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针对骨巨细胞瘤(巨细胞骨肿瘤)的单克隆抗体:破骨细胞特异性细胞抗原的定义

Monoclonal antibodies to osteoclastomas (giant cell bone tumors): definition of osteoclast-specific cellular antigens.

作者信息

Horton M A, Lewis D, McNulty K, Pringle J A, Chambers T J

出版信息

Cancer Res. 1985 Nov;45(11 Pt 2):5663-9.

PMID:4053038
Abstract

The cellular origin of the osteoclast, the major agent of bone resorption, remains controversial despite the demonstration that osteoclasts form by fusion of mononuclear cells that are ultimately derived from a bone marrow stem cell. One view is that they are the terminally differentiated progeny of mononuclear phagocytic cells. However, we have previously provided evidence, from functional and phenotypic studies of rodent and human osteoclasts, that raises the possibility that osteoclasts form a separate cell lineage from conventional hemopoietic cells and macrophages in particular. In an attempt to elucidate this question, we have used monoclonal antibody techniques to examine the relationship between osteoclasts and other bone marrow-derived cells. By using osteoclasts from osteoclastomas (giant cell tumors of bone) for immunizations, we have produced 11 mouse hybridomas secreting monoclonal antibodies reacting with osteoclasts in normal human fetal bone and a variety of neoplastic and non-neoplastic bone lesions. Eight antibodies in 4 reactivity sets have been shown to recognize membrane antigens, whereas a further 3 react with cytoplasmic determinants. In 7 there is no cross-reactivity with macrophages in a wide range of tissues, thus effectively differentiating between these two cell types. These antibodies will prove useful for the identification of osteoclasts in tissues and in the separation of their circulating precursors, thus allowing an experimental approach to be made to many of the outstanding questions regarding the developmental pathobiology of the osteoclast.

摘要

破骨细胞是骨吸收的主要作用因子,尽管已经证实破骨细胞是由最终来源于骨髓干细胞的单核细胞融合形成的,但破骨细胞的细胞起源仍存在争议。一种观点认为它们是单核吞噬细胞的终末分化后代。然而,我们之前通过对啮齿动物和人类破骨细胞的功能和表型研究提供了证据,这增加了破骨细胞形成一个独立于传统造血细胞,特别是巨噬细胞的细胞谱系的可能性。为了阐明这个问题,我们使用单克隆抗体技术来研究破骨细胞与其他骨髓来源细胞之间的关系。通过用骨巨细胞瘤(骨的巨细胞瘤)中的破骨细胞进行免疫,我们产生了11个小鼠杂交瘤,它们分泌的单克隆抗体与正常人类胎儿骨以及各种肿瘤性和非肿瘤性骨病变中的破骨细胞发生反应。已证明4个反应组中的8种抗体识别膜抗原,而另外3种与细胞质决定簇反应。在7种抗体中,与广泛组织中的巨噬细胞没有交叉反应,从而有效地区分了这两种细胞类型。这些抗体将被证明可用于在组织中鉴定破骨细胞以及分离其循环前体,从而为解决许多关于破骨细胞发育病理生物学的突出问题提供一种实验方法。

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