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Implications for invariant natural killer T cell ligands due to the restricted presence of isoglobotrihexosylceramide in mammals

机译:由于哺乳动物体内异球三己糖基神经酰胺的存在受到限制,对自然杀伤性T细胞配体具有一定的影响

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Development of invariant natural killer T (iNKT) cells requires the presentation of lipid ligand(s) by CD1d molecules in the thymus. The glycosphingolipid (GSL) isoglobotrihexosylceramide (iGb3) has been proposed as the natural iNKT cell-selecting ligand in the thymus and to be involved in peripheral activation of iNKT cells by dendritic cells (DCs). However, there is no direct biochemical evidence for the presence of iGb3 in mouse or human thymus or DCs. Using a highly sensitive HPLC assay, the only tissue where iGb3 could be detected in mouse was the dorsal root ganglion (DRG). iGb3 was not detected in other mouse or any human tissues analyzed, including thymus and DCs. Even in mutant mice that store isoglobo-series GSLs in the DRG, we were still unable to detect these GSLs in the thymus. iGb3 is therefore unlikely to be a physiologically relevant iNKT cell-selecting ligand in mouse and humans. A detailed study is now warranted to better understand the nature of iNKT cell-selecting ligand(s) in vivo.
机译:不变的自然杀伤T细胞(iNKT)的发展需要胸腺中CD1d分子呈递脂质配体。糖鞘脂(GSL)异球三己糖基神经酰胺(iGb3)已被提出作为胸腺中的天然iNKT细胞选择配体,并参与树突状细胞(DC)对iNKT细胞的外周活化。但是,没有直接的生化证据表明在小鼠或人的胸腺或DC中存在iGb3。使用高灵敏度的HPLC分析,可以在小鼠中检测到iGb3的唯一组织是背根神经节(DRG)。在其他小鼠或分析的任何人体组织(包括胸腺和DC)中均未检测到iGb3。即使是在DRG中存储了等球蛋白系列GSL的突变小鼠中,我们仍然无法在胸腺中检测到这些GSL。因此,iGb3在小鼠和人类中不太可能是生理相关的iNKT细胞选择配体。现在有必要进行详细的研究,以更好地了解体内iNKT细胞选择配体的性质。

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