首页> 外文期刊>Molecular and Cellular Biochemistry: An International Journal for Chemical Biology >Involvement of the nuclear factor-κB pathway in the adhesion of neutrophils to renal tubular cells after injury induced by neonatal postasphyxial serum
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Involvement of the nuclear factor-κB pathway in the adhesion of neutrophils to renal tubular cells after injury induced by neonatal postasphyxial serum

机译:新生儿窒息后血清损伤后核因子-κB通路参与中性粒细胞与肾小管细胞的粘附

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Nuclear factor κB (NF-κB) plays an important role in the regulation of inflammatory proteins. However, it is unclear whether the NF-κB/intercellular adhesion molecule-1 (ICAM-1) pathway is involved in the adhesion of neutrophils and renal injury after hypoxia-ischemia (HI) in neonates. In this report we investigated whether NF-κB and its downstream molecule ICAM-1 were involved in renal injury induced by postasphyxial serum (PS) from neonates. Human renal proximal tubular (HK-2) cells were preincubated with 10 % fetal calf serum (control), 20 % neonatal PS, or 20 % PS plus pyrolidine dithiocarbamate (PDTC). The expression of IκBα, NF-κB p65, and ICAM-1 in HK-2 cells was determined by Western blot and/or immunohistochemistry. Nuclear translocation of NF-κB p65 in HK-2 cells was detected by immunofluorescence and Western blot. The ICAM-1 mRNA was determined by RT-PCR. Then HK-2 cells were cultured with neutrophils from neonates with asphyxia. After HK-2 cells had been cultured with neutrophils, we detected myeloperoxidase (MPO) activity, the leakage rate of lactate dehydrogenase (LDH), and cell viability. We found that PS preincubation resulted in significantly decreased IκBα expression and increased expression of NF-κB and ICAM-1, and facilitated the nuclear translocation of NF-κB in HK-2 cells. PS preincubation increased MPO activity, leading to elevated leakage rates of LDH and decreased cell viability after neutrophil exposure. Furthermore, the inhibition of NF-κB activity by PDTC significantly upregulated IκBα expression, decreased NF-κB and ICAM-1 expression, downregulated the nuclear translocation of NF-κB, and decreased MPO activity. This leads to decreased leakage rates of LDH and increased cell viability after neutrophil exposure. Our findings suggest that NF-κB/ICAM-1 pathway may be involved in neutrophil-endothelial interactions and neonatal renal injury after HI.
机译:核因子κB(NF-κB)在调节炎症蛋白中起重要作用。然而,尚不清楚NF-κB/细胞间粘附分子-1(ICAM-1)通路是否参与新生儿缺氧缺血(HI)后中性粒细胞的粘附和肾损伤。在本报告中,我们调查了NF-κB及其下游分子ICAM-1是否参与新生儿窒息后血清(PS)诱发的肾损伤。将人肾近端肾小管(HK-2)细胞与10%胎牛血清(对照),20%新生儿PS或20%PS加吡咯烷二硫代氨基甲酸酯(PDTC)一起孵育。 Western blot和/或免疫组化法检测HK-2细胞中IκBα,NF-κBp65和ICAM-1的表达。通过免疫荧光和蛋白质印迹检测HK-2细胞中NF-κBp65的核易位。通过RT-PCR确定ICAM-1 mRNA。然后用窒息新生儿的嗜中性白细胞培养HK-2细胞。 HK-2细胞与嗜中性粒细胞培养后,我们检测了髓过氧化物酶(MPO)活性,乳酸脱氢酶(LDH)的泄漏率和细胞活力。我们发现PS预孵育导致HK-2细胞中IκBα表达明显降低,NF-κB和ICAM-1表达增加,并促进NF-κB的核易位。 PS预孵育会增加MPO活性,导致中性粒细胞暴露后LDH的漏出率升高,细胞活力降低。此外,PDTC对NF-κB活性的抑制作用显着上调了IκBα的表达,降低了NF-κB和ICAM-1的表达,下调了NF-κB的核转运,并降低了MPO活性。这导致中性粒细胞暴露后LDH的漏出率降低和细胞活力增加。我们的发现提示,HI后NF-κB/ ICAM-1途径可能与中性粒细胞-内皮相互作用和新生儿肾损伤有关。

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