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破骨细胞的起源:对胚胎期大鼠骨骼中巨噬细胞与破骨细胞的免疫组织化学研究

The origin of osteoclasts: an immunohistochemical study on macrophages and osteoclasts in embryonic rat bone.

作者信息

Sminia T, Dijkstra C D

出版信息

Calcif Tissue Int. 1986 Oct;39(4):263-6. doi: 10.1007/BF02555216.

Abstract

The origin of osteoclasts was studied in embryonic rat bone primordia using a set of monoclonal antibodies (ED1, ED2, and ED3) that exclusively recognize monocytes and macrophage. ED1 recognizes monocytes and macrophages. Mononuclear phagocytes which were ED1 positive were found in the perichondrium/periosteum of developing bone. These cells started to infiltrate the primordia when the cartilage became hypertrophic. During bone formation, multinucleated ED1-positive cells with the morphological characteristics of osteoclasts were found in the developing bone marrow cavity and against the bone collar. The present findings support the notion that osteoclasts arise by fusion of mononuclear phagocytes derived from blood monocytes.

摘要

利用一组专门识别单核细胞和巨噬细胞的单克隆抗体(ED1、ED2和ED3),对胚胎期大鼠骨原基中破骨细胞的起源进行了研究。ED1识别单核细胞和巨噬细胞。在发育中骨骼的软骨膜/骨膜中发现了ED1阳性的单核吞噬细胞。当软骨肥大时,这些细胞开始浸润原基。在骨形成过程中,在发育中的骨髓腔和骨环处发现了具有破骨细胞形态特征的多核ED1阳性细胞。目前的研究结果支持破骨细胞由血液单核细胞衍生的单核吞噬细胞融合产生这一观点。

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