Why is a mature rbc biconcave
Enucleation involves dramatic chromatin condensation and establishment of the nuclear polarity, which is driven by a rearrangement of actin cytoskeleton and the clathrin-dependent generation of vacuoles at the nuclear-cytoplasmic junction. This process is favored by interaction between the erythroblasts and macrophages at the erythroblastic island.
Mitochondria are eliminated by mitophagy. Human erythrocytes or red blood cells RBCs are the primary cellular component of blood. They are involved in oxygen transport through the body and have features that distinguish them from every other type of human cell. Adult humans have roughly trillion RBCs at any given time, comprising approximately one quarter of the total number of human cells. RBCs are disc-shaped with a flatter, concave center.
This biconcave shape allows the cells to flow smoothly through the narrowest blood vessels. Gas exchange with tissues occurs in capillaries, tiny blood vessels that are only as wide as one cell. Many RBCs are wider than capillaries, but their shape provides the needed flexibility to squeeze through. Carayon, K. Proteolipidic composition of exosomes changes during reticulocyte maturation. Chan, E. Chen, Z. Autophagy 13, — Da Costa, L.
Temporal differences in membrane loss lead to distinct reticulocyte features in hereditary spherocytosis and in immune hemolytic anemia. Blood 98, — Of macrophages and red blood cells; a complex love story. De Franceschi, L. Pathophisiology of sickle cell disease and new drugs for the treatment. Dellagi, K. Alteration of vimentin intermediate filament expression during differentiation of human hemopoietic cells. EMBO J. PubMed Abstract Google Scholar. Fader, C. Hemin induces mitophagy in a leukemic erythroblast cell line: hemin induces mitophagy in K cells.
Cell , 77— Franco, S. Resveratrol accelerates erythroid maturation by activation of FoxO3 and ameliorates anemia in beta-thalassemic mice. Haematologica 99, — Garderet, L. Unimpaired terminal erythroid differentiation and preserved enucleation capacity in myelodysplastic 5q del clones: a single cell study.
Haematologica 95, — Geisler, S. Cell Biol. Gnanapragasam, M. Gothwal, M. A novel role for nuclear factor-erythroid 2 in erythroid maturation by modulation of mitochondrial autophagy. Haematologica , — Griffiths, R.
Maturing reticulocytes internalize plasma membrane in glycophorin A-containing vesicles that fuse with autophagosomes before exocytosis. Inhibition of lipoxygenase leads to delayed organelle degradation in the reticulocyte. FEBS Lett. Hamasaki, M. Autophagosomes form at ER—mitochondria contact sites. Nature , — Hammerling, B. A Rab5 endosomal pathway mediates Parkin-dependent mitochondrial clearance. Small GTPases 11, 1—8. Holroyde, C.
Acquisition of autophagic vacuoles by human erythrocytes physiological role of the spleen. Blood 36, — Honda, S. Ulk1-mediated Atg5-independent macroautophagy mediates elimination of mitochondria from embryonic reticulocytes. Hung, Y.
Spatiotemporally controlled induction of autophagy-mediated lysosome turnover. Iwata, J. Excess peroxisomes are degraded by autophagic machinery in mammals. Jagadeeswaran, R. Jayapal, S. Down-regulation of Myc is essential for terminal erythroid maturation. Ji, P. Histone deacetylase 2 is required for chromatin condensation and subsequent enucleation of cultured mouse fetal erythroblasts.
Ji, Y. EPO improves the proliferation and inhibits apoptosis of trophoblast and decidual stromal cells through activating STAT-5 and inactivating p38 signal in human early pregnancy. Johnstone, R. Vesicle formation during reticulocyte maturation. Association of plasma membrane activities with released vesicles exosomes. Reticulocyte maturation and exosome release: transferrin receptor containing exosomes shows multiple plasma membrane functions.
Blood 19, — Google Scholar. Keerthivasan, G. A novel role for survivin in erythroblast enucleation. Haematologica 97, — Vesicle trafficking plays a novel role in erythroblast enucleation. Khandros, E. Killisch, I. Characterization of early and late endocytic compartments of the transferrin cycle. Transferrin receptor antibody blocks erythroid differentiation by trapping the receptor in the early endosome.
Cell Sci. Kim, Y. PINK1 controls mitochondrial localization of Parkin through direct phosphorylation. Kobayashi, I.
Erythroblast enucleation is a dynein-dependent process. Koury, S. Cytoskeletal distribution and function during the maturation and enucleation of 13 mammalian erythroblasts. Koury, M. In vitro maturation of nascent reticulocytes to erythrocytes. Each chain has a heme group that contains an iron atom. Oxygen can bind to these iron atoms, which means that one molecule of hemoglobin can carry four oxygen molecules.
In the lungs, the hemoglobin in the red blood cells picks up oxygen. However, hemoglobin does not carry all the carbon dioxide in the blood back to the lungs—the blood can also transport CO2 as a dissolved gas or as bicarbonate HCO3. Like red blood cells, platelets are derived from myeloid stem cells. Some of these stem cells develop into megakaryoblasts, which give rise to cells called megakaryocytes in the bone marrow.
After a megakaryocyte has matured, pieces of its cytoplasm break away into cell fragments called platelets. A single megakaryocyte can produce — platelets. However, they do contain numerous granules or vesicles.
The hormone thrombopoietin, produced by the liver and kidneys, regulates the production of megakaryocytes and platelets. Platelets have different appearances in their inactivated and activated states.
When inactivated , platelets are irregularly shaped discs. Activated platelets are spherical, with protrusions that allow them to stick to wound tissue and to other platelets to form a plug at the site of a blood vessel tear.
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