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抗原表达的异质性解释了小鼠肾小球肾炎中肾小球巨噬细胞积聚存在争议的原因。

Heterogeneity of antigen expression explains controversy over glomerular macrophage accumulation in mouse glomerulonephritis.

作者信息

Masaki Takao, Chow Fiona, Nikolic-Paterson David J, Atkins Robert C, Tesch Gregory H

机构信息

Department of Nephrology, Monash Medical Centre, Clayton, Victoria, Australia.

出版信息

Nephrol Dial Transplant. 2003 Jan;18(1):178-81. doi: 10.1093/ndt/18.1.178.

Abstract

BACKGROUND

Many antibody labelling studies have suggested that there are few or no glomerular macrophages in mouse models of glomerulonephritis, despite the presence of a prominent interstitial macrophage infiltrate. These findings conflict with studies of human and rat glomerulonephritis. Therefore, we examined whether heterogeneity of macrophage antigen expression could explain this apparent discrepancy.

METHODS

Kidneys were collected from normal mice and mice killed at 2 and 10 days after induction of accelerated anti-glomerular basement membrane (GBM) glomerulonephritis. Following fixation, macrophages were detected by immunoperoxidase staining in serial kidney sections using antibodies recognising CD11b, F4/80 and CD68.

RESULTS

Induction of anti-GBM nephritis caused a progressive increase in glomerular and interstitial leukocytes. At days 2 and 10, there were more CD68+ macrophages in glomeruli than macrophages expressing CD11b or F4/80. At day 10, CD68+ macrophages accounted for almost all glomerular CD45+ total leukocytes. In contrast, CD11b+ and F4/80+ macrophages at day 10 accounted for only 65 and 13% of glomerular leukocytes, respectively. However, in the interstitium the number of macrophages expressing CD68, CD11b and F4/80 were not different.

CONCLUSION

Antibody detection of mouse CD68 identifies all glomerular macrophages in mouse anti-GBM nephritis, indicating a similar infiltrate to that seen in human and rat anti-GBM nephritis. Our finding of substantial heterogeneity in glomerular macrophage antigen expression in this model suggests that previous studies of mouse glomerulonephritis may have underestimated glomerular macrophages and their role in glomerular injury.

摘要

背景

许多抗体标记研究表明,在肾小球肾炎的小鼠模型中,尽管存在明显的间质巨噬细胞浸润,但肾小球巨噬细胞很少或不存在。这些发现与人类和大鼠肾小球肾炎的研究结果相矛盾。因此,我们研究了巨噬细胞抗原表达的异质性是否可以解释这一明显差异。

方法

从正常小鼠以及诱导加速抗肾小球基底膜(GBM)肾小球肾炎后2天和10天处死的小鼠中收集肾脏。固定后,使用识别CD11b、F4/80和CD68的抗体,通过免疫过氧化物酶染色在连续的肾脏切片中检测巨噬细胞。

结果

抗GBM肾炎的诱导导致肾小球和间质白细胞逐渐增加。在第2天和第10天,肾小球中CD68+巨噬细胞比表达CD11b或F4/80的巨噬细胞更多。在第10天,CD68+巨噬细胞几乎占所有肾小球CD45+总白细胞的全部。相比之下,第10天时CD11b+和F4/80+巨噬细胞分别仅占肾小球白细胞的65%和13%。然而,间质中表达CD68、CD11b和F4/80的巨噬细胞数量没有差异。

结论

小鼠CD68的抗体检测可识别小鼠抗GBM肾炎中所有的肾小球巨噬细胞,表明其浸润情况与人类和大鼠抗GBM肾炎相似。我们在该模型中发现肾小球巨噬细胞抗原表达存在显著异质性,这表明先前对小鼠肾小球肾炎的研究可能低估了肾小球巨噬细胞及其在肾小球损伤中的作用。

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