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炎症诱导大鼠腹膜炎模型中细胞半乳糖凝集素-1和-3表达的调节

Inflammation-induced modulation of cellular galectin-1 and -3 expression in a model of rat peritonitis.

作者信息

Gil C D, Cooper D, Rosignoli G, Perretti M, Oliani S M

机构信息

Department of Anatomy, Faculty of Medicine (FAMERP), Av. Brigadeiro Faria Lima 5416, 15090-000, São José do Rio Preto, SP, Brazil.

出版信息

Inflamm Res. 2006 Mar;55(3):99-107. doi: 10.1007/s00011-005-0059-4.

Abstract

OBJECTIVE AND DESIGN

To investigate the effect of galectin-1 (Gal-1) and -3 (Gal-3) on leukocyte migration and analyze the expression of both galectins in inflammatory cells using a model of rat peritonitis.

MATERIAL OR SUBJECTS

Sprague-Dawley rats (n = 4 per group).

TREATMENT

Peritonitis was induced in animals through intraperitoneal injection of carrageenin (1.5 mg/kg) and rat mesenteries were analyzed at different time points (0, 4, 24 and 48h). For pharmacological treatment, rats received intravenous injection of Gal-1 or -3 (3microg/kg) followed by carrageenin.

METHODS

Western blotting and immunoelectron microscopy analysis. Statistical analysis was performed using ANOVA followed by Bonferroni test.

RESULTS

Pharmacological treatment with Gal-1, but not Gal-3, inhibited (approximately 50 %) leukocyte recruitment into the peritoneal cavity at 4 h time-point. In this early phase, immunogold staining of mesenteries showed a diminished Gal-3 expression in degranulated mast cells and Gal-1 in transmigrated neutrophils (approximately 20 % reduction compared to intravascular cells). In the later phases (24 and 48h), leukocyte turnover was associated with augmented Gal-1 expression in neutrophils and macrophages and Gal-3 in mast cells and macrophages.

CONCLUSIONS

These results point to a balanced expression of cell-associated-Gal-1/Gal-3 and might impact on the development of new therapeutic strategies for inflammatory diseases.

摘要

目的与设计

利用大鼠腹膜炎模型,研究半乳糖凝集素-1(Gal-1)和-3(Gal-3)对白细胞迁移的影响,并分析这两种半乳糖凝集素在炎症细胞中的表达。

材料或对象

Sprague-Dawley大鼠(每组n = 4)。

处理

通过腹腔注射角叉菜胶(1.5 mg/kg)诱导动物发生腹膜炎,并在不同时间点(0、4、24和48小时)分析大鼠肠系膜。对于药物治疗,大鼠先静脉注射Gal-1或-3(3μg/kg),随后注射角叉菜胶。

方法

蛋白质免疫印迹法和免疫电子显微镜分析。采用方差分析及Bonferroni检验进行统计学分析。

结果

Gal-1药物治疗而非Gal-3药物治疗在4小时时间点抑制了(约50%)白细胞向腹腔的募集。在这个早期阶段,肠系膜的免疫金染色显示,脱颗粒肥大细胞中Gal-3表达减少,迁移的中性粒细胞中Gal-1表达减少(与血管内细胞相比约减少20%)。在后期阶段(24和48小时),白细胞更新与中性粒细胞和巨噬细胞中Gal-1表达增加以及肥大细胞和巨噬细胞中Gal-3表达增加相关。

结论

这些结果表明细胞相关Gal-1/Gal-3表达平衡,可能会影响炎症性疾病新治疗策略的开发。

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