Sunderkötter C, Beil W, Roth J, Sorg C
Institute of Experimental Dermatology, University of Münster, Federal Republic of Germany.
Am J Pathol. 1991 Apr;138(4):931-9.
The aim of this study was to establish an angiogenesis model in the mouse and to define immunohistochemically the cellular events that precede angiogenesis. After chemical cauterization of the murine cornea, neovascularization was observed within 36 hours. The cellular infiltrate was analyzed by using antibodies on cryostat and paraffin sections and by histochemical staining for mast cells. It was found that neither T lymphocytes nor mast cells nor macrophages in a more mature stage of development were part of the infiltrate that preceded the ingrowth of new blood vessels. Instead, the infiltrating cells appearing from 3 hours on were granulocytes and inflammatory monocytes, as detected by an antibody against the calcium-binding protein MRP14. The authors conclude that the induction of angiogenesis during nonspecific inflammation is associated with the early influx of myelomonocytic cells, but not with the infiltration of mature macrophages, T lymphocytes, or mast cells. This study shows that immunohistochemical analysis of cauterized murine corneas presents a useful tool for further studies on cells and cell products involved in the angiogenic process.
本研究的目的是在小鼠中建立血管生成模型,并通过免疫组织化学方法确定血管生成之前的细胞事件。对小鼠角膜进行化学烧灼后,在36小时内观察到了新血管形成。通过在低温恒温器切片和石蜡切片上使用抗体以及对肥大细胞进行组织化学染色来分析细胞浸润情况。结果发现,在新血管长入之前的浸润细胞中,既没有T淋巴细胞,也没有肥大细胞或处于更成熟发育阶段的巨噬细胞。相反,从3小时开始出现的浸润细胞是粒细胞和炎性单核细胞,这是通过一种针对钙结合蛋白MRP14的抗体检测到的。作者得出结论,非特异性炎症期间血管生成的诱导与骨髓单核细胞的早期流入有关,而与成熟巨噬细胞、T淋巴细胞或肥大细胞的浸润无关。这项研究表明,对烧灼后的小鼠角膜进行免疫组织化学分析为进一步研究血管生成过程中涉及的细胞和细胞产物提供了一个有用的工具。