gm - csf诱导的肉芽组织形成:巨噬细胞与肌成纤维细胞积累之间的关系。

S Vyalov, A Desmoulière, G Gabbiani
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引用次数: 110

摘要

我们使用电子显微镜和免疫组织化学在光镜和电子显微镜水平上研究了大鼠输送粒细胞巨噬细胞集落刺激因子(GM-CSF)的渗透微型泵周围肉芽组织的形成,并使用针对α -平滑肌(SM)肌动蛋白和大鼠巨噬细胞的特异性抗体。在泵植入后2和3天,GM-CSF应用产生以水肿和多形核细胞和巨噬细胞积聚为特征的广泛炎症反应。逐渐地,多形核细胞数量减少,巨噬细胞呈大簇状排列。α - sm肌动蛋白在肉芽组织成纤维细胞中的表达从泵植入后第4天开始,持续到第7天。双免疫荧光染色显示巨噬细胞簇与富含α - sm肌动蛋白的成纤维细胞有关。电镜检查证实含有α - sm肌动蛋白阳性应激纤维的成纤维细胞最初是在群集巨噬细胞附近发现的。通过渗透性微型泵输送血小板衍生生长因子(PDGF)和肿瘤坏死因子- α (tnf - α)诱导巨噬细胞的积累,但与GM-CSF应用后相比,巨噬细胞的数量要少得多;这些巨噬细胞从未聚集成簇,此外,tnf - α和PDGF不会刺激成纤维细胞中α - sm肌动蛋白的表达。我们的研究结果表明,GM-CSF给药后,巨噬细胞的簇状积聚在刺激肌成纤维细胞中α - sm肌动蛋白的表达中起重要作用。我们的结果可能与理解导致肉芽组织形成的过程有关,在这个和其他实验模型中。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
GM-CSF-induced granulation tissue formation: relationships between macrophage and myofibroblast accumulation.

We have studied the formation of granulation tissue around osmotic minipumps delivering granulocyte macrophage-colony stimulating factor (GM-CSF) chronologically in the rat using electron microscopy and immunohistochemistry at the light and electron microscopic levels, with specific antibodies against alpha-smooth muscle (SM) actin and rat macrophages. At 2 and 3 days after pump implantation, GM-CSF application produced an extensive inflammatory reaction characterized by edema and the accumulation of polymorphonuclear cells and macrophages. Gradually, polymorphonuclear cells decreased in number and macrophages became arranged in large clusters. The expression of alpha-SM actin in fibroblastic cells of the granulation tissue started from the 4th day after pump implantation and progressed up to the 7th day. Double immunofluorescence staining showed macrophage clusters in relation to alpha-SM actin-rich fibroblastic cells. Electron microscopic examination confirmed that the fibroblasts containing alpha-SM actin-positive stress fibers were found initially in close proximity to clustered macrophages. The delivery of platelet-derived growth factor (PDGF) and tumor necrosis factor-alpha (TNF-alpha) by the osmotic minipump induced an accumulation of macrophages, but in a much smaller number compared with those seen after GM-CSF application; these macrophages were never assembled in clusters and, furthermore, TNF-alpha and PDGF did not stimulate alpha-SM actin expression in fibroblastic cells. Our results suggest that after GM-CSF administration, the cluster-like accumulation of macrophages plays an important role in stimulating alpha-SM actin expression in myofibroblasts. Our results may be relevant to the understanding of the processes leading to granulation tissue formation in this and other experimental models.

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