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血小板抗原和纤维蛋白原在破骨细胞上的定位。

Localization of platelet antigens and fibrinogen on osteoclasts.

作者信息

Athanasou N A, Quinn J, Heryet A, McGee J O

机构信息

University of Oxford, Nuffield Department of Pathology, John Radcliffe Hospital, Headington, UK.

出版信息

J Cell Sci. 1988 Jan;89 ( Pt 1):115-22. doi: 10.1242/jcs.89.1.115.

Abstract

The antigenic phenotype of the human osteoclast, which is known to be derived from a circulating mononuclear precursor cell of haemopoietic origin, is controversial. Recent studies have shown that macrophage as well as megakaryocyte/platelet antigens are expressed by osteoclasts. In this study, we have sought to define, by immunohistochemistry, the nature and possible function of platelet antigens expressed by human osteoclasts in foetal and adult bone specimens. Monoclonal antibodies to platelet glycoprotein IIIa (gpIIIa) and CD9 antibodies stained osteoclasts in all bone specimens examined. Fibrinogen was also localized to the osteoclast membrane in foetal bone imprints. In addition, we found that CD9 and gpIIIa antibodies reacted weakly with monocytes in buffy coat smears. Antibodies to factor 8 and glycoproteins Ib and IIb/IIIa did not react with osteoclasts. These results show that osteoclasts, monocytes, macrophages, megakaryocytes and platelets possess common antigens and that fibrinogen is present on the surface of osteoclasts. By analogy with platelets, CD9 and gpIIIa may play a role in fibrinogen binding by osteoclasts. Possible mechanisms by which platelet antigens and fibrinogen binding could affect osteoclast function are proposed.

摘要

已知人类破骨细胞源自造血来源的循环单核前体细胞,但其抗原表型存在争议。最近的研究表明,破骨细胞表达巨噬细胞以及巨核细胞/血小板抗原。在本研究中,我们试图通过免疫组织化学来确定胎儿和成人骨标本中人类破骨细胞所表达的血小板抗原的性质和可能的功能。针对血小板糖蛋白IIIa(gpIIIa)的单克隆抗体和CD9抗体在所有检测的骨标本中均能对破骨细胞进行染色。在胎儿骨印片中,纤维蛋白原也定位于破骨细胞膜上。此外,我们发现CD9和gpIIIa抗体与血沉棕黄层涂片中的单核细胞反应较弱。针对因子8以及糖蛋白Ib和IIb/IIIa的抗体与破骨细胞无反应。这些结果表明,破骨细胞、单核细胞、巨噬细胞、巨核细胞和血小板具有共同抗原,并且纤维蛋白原存在于破骨细胞表面。与血小板类似,CD9和gpIIIa可能在破骨细胞结合纤维蛋白原的过程中发挥作用。本文提出了血小板抗原和纤维蛋白原结合可能影响破骨细胞功能的潜在机制。

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