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4β,15-二乙酰氧基镰刀菌烯醇在体外诱导鸡巨噬细胞产生细胞毒性,并改变其吞噬和Fc受体表达功能。

4 beta, 15-Diacetoxyscirpenol induces cytotoxicity and alterations in phagocytic and Fc-receptor expression functions in chicken macrophages in vitro.

作者信息

Qureshi M A, Brundage M A, Hamilton P B

机构信息

Department of Poultry Science, North Carolina State University, Raleigh 27695-7608, USA.

出版信息

Immunopharmacol Immunotoxicol. 1998 Nov;20(4):541-53. doi: 10.3109/08923979809031515.

DOI:10.3109/08923979809031515
PMID:9805233
Abstract

4 beta, 15 Diacetoxyscirpenol (DAS) mycotoxin produced by Fusarium species was tested for detrimental effects on macrophage viability, phagocytosis, and Fc-receptor expression. Sephadex-elicited chicken abdominal cells were harvested to establish adherent macrophage monolayers on glass coverslips. Coverslips were then assigned randomly to treatment groups (0, 12.5 and 25 micrograms/mL DAS). Macrophage monolayers were exposed to treatments for 1 h, washed, and tested for various functional endpoints. Treatment with DAS resulted in decreased viability of macrophages (90.8% vs 81.5% vs 70.4% viable in the 0, 12.5 and 25 micrograms treatments, respectively) and decreased the percentage of macrophages phagocytizing sheep erythrocytes (81.6% vs 53.1% vs 46.0%. DAS also caused a decrease in the mean number of opsonized cells engulfed per phagocytic macrophage (5.7 vs 3.7 vs 2.9). A similar trend was observed using unopsonized sheep erythrocytes (15.4% vs 7.6% vs 5.5% phagocytic macrophages and 0.29 vs 0.11 vs 0.08 erythrocytes engulfed per macrophage). The incidence of Fc-receptor positive macrophages determined by sheep erythrocyte rosetting was also decreased in DAS-treated macrophages as compared to the control (49.2% vs 32.7% vs 24.2%). The findings of this study demonstrate that DAS exposure causes a suppression in macrophage phagocytic function and therefore may alter the first line of immunological defense in chickens.

摘要

对镰刀菌属产生的4β,15-二乙酰氧基雪腐镰刀菌烯醇(DAS)霉菌毒素对巨噬细胞活力、吞噬作用及Fc受体表达的有害影响进行了检测。采集葡聚糖诱导的鸡腹部细胞,在玻璃盖玻片上建立贴壁巨噬细胞单层。然后将盖玻片随机分配至各处理组(0、12.5和25微克/毫升DAS)。巨噬细胞单层经处理1小时后,洗涤并检测各种功能终点指标。用DAS处理导致巨噬细胞活力下降(在0、12.5和25微克处理组中,存活细胞分别为90.8%、81.5%和70.4%),吞噬绵羊红细胞的巨噬细胞百分比降低(81.6%、53.1%和46.0%)。DAS还导致每个吞噬性巨噬细胞吞噬的调理细胞平均数量减少(5.7、3.7和2.9)。使用未调理的绵羊红细胞时观察到类似趋势(吞噬性巨噬细胞分别为15.4%、7.6%和5.5%,每个巨噬细胞吞噬的红细胞分别为0.29、0.11和0.08)。与对照组相比,经DAS处理的巨噬细胞中通过绵羊红细胞花环试验测定的Fc受体阳性巨噬细胞发生率也降低(49.2%、32.7%和24.2%)。本研究结果表明,接触DAS会导致巨噬细胞吞噬功能受到抑制,因此可能改变鸡的第一道免疫防线。

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