .

[21]  P. Sinclair,et al.  The local use of vitamin D to increase the rate of orthodontic tooth movement. , 1988, American Journal of Orthodontics and Dentofacial Orthopedics.

[22]  D. G. Walker Control of bone resorption by hematopoietic tissue. The induction and reversal of congenital osteopetrosis in mice through use of bone marrow and splenic transplants , 1975, The Journal of experimental medicine.

[23]  M. H. Chen,et al.  Osteoclast activation and recruitment after application of orthodontic force. , 1999, American journal of orthodontics and dentofacial orthopedics : official publication of the American Association of Orthodontists, its constituent societies, and the American Board of Orthodontics.

[24]  A. Wetterwald,et al.  Detection of transcripts for the receptor for macrophage colony-stimulating factor, c-fms, in murine osteoclasts. , 1992, Proceedings of the National Academy of Sciences of the United States of America.

[25]  T. Cate,et al.  Oral histology: Development, structure, and function , 1980 .

[26]  A. deFazio,et al.  Immunohistochemical detection of proliferating cells in vivo. , 1987, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

[27]  E. Kvam,et al.  Comparative behavior of human and animal tissue during experimental tooth movement. , 2009, The Angle orthodontist.

[28]  N. Udagawa,et al.  Cells of Bone , 2002 .

[29]  T. Yamashiro,et al.  The Effect of Local Application of 1,25-Dihydroxycholecalciferol on Osteoclast Numbers in Orthodontically Treated Rats , 1992, Journal of dental research.

[30]  N. Athanasou,et al.  Use of monoclonal antibodies to recognise osteoclasts in routinely processed bone biopsy specimens. , 1991, Journal of clinical pathology.

[31]  M. Iwamoto,et al.  Effects of Continuous Infusion of PTH on Experimental Tooth Movement in Rats , 1999, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

[32]  T. Wronski,et al.  Histomorphometric study of alveolar bone turnover in orthodontic tooth movement. , 1991, Bone.

[33]  O. Laerum,et al.  Cytometry and time-dependent variations in peripheral blood and bone marrow cells: a literature review and relevance to the chronotherapy of cancer. , 1991, Chronobiology international.

[34]  P. J. Anderson,et al.  HISTOCHEMICAL METHODS FOR ACID PHOSPHATASE USING HEXAZONIUM PARAROSANILIN AS COUPLER , 1962 .

[35]  J. Ferguson,et al.  Correlation of tooth movement with variable forces in the cat. , 1973, The Angle orthodontist.

[36]  V. Everts,et al.  Loss of connective tissue attachment in the marginal periodontium of the mouse following blockage of eruption. , 1982, Journal of periodontal research.

[37]  R. Baron,et al.  Cellular kinetics of the bone remodeling sequence in the rat , 1982, The Anatomical record.

[38]  S. Herring,et al.  Differential cell replication within the periosteum of the pig mandibular ramus. , 1996, Acta anatomica.

[39]  R. Maronpot,et al.  Variations in the Histologic Distribution of Rat Bone Marrow Cells with Respect to Age and Anatomic Site , 1985, Toxicologic pathology.

[40]  M. Drezner,et al.  Bone histomorphometry: Standardization of nomenclature, symbols, and units: Report of the asbmr histomorphometry nomenclature committee , 1987, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

[41]  E H Hixon,et al.  On force and tooth movement. , 1970, American journal of orthodontics.

[42]  Y. Muguruma,et al.  Isolation and characterization of murine clonogenic osteoclast progenitors by cell surface phenotype analysis. , 1998, Blood.

[43]  S. Clark,et al.  Macrophage colony-stimulating factor stimulates survival and chemotactic behavior in isolated osteoclasts , 1993, The Journal of experimental medicine.

[44]  W. Nothdurft,et al.  The development of radiation late effects to the bone marrow after single and chronic exposure. , 1986, International journal of radiation biology and related studies in physics, chemistry, and medicine.

[45]  J. Bitran Bone marrow, structure and function , 1983 .

[46]  W. Jee,et al.  Cell kinetics of orthodontically-stimulated and non-stimulated periodontal ligament in the rat. , 1974, Archives of oral biology.

[47]  J. Ward,et al.  Persistence of 5-bromo-2'-deoxyuridine in tissues of rats after exposure in early life. , 1991, Toxicology.