National Institute of Gastroenterology "S. de Bellis", Research Hospital, Castellana Grotte, 70013 Bari, Italy.
Department of Immunology and Cell Biology, European Biomedical Research Institute of Salerno (EBRIS), 84125 Salerno, Italy.
Int J Mol Sci. 2020 Feb 17;21(4):1353. doi: 10.3390/ijms21041353.
Iron overload is an undesired effect of frequent blood transfusions or genetic diseases. Myelodysplastic syndrome (MDS) patients become transfusion dependent, but due to the combination of ineffective haematopoiesis and repeated blood transfusions they are often subject to iron overload. In this study, we demonstrate that iron-overload mimicking condition alters bone marrow progenitor differentiation towards dendritic cells (DCs). Cells cultured in iron-enriched culture medium for seven days fail to differentiate into conventional CD11cMHCII DCs and fail to efficiently respond to LPS (Lipopolysaccharides). Cells appear smaller than control DCs but vital and able to perform FITC-dextran (Fluorescein isothiocyanate-dextran) endocytosis. At molecular level, cells cultured in iron-enriched conditions show increased and , and decreased expression.
铁过载是频繁输血或遗传疾病的一种不良后果。骨髓增生异常综合征 (MDS) 患者需要输血,但由于无效造血和反复输血的结合,他们经常受到铁过载的影响。在这项研究中,我们证明了铁过载模拟条件会改变骨髓祖细胞向树突状细胞 (DC) 的分化。在富含铁的培养基中培养七天的细胞不能分化为常规的 CD11cMHCII DC,也不能有效地对 LPS(脂多糖)作出反应。这些细胞比对照 DC 小,但仍具有活力,能够进行 FITC-葡聚糖(异硫氰酸荧光素-葡聚糖)内吞作用。在分子水平上,在富含铁的条件下培养的细胞显示出增加的 和 ,以及减少的 表达。