发育中小鼠肝脏库普弗氏细胞的表征。

Bryan G Lopez, Monica S Tsai, Janie L Baratta, Kenneth J Longmuir, Richard T Robertson
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引用次数: 66

摘要

背景:库普弗细胞是众所周知的肝脏巨噬细胞,然而,小鼠库普弗细胞的发育特征尚不清楚。为了阐明这一问题,我们利用光镜和免疫细胞化学研究了正常发育小鼠肝脏中库普弗巨噬细胞的特征。方法:采用免疫细胞化学技术制备早期产后小鼠肝组织切片。通过对F4/80抗体的免疫反应性鉴定库普弗细胞,而内皮细胞用CD-34抗体标记。此外,通过全身注射荧光标记乳胶微球对库普弗细胞和内皮细胞进行标记。荧光显微镜观察组织切片。结果:静脉注射或腹腔内注射微球产生相似的肝细胞标记模式。F4/80阳性Kupffer细胞分别用大直径(0.2 μm)和小直径(0.02 μm)微球进行标记,内皮细胞仅用直径较小的微球进行标记。Kupffer细胞的微球标记至少在6周内保持稳定。早在出生后第0天就发现了对F4/80有免疫反应的细胞,这些细胞也表现出对微球的摄取。F4/80 Kupffer细胞的数量,相对于白蛋白阳性肝细胞的数量,在出生后的前2周没有明显的变化趋势。结论:发育中的小鼠肝脏的Kupffer细胞与其他哺乳动物非常相似,证实了小鼠是研究肝巨噬细胞发育结构和功能的有用动物模型。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Characterization of Kupffer cells in livers of developing mice.

Background: Kupffer cells are well known macrophages of the liver, however, the developmental characteristics of Kupffer cells in mice are not well understood. To clarify this matter, the characteristics of Kupffer macrophages in normal developing mouse liver were studied using light microscopy and immunocytochemistry.

Methods: Sections of liver tissue from early postnatal mice were prepared using immunocytochemical techniques. The Kupffer cells were identified by their immunoreactivity to the F4/80 antibody, whereas endothelial cells were labelled with the CD-34 antibody. In addition, Kupffer cells and endothelial cells were labelled by systemically injected fluorescently labelled latex microspheres. Tissue slices were examined by fluorescence microscopy.

Results: Intravenous or intraperitonal injections of microspheres yielded similar patterns of liver cell labelling. The F4/80 positive Kupffer cells were labelled with both large (0.2 μm) and small (0.02 μm) diameter microspheres, while endothelial cells were labelled only with the smaller diameter microspheres. Microsphere labelling of Kupffer cells appeared stable for at least 6 weeks. Cells immunoreactive for F4/80 were identified as early as postnatal day 0, and these cells also displayed uptake of microspheres. Numbers of F4/80 Kupffer cells, relative to numbers of albumin positive hepatocytes, did not show a significant trend over the first 2 postnatal weeks.

Conclusions: Kupffer cells of the developing mouse liver appear quite similar to those of other mammalian species, confirming that the mouse presents a useful animal model for studies of liver macrophage developmental structure and function.

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