Vyalov S, Desmoulière A, Gabbiani G
University of Geneva, Department of Pathology, CMU, Switzerland.
Virchows Arch B Cell Pathol Incl Mol Pathol. 1993;63(4):231-9. doi: 10.1007/BF02899267.
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.
我们使用电子显微镜以及光镜和电镜水平的免疫组织化学方法,利用抗α平滑肌(SM)肌动蛋白和大鼠巨噬细胞的特异性抗体,按时间顺序研究了在大鼠体内递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。在泵植入后2天和3天,GM-CSF的应用引发了广泛的炎症反应,其特征为水肿以及多形核细胞和巨噬细胞的聚集。逐渐地,多形核细胞数量减少,巨噬细胞开始聚集成大簇。肉芽组织成纤维细胞中α-SM肌动蛋白的表达从泵植入后第4天开始,并持续至第7天。双重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。电子显微镜检查证实,最初在聚集的巨噬细胞附近发现含有α-SM肌动蛋白阳性应力纤维的成纤维细胞。渗透微型泵递送血小板衍生生长因子(PDGF)和肿瘤坏死因子-α(TNF-α)会诱导巨噬细胞聚集,但与GM-CSF应用后相比数量要少得多;这些巨噬细胞从未聚集成簇,此外,TNF-α和PDGF并未刺激成纤维细胞中α-SM肌动蛋白的表达。我们的结果表明,GM-CSF给药后,巨噬细胞的簇状聚集在刺激肌成纤维细胞中α-SM肌动蛋白表达方面发挥重要作用。我们的结果可能有助于理解在此实验模型及其他实验模型中导致肉芽组织形成的过程。