Literature DB >> 8839769

Osteoclast differentiation antigen.

T Kukita1, A Kukita.   

Abstract

Osteoclasts are the primary cells which perform bone resorption. The origin of these multinucleated giant cells is the haematopoietic stem cells. The differentiation pathway of the osteoclasts has so far been well studied and the cell-lineage of these bone resorbing cells is considered to be close but not identical to the monocytes/macrophages. Owing to the development of in vitro culture systems for evaluating osteoclast differentiation, it has been elucidated that various cytokines are involved in the differentiation of the osteoclasts. However, there is still ambiguity concerning the molecular mechanism of the differentiation of the osteoclasts. One approach for clarifying the molecular mechanism is to find unique antigen molecules involved in the process of osteoclast differentiation. In this review article, we introduce such immunological studies concerning osteoclast differentiation. We also refer to our recent establishment of a panel of monoclonal antibodies recognizing rat osteoclasts. One of the monoclonal antibodies recognizes cell surface antigen (Kat1-antigen) expressed on cells in osteoclast-lineage and not on monocytes/macrophages. Cross-linking of the cell surface antigen using this monoclonal antibody showed that the Kat1-antigen is the unique cell surface molecule involved in the regulation of the affinity of the calcitonin receptor and also involved in the modulation of bone resorption. In this review article, we overview, the current issues which should be elucidated for understanding the differentiation and activation of the osteoclasts. We further emphasize the utility of the immunological approach for solving these current target issues.

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Year:  1996        PMID: 8839769

Source DB:  PubMed          Journal:  Histol Histopathol        ISSN: 0213-3911            Impact factor:   2.303


  3 in total

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Journal:  J Biol Chem       Date:  2015-04-02       Impact factor: 5.157

2.  Prednisone prevents particle induced bone loss in the calvaria mouse model.

Authors:  Michael M Schündeln; Jakob Höppner; Felix L Meyer; Wiebke Schmuck; Max D Kauther; Gero Hilken; Bodo Levkau; Martina Rauner; Corinna Grasemann
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3.  Adenosine blocks aminopterin-induced suppression of osteoclast differentiation.

Authors:  Junpei Teramachi; Akiko Kukita; Pengfei Qu; Naohisa Wada; Yin-Ji Li; Seiji Nakamura; Toshio Kukita
Journal:  J Bone Miner Metab       Date:  2012-11-01       Impact factor: 2.626

  3 in total

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