Lund Stem Cell Center, Division of Molecular Hematology, Lund University, 221 84 Lund, Sweden.
Department of Clinical Sciences, Division of Infection Medicine, Lund University, 221 84 Lund, Sweden.
Cell Rep. 2017 Dec 12;21(11):3285-3297. doi: 10.1016/j.celrep.2017.11.070.
Hematopoietic stem and progenitor cells (HSPCs) in the fetus and adult possess distinct molecular landscapes that regulate cell fate and change their susceptibility to initiation and progression of hematopoietic malignancies. Here, we applied in-depth quantitative proteomics to comprehensively describe and compare the proteome of fetal and adult HSPCs. Our data uncover a striking difference in complexity of the cellular proteomes, with more diverse adult-specific HSPC proteomic signatures. The differential protein content in fetal and adult HSPCs indicate distinct metabolic profiles and protein complex stoichiometries. Additionally, adult characteristics include an arsenal of proteins linked to viral and bacterial defense, as well as protection against ROS-induced protein oxidation. Further analyses show that interferon α, as well as Neutrophil elastase, has distinct functional effects in fetal and adult HSPCs. This study provides a rich resource aimed toward an enhanced mechanistic understanding of normal and malignant hematopoiesis during fetal and adult life.
胎儿和成人造血干细胞和祖细胞 (HSPCs) 具有不同的分子特征,这些特征调节着细胞命运,并改变它们对造血恶性肿瘤起始和进展的易感性。在这里,我们应用深度定量蛋白质组学来全面描述和比较胎儿和成人 HSPC 的蛋白质组。我们的数据揭示了细胞蛋白质组复杂性的惊人差异,具有更多样化的成人特异性 HSPC 蛋白质组特征。胎儿和成人 HSPC 中差异蛋白的含量表明存在不同的代谢特征和蛋白质复合物化学计量。此外,成人特征包括与病毒和细菌防御以及抵抗 ROS 诱导的蛋白质氧化相关的一系列蛋白质。进一步的分析表明,干扰素 α 以及中性粒细胞弹性蛋白酶在胎儿和成人 HSPC 中具有不同的功能作用。这项研究提供了一个丰富的资源,旨在增强对胎儿和成人生命中正常和恶性造血的机制理解。