摘要：SummaryIn the finely regulated process of mammalian erythropoiesis, the path of the labile iron pool into mitochondria for heme production is not well understood. Existing models for erythropoiesis do not include a central role for the ubiquitous iron storage protein ferritin; one model proposes that incoming endosomal Fe3+bound to transferrin enters the cytoplasm through an ion transporter after reduction to Fe2+and is taken up into mitochondria through mitoferrin-1 transporter. Here, we apply a dual three-dimensional imaging and spectroscopic technique, based on scanned electron probes, to measure Fe3+inex vivohuman hematopoietic stem cells. After seven days in culture, we observe cells displaying a highly specialized architecture with anchored clustering of mitochondria and massive accumulation of nanoparticles containing high iron concentrations localized to lysosomal storage depots, identified as ferritin. We hypothesize that lysosomal ferritin iron depots enable continued heme production after expulsion of most of the cellular machinery.Graphical abstractDisplay OmittedHighlights•Erythroblasts maintain highly organized architecture as revealed by SB-SEM•STEM/EELS reveal ferritin-containing lysosomal vesicles surrounded by mitochondria•In erythropoiesis, ferritin is attributed to be an iron depot used in heme synthesisBiological sciences; Biochemistry; Cell biology; Technical aspects of cell biology
