Suppr超能文献

破骨细胞分化抗原

Osteoclast differentiation antigen.

作者信息

Kukita T, Kukita A

机构信息

Second Department of Oral Anatomy, Faculty of Dentistry, Kyushu University, Fukuoka, Japan.

出版信息

Histol Histopathol. 1996 Jul;11(3):821-30.

PMID:8839769
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.

摘要

破骨细胞是执行骨吸收的主要细胞。这些多核巨细胞起源于造血干细胞。到目前为止,破骨细胞的分化途径已得到充分研究,这些骨吸收细胞的细胞谱系被认为与单核细胞/巨噬细胞密切相关但并不完全相同。由于用于评估破骨细胞分化的体外培养系统的发展,已经阐明多种细胞因子参与破骨细胞的分化。然而,破骨细胞分化的分子机制仍存在模糊之处。阐明分子机制的一种方法是找到参与破骨细胞分化过程的独特抗原分子。在这篇综述文章中,我们介绍了有关破骨细胞分化的此类免疫学研究。我们还提及了我们最近建立的一组识别大鼠破骨细胞的单克隆抗体。其中一种单克隆抗体识别在破骨细胞谱系细胞上表达而不在单核细胞/巨噬细胞上表达的细胞表面抗原(Kat1抗原)。使用这种单克隆抗体对细胞表面抗原进行交联表明,Kat1抗原是参与调节降钙素受体亲和力且也参与调节骨吸收的独特细胞表面分子。在这篇综述文章中,我们概述了为理解破骨细胞的分化和激活而应阐明的当前问题。我们进一步强调免疫学方法在解决这些当前目标问题方面的实用性。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验