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Kurtz, Armin ; Jelkmann, W. ; Pfuhl, A. ; Malmström, K. ; Bauer, Christian

Erythropoietin production by fetal mouse liver cells in response to hypoxia and adenylate cyclase stimulation

Kurtz, Armin, Jelkmann, W., Pfuhl, A., Malmström, K. und Bauer, Christian (1986) Erythropoietin production by fetal mouse liver cells in response to hypoxia and adenylate cyclase stimulation. Endocrinology 118 (2), S. 567-572.

Veröffentlichungsdatum dieses Volltextes: 08 Jan 2013 08:09
Artikel
DOI zum Zitieren dieses Dokuments: 10.5283/epub.27010


Zusammenfassung

This study was done to investigate aspects of control of extrarenal erythropoietin (Ep) production. To this end we studied the effects of three stimuli of renal Ep production in the adult, i.e. hypoxia, cobalt, and activation of adenylate cyclase on Ep generation by cultured fetal mouse liver cells. The fetal liver was taken as a model for extrarenal Ep production because this organ is considered ...

This study was done to investigate aspects of control of extrarenal erythropoietin (Ep) production. To this end we studied the effects of three stimuli of renal Ep production in the adult, i.e. hypoxia, cobalt, and activation of adenylate cyclase on Ep generation by cultured fetal mouse liver cells. The fetal liver was taken as a model for extrarenal Ep production because this organ is considered the predominant site of extrarenal Ep production. We found that Ep production by the cells increased as the oxygen concentration was decreased in the incubation atmosphere from 20% to 1%. Cobalt (10(-4)-10(-5) M) had no effect on Ep production. Activation of adenylate cyclase by forskolin (10(-5) M) or isoproterenol (10(-5) M) greatly enhanced Ep production. These findings indicate that the Ep-stimulating effect of cobalt is specific for the kidney. However, oxygen depletion and activation of adenylate cyclase seem to be more general stimuli in Ep-producing cells. Furthermore we found that Ep production in hypoxia correlated with lactate formation in the cultured liver cells. This finding suggests that Ep production in fetal livers under hypoxic conditions parallels the shift from aerobic to anaerobic cellular energy metabolism.



Beteiligte Einrichtungen


Details

DokumentenartArtikel
Titel eines Journals oder einer ZeitschriftEndocrinology
Verlag:Endocrine Society
Band:118
Nummer des Zeitschriftenheftes oder des Kapitels:2
Seitenbereich:S. 567-572
Datum1986
InstitutionenBiologie und Vorklinische Medizin > Institut für Physiologie > Prof. Dr. Armin Kurtz
Identifikationsnummer
WertTyp
3002755PubMed-ID
Klassifikation
NotationArt
Adenylate Cyclase/metabolismMESH
AnimalsMESH
Cells, CulturedMESH
Cobalt/pharmacologyMESH
Cyclic AMP/metabolismMESH
Enzyme Activation/drug effectsMESH
Erythropoietin/biosynthesisMESH
Forskolin/pharmacologyMESH
Isoproterenol/pharmacologyMESH
KineticsMESH
Lactates/biosynthesisMESH
Lactic AcidMESH
Liver/metabolismMESH
MiceMESH
Oxygen/pharmacologyMESH
Dewey-Dezimal-Klassifikation500 Naturwissenschaften und Mathematik > 570 Biowissenschaften, Biologie
600 Technik, Medizin, angewandte Wissenschaften > 610 Medizin
StatusVeröffentlicht
BegutachtetJa, diese Version wurde begutachtet
An der Universität Regensburg entstandenUnbekannt / Keine Angabe
URN der UB Regensburgurn:nbn:de:bvb:355-epub-270105
Dokumenten-ID27010

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