Stermer Angela R, Murphy Caitlin J, Ghaffari Rashin, Di Bona Kristin R, Voss Jorine J, Richburg John H
Center for Molecular Carcinogenesis and Toxicology, College of Pharmacy, The University of Texas at Austin, Austin, TX 78712, United States.
Center for Molecular Carcinogenesis and Toxicology, College of Pharmacy, The University of Texas at Austin, Austin, TX 78712, United States.
Reprod Toxicol. 2017 Apr;69:150-158. doi: 10.1016/j.reprotox.2017.02.013. Epub 2017 Feb 24.
Exposure of rodents to the Sertoli cell (SC) toxicant mono-(2-ethylhexyl) phthalate (MEHP) has been reported to trigger an infiltration of macrophages into the testis in an age- and species-dependent manner. Here we challenge the hypothesis that the peripubertal rat-specific infiltration of macrophages after MEHP exposure is due, in part, to an increase in SC-specific inflammatory cytokine expression. To rule out that germ cell(GC) apoptosis itself is responsible for macrophage recruitment, rats were exposed to a direct GC toxicant, methoxyacetic acid (MAA), but no infiltration of macrophages was observed. Next, mRNA levels of inflammatory cytokines were evaluated after MEHP exposure. IL-1α, IL-6, and MCP-1 expression were increased in vivo and correlated with macrophage infiltration in a species-specific manner. Additionally, IL-6 and MCP-1 expression was increased in SC-GC co-cultures and ASC-17D SCs. These results indicate that MEHP-injury in pubertal rats specifically stimulates secretion of pro-inflammatory cytokines and alters the immune microenvironment.
据报道,啮齿动物暴露于支持细胞(SC)毒性物质邻苯二甲酸单(2-乙基己基)酯(MEHP)会以年龄和物种依赖的方式引发巨噬细胞浸润到睾丸中。在此,我们对以下假设提出质疑:MEHP暴露后青春期前大鼠特异性的巨噬细胞浸润部分归因于SC特异性炎性细胞因子表达的增加。为了排除生殖细胞(GC)凋亡本身导致巨噬细胞募集的可能性,将大鼠暴露于直接的GC毒性物质甲氧基乙酸(MAA),但未观察到巨噬细胞浸润。接下来,评估MEHP暴露后炎性细胞因子的mRNA水平。白细胞介素-1α(IL-1α)、白细胞介素-6(IL-6)和单核细胞趋化蛋白-1(MCP-1)的表达在体内增加,并以物种特异性方式与巨噬细胞浸润相关。此外,在SC-GC共培养物和ASC-17D支持细胞中,IL-6和MCP-1的表达也增加。这些结果表明,青春期大鼠的MEHP损伤特异性地刺激促炎细胞因子的分泌,并改变免疫微环境。