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与外周血(PB)单个核细胞相比,脐血(CB)单个核细胞中白细胞介素-18(IL-18)基因表达和蛋白产生不成熟,以及对自然杀伤(NK)细胞发育和功能的不同影响。

Immaturity of IL-18 gene expression and protein production in cord blood (CB) versus peripheral blood (PB) mononuclear cells and differential effects in natural killer (NK) cell development and function.

作者信息

Satwani Prakash, Ayello Janet, Ven Carmella, O'Neill Allison F, Simpson Lynn L, Baxi Laxmi, Cairo Mitchell S

机构信息

Department of Pediatrics, Columbia University, New York, NY, USA.

出版信息

Br J Haematol. 2005 Jul;130(2):284-92. doi: 10.1111/j.1365-2141.2005.05592.x.

Abstract

We have previously demonstrated dysregulation of IL-12 and IL-15 gene and protein expression between activated cord blood (CB) versus peripheral blood (PB) mononuclear cells (MNCs). In the present study, we compared IL-18 gene expression and protein production and IL-18 mRNA half-life in basal versus activated CB versus PB MNCs, the effects of IL-18 +/- IL-12 on MNCs IFN-gamma protein production and ex vivo expansion and activation of CB with IL-12 + IL-2 + anti-CD3 +/- IL-18. Basal and activated levels of IL-18 were significantly higher in PB versus CB MNCs (P < 0.05). IL-18 mRNA was coincidental with protein levels and significantly lower in CB (P < 0.05) and its half-life significantly shorter in CB versus PB MNCs (P < 0.05). IL-18 synergistically with IL-12 induced IFN-gamma production from PB greater than CB MNCs (P < 0.05). NK cells expansion (P < 0.001) and cytotoxicity (P < 0.01) was significantly increased with IL-12 + IL-2 + anti-CD3 and IL-18. In summary IL-18 gene expression and protein production are significantly decreased in activated CB versus PB MNCs, in part secondary to increased degradation of CB IL-18 mRNA. These results may have implications for the mechanism(s) in part responsible for the immaturity of CB T-cell immunity.

摘要

我们之前已经证明,活化的脐血(CB)与外周血(PB)单个核细胞(MNCs)之间存在IL-12和IL-15基因及蛋白表达失调。在本研究中,我们比较了基础状态及活化状态下CB与PB MNCs中IL-18基因表达、蛋白产生及IL-18 mRNA半衰期,IL-18 ± IL-12对MNCs IFN-γ蛋白产生的影响,以及用IL-12 + IL-2 + 抗CD3 ± IL-18对CB进行体外扩增和活化的情况。PB MNCs中IL-18的基础水平和活化水平显著高于CB MNCs(P < 0.05)。IL-18 mRNA水平与蛋白水平一致,在CB中显著较低(P < 0.05),且其半衰期在CB MNCs中比PB MNCs显著更短(P < 0.05)。IL-18与IL-12协同诱导PB MNCs产生的IFN-γ多于CB MNCs(P < 0.05)。IL-12 + IL-2 + 抗CD3和IL-18可显著增加NK细胞扩增(P < 0.001)和细胞毒性(P < 0.01)。总之,活化的CB MNCs与PB MNCs相比,IL-18基因表达和蛋白产生显著降低,部分原因是CB中IL-18 mRNA降解增加。这些结果可能对导致CB T细胞免疫不成熟的部分机制具有启示意义。

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