Toida M, Oka N, Takami T, Adány R
Department of Oral Surgery and Oral Medicine, Ibi General Hospital, Japan.
Histochem J. 1995 Jun;27(6):440-8.
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.
基于临床和生化研究结果,推测凝血因子 XIII a 亚基(FXIII A)在纤维化过程中发挥重要作用。将纤维化组织形成不同阶段的牙龈瘤样本作为模型系统,用于研究结缔组织生成过程中 FXIII A 的定位和组织分布。同时也确定了含有 FXIII A 的细胞(FXIII A+细胞)的标记特征。在双重免疫荧光标记系统中,FXIII A 定位于单核细胞衍生的(CD-14+)、活化的(HLA-DR+)和吞噬的(Ki-M7+)组织巨噬细胞中,这些巨噬细胞在肉芽组织中广泛均匀分布,但一旦纤维化病灶出现,就开始在纤维化病灶周围积聚。在相对较长的纤维化过程中,FXIII A+巨噬细胞数量持续减少,其形态从星状变为梭形。这些细胞的细胞核未被 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体。目前的研究结果可能有助于将有关 FXIII A 作用的理论与巨噬细胞在结缔组织形成中的作用理论联系起来,而这些理论在迄今为止的文献中是分别发现的。