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lüll Regulated oxygen sensing by protein hydroxylation in renal erythropoietin-producing cells Wenger RH; Hoogewijs DAm J Physiol Renal Physiol 2010[Jun]; 298 (6): F1287-96The kidney is a major site of systemic oxygen sensing, regulating blood erythrocyte and hence oxygen content by hypoxia-inducible erythropoietin (Epo) expression. A constant ratio between blood perfusion and oxygen consumption, a stable corticomedullary oxygen gradient, and a relatively low tissue Po(2) are the prerequisites for the function of renal Epo-producing and oxygen-sensing (REPOS) cells, which are located in the juxtamedullary cortex. In kidney disease, renal oxygen consumption is decreased, leading to an increase in Po(2), dysfunction of REPOS cells, and anemia. The molecular principles of cellular oxygen sensing have been elucidated in the last few years, and genetically altered mouse models as well as hereditary diseases causing erythrocytosis have clarified the oxygen-signaling cascade leading to increased Epo expression in REPOS cells. However, the consequences of a number of recently discovered factors for the regulation of oxygen signaling in REPOS cells are unclear, asking for novel cell culture models which might be hampered by the putative neuron-like nature of this enigmatic cell type.|Anemia/drug therapy/*etiology/genetics/metabolism/pathology[MESH]|Animals[MESH]|Basic Helix-Loop-Helix Transcription Factors/metabolism[MESH]|Erythropoietin/blood/genetics/*metabolism/therapeutic use[MESH]|Feedback, Physiological[MESH]|Gene Expression Regulation[MESH]|Hematinics/therapeutic use[MESH]|Humans[MESH]|Hydroxylation[MESH]|Hypoxia-Inducible Factor 1, alpha Subunit/metabolism[MESH]|Hypoxia-Inducible Factor-Proline Dioxygenases[MESH]|Kidney Diseases/complications/drug therapy/genetics/*metabolism/pathology[MESH]|Kidney/blood supply/*metabolism/pathology[MESH]|Oxygen Consumption[MESH]|Oxygen/blood/*metabolism[MESH]|Polycythemia/metabolism/pathology[MESH]|Procollagen-Proline Dioxygenase/metabolism[MESH]|Renal Circulation[MESH]|Signal Transduction[MESH]|Von Hippel-Lindau Tumor Suppressor Protein/metabolism[MESH] |