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口腔巨细胞病变中巨噬细胞和破骨细胞谱系的标志物。

Markers for macrophage and osteoclast lineages in giant cell lesions of the oral cavity.

作者信息

Tiffee J C, Aufdemorte T B

机构信息

Department of Oral Medicine/Pathology, University of Pittsburgh--School of Dental Medicine, PA 15261, USA.

出版信息

J Oral Maxillofac Surg. 1997 Oct;55(10):1108-12; discussion 1112-3. doi: 10.1016/s0278-2391(97)90291-3.

Abstract

PURPOSE

Giant cell lesions of the oral cavity are a well recognized entity. However, the histogenesis of these lesions is still the subject of controversy, with support for both histiocyte/macrophage and osteoclast origins being found in the literature. This study evaluated a set of peripheral giant cell lesions (PGCLs) and central giant cell lesions (CGCLs) for characteristics of both cell types to address this dilemma.

MATERIALS AND METHODS

Detection of histiocyte/macrophage characteristics was accomplished immunohistochemically by evaluating for markers specific for this cell type, namely alpha-1 -antichymotrypsin (1 -ACT) and factor XIIIa antibodies. Detection of osteoclast characteristics made use of the fact that osteoclasts possess a unique enzyme, tartrate-resistant acid phosphatase, which can be appreciated by histochemical procedures.

RESULTS

A large percentage of the multinucleated cells stained with the 1-ACT (38.08% in PGCLs and 15.84% in CGCLs), while only isolated cells stained for factor XIIIa (1.20% PGCLs, 0.99% CGCLs). Isolated stromal cells also were stained. Virtually all multinucleated cells reacted with the tartrate-resistant acid phosphatase stain (99.26% PGCLs, 98.34% CGCLs), as did a number of the mononuclear stromal cells.

CONCLUSIONS

This study supports the contention that GCLs of the oral cavity may arise from precursor cells related to the granulocyte/macrophage line, and may originate from mononuclear cells that express markers for both macrophages and osteoclasts.

摘要

目的

口腔巨细胞病变是一种公认的实体。然而,这些病变的组织发生仍然存在争议,文献中既有支持组织细胞/巨噬细胞起源的观点,也有支持破骨细胞起源的观点。本研究评估了一组外周巨细胞病变(PGCL)和中心巨细胞病变(CGCL)的两种细胞类型特征,以解决这一困境。

材料与方法

通过评估该细胞类型特异性标志物,即α-1抗糜蛋白酶(1-ACT)和因子ⅩⅢa抗体,采用免疫组织化学方法检测组织细胞/巨噬细胞特征。利用破骨细胞具有一种独特酶——抗酒石酸酸性磷酸酶这一事实,通过组织化学方法检测破骨细胞特征。

结果

大部分多核细胞用1-ACT染色(PGCL中为38.08%,CGCL中为15.84%),而仅分离的细胞用因子ⅩⅢa染色(PGCL中为1.20%,CGCL中为0.99%)。分离的基质细胞也被染色。几乎所有多核细胞对抗酒石酸酸性磷酸酶染色呈阳性反应(PGCL中为99.26%,CGCL中为98.34%),许多单核基质细胞也是如此。

结论

本研究支持如下观点,即口腔巨细胞病变可能起源于与粒细胞/巨噬细胞系相关的前体细胞,可能源自同时表达巨噬细胞和破骨细胞标志物的单核细胞。

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