Prasad Priyanka, Sinha Dona
Department of Receptor Biology and Tumor Metastasis, Chittaranjan National Cancer Institute, 37, S.P. Mukherjee Road, Kolkata, 700 026, India.
Environ Sci Pollut Res Int. 2017 Apr;24(12):11708-11721. doi: 10.1007/s11356-017-8744-8. Epub 2017 Mar 22.
The impact of chronic low-level groundwater arsenic (As) exposure [in the range above the WHO-recommended limit of 10 μg/L but ≤50 μg/L (permissible limit of As for many Asian countries)] was investigated for cross talk of inflammatory changes and expression of phagocytic receptors of exposed rural women (N, 45) from districts of 24 Parganas (south) and in matched control groups (N, 43) [As ≤10 μg/L] from the same district. Systemic inflammation was evident from the upregulated levels of pro-inflammatory mediators like tumor necrosis factor-α (TNF-α); interleukins (ILs) like IL-6, IL-8, and IL-12; and C-reactive protein (CRP) in the sera and upregulated expression of protein kinase B phosphorylated at ser473 (pAKTser473)/nuclear factor-κB (NF-κB)/TNF-α axis in the leukocytes of exposed women with respect to control. We found that low-dose As exposure apart from inflicting inflammation altered the expression of phagocytic receptors-Fcγ receptors (FcγRs) and complement receptors (CRs). The leukocytes of the low-As-exposed women exhibited suppression of CD64, CD35, and CD11b and increased expression of CD16 with respect to control. Groundwater As showed a negative correlation with CD64 expression on monocytes [Pearson's r, -0.8205; 95% confidence interval (CI), -0.8789 to -0.7379] and granulocytes [r, -0.7635; 95% CI, -0.8388 to -0.6595] and a positive correlation with CD16 on granulocytes [r, 0.8363; 95% CI, 0.7599 to 0.8899]. A negative correlation of groundwater As was also observed with expression of CD35 on granulocytes [r, -0.8780; 95% CI, -0.9185 to -0.8192] and monocytes [r, -0.7778; 95% CI, -0.8490 to -0.6790] and CD11b on monocytes [r, -0.6035; 95% CI, -0.7218 to -0.4511]. Therefore, it may be indicated that chronic low-level As exposure (11-50 μg/L) not only evoked chronic inflammatory changes but also suppressed the expression of FcγRs and CRs in the exposed women. This, in turn, may lead to susceptibility towards pathogenic infections or in long run may even contribute towards chronic inflammatory diseases including cancer.
研究了长期低水平地下水砷(As)暴露[暴露水平高于世界卫生组织推荐的10μg/L限值但≤50μg/L(许多亚洲国家的As允许限值)]对来自24 Parganas(南部)地区的农村暴露女性(N = 45)以及同一地区匹配对照组(N = 43)[As≤10μg/L]的炎症变化和吞噬细胞受体表达的相互影响。从血清中促炎介质如肿瘤坏死因子-α(TNF-α)、白细胞介素(ILs)如IL-6、IL-8和IL-12以及C反应蛋白(CRP)水平上调,以及暴露女性白细胞中丝氨酸473磷酸化的蛋白激酶B(pAKTser473)/核因子-κB(NF-κB)/TNF-α轴的表达上调可以明显看出全身炎症。我们发现,低剂量As暴露除了引发炎症外,还改变了吞噬细胞受体——Fcγ受体(FcγRs)和补体受体(CRs)的表达。与对照组相比,低As暴露女性的白细胞表现出CD64、CD35和CD11b的表达受到抑制,而CD16的表达增加。地下水中的As与单核细胞[Pearson相关系数r = -0.8205;95%置信区间(CI),-0.8789至-0.7379]和粒细胞[r = -0.7635;95%CI,-0.8388至-0.6595]上CD64的表达呈负相关,与粒细胞上CD16的表达呈正相关[r = 0.8363;95%CI,0.7599至0.8899]。还观察到地下水中的As与粒细胞[r = -0.8780;95%CI,-0.9185至-0.8192]和单核细胞[r = -0.7778;95%CI,-0.8490至-0.6790]上CD35的表达以及单核细胞上CD11b的表达[r = -0.6035;95%CI,-0.7218至-0.4511]呈负相关。因此,可能表明长期低水平As暴露(11 - 50μg/L)不仅引发慢性炎症变化,还抑制了暴露女性中FcγRs和CRs 的表达。这反过来可能导致对病原体感染的易感性,从长远来看甚至可能导致包括癌症在内的慢性炎症性疾病。