良、恶性口腔病变中含有因子XIII亚单位a的细胞特征。

The Histochemical Journal Pub Date : 1995-06-01
M Toida, Y Okumura, K K Swe Win, N Oka, T Takami, R Adány
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引用次数: 0

摘要

本研究研究了含因子XIII亚单位a (FXIII a)的细胞在人颊黏膜良恶性病变中的分布规律和特征。通过双免疫荧光染色技术研究了来自四个刺激性纤维瘤和三个鳞状细胞癌的组织,其中FXIII A的检测与CD14(识别单核细胞/巨噬细胞分化标记抗原),Mac 387(与巨噬细胞的特殊亚群反应),抗hla - dr, Ki-M7(标记吞噬巨噬细胞)或Ki-67(显示与细胞增殖相关的核抗原)单克隆抗体的反应相结合。良、恶性口腔病变结缔组织间质细胞中均检测到fxiiia。这些FXIII A-反应细胞(FXIII A+细胞)的数量在肿瘤组织中显著增加,特别是在肿瘤细胞群周围。分散在纤维瘤组织中的FXIII A+细胞呈纺锤形,而在肿瘤间质中,以大的星状细胞为主,血管周围同样标记有圆形细胞。FXIII A+细胞被CD14和Ki-M7标记在纤维瘤和肿瘤颊粘膜;然而,它们与Ki-67没有任何反应。积聚在肿瘤基质中的FXIII A+细胞也对HLA-DR产生反应。这些结果表明,在良性和恶性口腔病变中,fxiiia都包含在组织巨噬细胞亚群中,这代表了单核细胞衍生(CD14+)和吞噬(Ki-M7+)细胞群。FXIII A+细胞在肿瘤基质中的积累被认为是循环血液直接迁移的结果。(摘要删节250字)
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Characterization of cells containing factor XIII subunit a in benign and malignant buccal lesions.

In the present study, the distribution pattern and characteristics of cells containing Factor XIII subunit a (FXIII A) have been studied in benign and malignant lesions of human buccal mucosa. Tissues from four irritation fibromas and three squamous cell carcinomas were studied by means of double immunofluorescent staining techniques in which the detection of FXIII A was combined with a reaction with CD14 (recognizing a monocyte/macrophage differentiation marker antigen), Mac 387 (reacting with a special subset of macrophages), anti-HLA-DR, Ki-M7 (labelling phagocytosing macrophages) or Ki-67 (visualizing a nuclear antigen associated with cell proliferation) monoclonal antibodies. FXIII A was detected in cells of the connective tissue stroma in both benign and malignant buccal lesions. The number of these FXIII A-reactive cells (FXIII A+ cells) increased considerably in the tumour tissues, in particular in those surrounding tumour cell clusters. FXIII A+ cells scattered in the fibromatous tissues were spindle-shaped, whereas in the tumour stroma, large stellate cells predominated, and round cells were likewise labelled around blood vessels. FXIII A+ cells were labelled with CD14 and Ki-M7 in both fibromatous and tumoural buccal mucosa; however, they failed to show any reaction with Ki-67. FXIII A+ cells accumulated in the tumour stroma reacted for HLA-DR as well. These results indicate that in both the benign and malignant buccal lesions FXIII A is contained in a subpopulation of tissue macrophages, which represents a monocyte-derived (CD14+) and phagocytosing (Ki-M7+) cell population. The accumulation of the FXIII A+ cells in the tumour stroma is believed to be a result of direct migration from the circulating blood.(ABSTRACT TRUNCATED AT 250 WORDS)

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