Erythropoietin

EPO
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesEPO, EP, MVCD2, erythropoietin, Erythropoietin, ECYT5, DBAL
External IDsOMIM: 133170; MGI: 95407; HomoloGene: 624; GeneCards: EPO; OMA:EPO - orthologs
Orthologs
SpeciesHumanMouse
Entrez

2056

13856

Ensembl

ENSG00000130427

ENSMUSG00000029711

UniProt

P01588

P07321

RefSeq (mRNA)

NM_000799

NM_007942
NM_001312875

RefSeq (protein)

NP_000790

NP_001299804
NP_031968

Location (UCSC)Chr 7: 100.72 – 100.72 MbChr 5: 137.48 – 137.53 Mb
PubMed search
Wikidata
View/Edit HumanView/Edit Mouse

Erythropoietin (/ɪˌrɪθrˈpɔɪ.ɪtɪn, -rə-, -pɔɪˈɛtɪn, -ˈtɪn/; EPO), also known as erythropoetin, haematopoietin, or haemopoietin, is a glycoprotein cytokine secreted mainly by the kidneys in response to cellular hypoxia; it stimulates red blood cell production (erythropoiesis) in the bone marrow. Low levels of EPO (around 10 mU/mL) are constantly secreted in sufficient quantities to compensate for normal red blood cell turnover. Common causes of cellular hypoxia resulting in elevated levels of EPO (up to 10 000 mU/mL) include any anemia, and hypoxemia due to chronic lung disease.

Erythropoietin is largely synthesized by fibroblast-like type-1 interstitial cells, located primarily in the deep renal cortex in close association with the peritubular capillaries and proximal convoluted tubule; it is also produced in perisinusoidal cells in the liver. Liver production predominates in the fetal and perinatal period; renal production predominates in adulthood. It is homologous with thrombopoietin.

Exogenous erythropoietin, recombinant human erythropoietin (rhEPO), is produced by recombinant DNA technology in cell culture and are collectively called erythropoiesis-stimulating agents (ESA): two examples are epoetin alfa and epoetin beta. ESAs are used in the treatment of anemia in chronic kidney disease, anemia in myelodysplasia, and in anemia from cancer chemotherapy. Risks of therapy include death, myocardial infarction, stroke, venous thromboembolism, and tumor recurrence. Risk increases when EPO treatment raises hemoglobin levels over 11 g/dL to 12 g/dL: this is to be avoided.

rhEPO has been used illicitly as a performance-enhancing drug. It can often be detected in blood, due to slight differences from the endogenous protein; for example, in features of posttranslational modification.