含因子XIII亚单位a的细胞在人表皮细胞强烈纤维化灶周围的积累。

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

摘要

根据临床和生化结果,推测因子XIII亚单位a (FXIII a)在纤维化过程中起重要作用。以纤维化组织形成不同阶段的Epulis样品为模型系统,研究结缔组织生成过程中FXIII a的定位和组织分布。同时测定含有FXIII A的细胞(FXIII A+细胞)的标记特性。在双免疫荧光标记系统中,FXIII A定位于单核细胞源性(CD-14+)、活化性(HLA-DR+)和吞噬性(Ki-M7+)组织巨噬细胞中,这些巨噬细胞广泛均匀分布于肉芽组织中,但一旦病灶出现,就开始在纤维化灶周围聚集。在较长的纤维化过程中,FXIII A+巨噬细胞数量不断减少,形态外观由星状变为纺锤状。这些细胞细胞核未被Ki-67单克隆抗体标记;这表明它们代表结缔组织基质中的非增殖细胞群。目前的研究结果可能有助于将迄今为止文献中分别发现的关于FXIII A和巨噬细胞在结缔组织形成中的作用的理论联系起来。
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Accumulation of cells containing factor XIII subunit a around the foci of intense fibrosis in human epulides.

On the basis of clinical and biochemical findings, Factor XIII subunit a (FXIII A) has been conjectured to play an important role in fibrotic processes. Epulis samples at different stages of fibrotic tissue formation were used as a model system for studying the localization and tissue distribution of FXIII A during the course of connective tissue generation. Marker characteristics of cells containing FXIII A (FXIII A+ cells) were determined as well. In double immunofluorescent labelling systems, FXIII A was localized in monocyte-derived (CD-14+), activated (HLA-DR+), and phagocytosing (Ki-M7+) tissue macrophages, which are widely distributed homogeneously in granulation tissues, but start to accumulate around foci of fibrosis as soon as the foci appear. During the relatively long process of fibrosis, FXIII A+ macrophages continuously decrease in number, and their morphological appearance changes from stellate to spindle-shaped. The nuclei of these cells were not labelled by Ki-67 monoclonal antibody; this indicating that they represent a non-proliferating cell population in the connective tissue stroma. The present findings may help to link theories concerning the role of FXIII A and those of macrophages in the connective tissue formation so far found separately in the literature.

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