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颌骨巨细胞肉芽肿中的多核细胞是破骨细胞。

The multinucleate cells in giant cell granulomas of the jaw are osteoclasts.

作者信息

Flanagan A M, Nui B, Tinkler S M, Horton M A, Williams D M, Chambers T J

机构信息

Department of Histopathology, St George's Hospital Medical School, London, United Kingdom.

出版信息

Cancer. 1988 Sep 15;62(6):1139-45. doi: 10.1002/1097-0142(19880915)62:6<1139::aid-cncr2820620617>3.0.co;2-8.

Abstract

The giant cell granuloma of jaw is a well-vascularised lesion comprising a mononuclear cell infiltrate with a large number of giant cells. It has been suggested that the lesion is reparative in nature, rather than neoplastic, and that the giant cells are phagocytes accumulating in chronic reparative granulation tissue. However, the nature of the multinucleate giant cells never has been established. One possibility is that the constituent giant cells are osteoclasts. The authors assessed expression by the giant cells of several osteoclast-specific characteristics: excavation of bone; motility inhibition by calcitonin (CT); and binding of osteoclast specific monoclonal antibodies. Two tumors were disaggregated and incubated on slices of cortical bone in the presence and absence of CT. Both tumors were found to excavate bone, a function unique to osteoclasts. The giant cells also were responsive to CT, resulting in cytoplasmic quiescence and inhibition of bone resorption. Two osteoclast-specific monoclonal antibodies bound all the giant cells in one central and six peripheral tumors examined immunohistochemically. These results provide strong evidence for the osteoclastic nature of the giant cells. The presence of alkaline phosphatase-positive cells forming woven bone in giant cell granulomas suggests that osteoblasts are present in the lesion. As cells of osteoblastic lineage are known to regulate osteoclastic function, it may be that osteoblasts account for the characteristic infiltration of osteoclasts into giant cell granulomas of jaws, either as part of a reparative response by reactive osteoblasts or as an infiltrate induced by osteoblasts of aberrant function, as suggested for giant cell tumors of bone.

摘要

颌骨巨细胞肉芽肿是一种血管丰富的病变,由单核细胞浸润和大量巨细胞组成。有人认为该病变本质上是修复性的,而非肿瘤性的,且巨细胞是积聚在慢性修复性肉芽组织中的吞噬细胞。然而,多核巨细胞的性质尚未确定。一种可能性是组成巨细胞为破骨细胞。作者评估了巨细胞的几种破骨细胞特异性特征的表达:骨吸收;降钙素(CT)对其运动的抑制作用;以及破骨细胞特异性单克隆抗体的结合情况。将两个肿瘤解离,并在有无CT的情况下在皮质骨切片上孵育。发现两个肿瘤均能进行骨吸收,这是破骨细胞特有的功能。巨细胞也对CT有反应,导致细胞质静止并抑制骨吸收。两种破骨细胞特异性单克隆抗体在免疫组织化学检查中与一个中央肿瘤和六个外周肿瘤中的所有巨细胞结合。这些结果为巨细胞的破骨细胞性质提供了有力证据。在巨细胞肉芽肿中存在形成编织骨的碱性磷酸酶阳性细胞,提示病变中存在成骨细胞。由于已知成骨细胞系细胞可调节破骨细胞功能,可能是成骨细胞导致破骨细胞特征性地浸润到颌骨巨细胞肉芽肿中,要么是作为反应性成骨细胞修复反应的一部分,要么是如骨巨细胞瘤中所提示的那样,由功能异常的成骨细胞诱导的浸润。

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