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Oxygen availability regulates metabolism and gene expression in trout hepatocyte cultures




TekijätRissanen E, Tranberg HK, Nikinmaa M

KustantajaAMER PHYSIOLOGICAL SOC

Julkaisuvuosi2006

JournalAJP - Regulatory, Integrative and Comparative Physiology

Tietokannassa oleva lehden nimiAMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY

Lehden akronyymiAM J PHYSIOL-REG I

Vuosikerta291

Numero5

AloitussivuR1507

LopetussivuR1515

Sivujen määrä9

ISSN0363-6119

DOIhttps://doi.org/10.1152/ajpregu.00025.2006


Tiivistelmä

Oxygen availability regulates metabolism and gene expression in trout hepatocyte cultures. AmJ Physiol Regul Integr Comp Physiol 291: R1507-R1515, 2006. First published June 15, 2006; doi: 10.1152/ajpregu.00025.2006.-We studied the metabolic rate, cellular energetic state, hypoxia-inducible factor-1 (HIF-1) activation, and expression of enzymes involved in energy metabolism using rainbow trout (Oncorhynchus mykiss) hepatocytes over the oxygen range from 21 to 1 kPa. Oxygen dependence of these factors was assessed by gradually reducing oxygen supply to cells from 21 kPa to 10, 5, 2, and 1 kPa. Moreover, time course experiments for up to 20 h at oxygen tensions of 1 and 2 kPa were carried out. Reduction of oxygen from 21 kPa to 10, 5, 2, and 1 kPa decreased metabolic rate of the cells by 14, 24, 37, and 46%, respectively. This response was instantaneous and fully reversible upon reoxygenation. Cellular ATP content and the expression of all mRNAs studied decreased when oxygen was reduced from 21 to 5 and 2 kPa. The lowest ATP levels, similar to 43% of the initial value, were measured at 5 kPa of oxygen, whereas the reduction in mRNA amounts was most pronounced at 2 kPa. At 1 kPa oxygen tension, both ATP content and mRNA amounts returned to normoxic (21 kPa) levels with a concomitant activation of HIF-1, indicating reorganization of energy metabolism in adaptation of cells to low oxygen supply. These results show that oxygen has a direct regulatory effect on metabolism of trout hepatocyte cultures, supporting the view that oxygen has a profound role in metabolic regulation in cells.




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