RNF43 p.G659fs 通过 PI3K/AKT/mTOR 信号通路和 HLA-E 上调导致 MSI-high 结直肠癌中 NK 细胞功能障碍
RNF43 p.G659fs leads to natural killer cell dysfunction in MSI-high colorectal cancer through PI3K/AKT/mTOR signaling and HLA-E up-regulation.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Immunotoxicity studies of sulfolane following developmental exposure in Hsd:Sprague Dawley SD rats and adult exposure in B6C3F1/N mice.
Immunotoxicity studies of sulfolane following developmental exposure in Hsd:Sprague Dawley SD rats and adult exposure in B6C3F1/N mice.
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砜是一种石化工业使用的溶剂,也是炼油厂附近地区的地下水污染物。本研究采用两种模型评估口服砜暴露对免疫系统的影响:(1)围产期饮水暴露模型:从妊娠第6天起至13周龄,Harlan Sprague Dawley大鼠饮用含0、30、100、300或1000 mg/L砜的水;(2)90天灌胃暴露模型:成年雌性B6C3F1/N小鼠每日接受0、1、10、30、100或300 mg/kg砜。评估的免疫参数包括抗绵羊红细胞(SRBC)和钥孔𫚉血蓝蛋白(KLH)抗体的产生、离体自然杀伤(NK)细胞活性、细胞毒性T细胞(CTL)活性和T细胞增殖,以及脾脏免疫细胞群、血液学参数和免疫组织组织病理学。发育期暴露后,雌性F1大鼠细胞的离体NK活性降低,雄性则未见此变化。成年雌鼠中,100 mg/kg剂量组脾NK细胞数量低于溶媒对照组;然而,砜处理未影响离体NK细胞活性。雌鼠中,30 mg/kg剂量组大型未染色细胞数量降低。F1大鼠白细胞(WBC)变化仅表现为雌性白细胞减少趋势;雄性未见影响。根据雌性F1大鼠NK细胞活性下降,本研究条件下确定的未观察到作用水平(NOEL)为3 mg/kg/天。
总体而言,这些结果提示,啮齿动物口服砜对免疫系统的影响很小。
Sulfolane is a solvent used in the petrochemical industry and a groundwater contaminant in areas near refineries. The current studies were conducted to assess the impact of oral exposure to sulfolane on the immune system using two models: (1) a perinatal drinking water exposure to 0, 30, 100, 300, or 1000 mg/L from gestation day (GD) 6 until 13 weeks-of-age in Harlan Sprague Dawley rats; and, (2) a 90-day gavage exposure of adult female B6C3F1/N mice to 0, 1, 10, 30, 100, or 300 mg/kg/day. Immune parameters evaluated included measurement of antibody production against sheep red blood cells (SRBC) and keyhole limpet hemocyanin (KLH), ex vivo measurements of natural killer (NK) cell activity, cytotoxic T-cell (CTL) activity, and T-cell proliferation, as well as measures of splenic immune cell populations, hematological parameters, and histopathology of immune tissues.
A decrease in ex vivo NK cell activity was observed in cells from female - but not male - F1 rats following developmental exposure. In adult female mice, splenic NK cell number was lower than the vehicle controls at doses 100 mg/kg; however, ex vivo NK cell activity was not affected by sulfolane treatment.
In female mice, a decrease in the number of large unstained cells at doses 30 mg/kg was observed. In F1 rats, effects on white blood cells (WBC) were limited to a decreasing trend in leukocytes in females; no effects were observed in males. Under the conditions of this study, a no-observed-effect level (NOEL) of 3 mg/kg/day was identified based on reduced NK cell activity in female F1 rats.
Overall, these findings suggest that oral exposure to sulfolane in rodents had minimal effects on the immune system.
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