Abstract
Erythropoietin (EPO) is a 165 amino acid glycoprotein hormone (30.4 kDa) member of the type 1 cytokine superfamily that is produced primarily by renal cortical and outer medullary type 1 fibroblasts [1] in response to tissue hypoxia under the control of the oxygen-sensitive transcription factor hypoxia-inducible factor-l (HIF-l). EPO binds to a preformed EPO receptor homodimer (EPOR)2 present on the cell membrane of erythrocyte progenitors. On activation of (EPOR)2 a molecular cascade begins with the phosphorylation of Janus tyrosine kinase 2, which ultimately results in inhibition of programmed cell death, principally involving Akt and the Bcl-2 gene family, resulting in the survival and maturation of erythroid progenitor cells to erythrocytes [2]. The overall effect is a compensatory adaptation to tissue hypoxia by enhancing the oxygen-carrying capacity of the blood [3], and thus may be therapeutically useful for the treatment of anemia associated with chronic kidney disease or chemotherapy [4–6].
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Patel, N.S.A., Yaqoob, M.M., Thiemermann, C. (2010). Tissue Protective Activities of Erythropoietin. In: Vincent, JL. (eds) Intensive Care Medicine. Springer, New York, NY. https://doi.org/10.1007/978-1-4419-5562-3_30
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DOI: https://doi.org/10.1007/978-1-4419-5562-3_30
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