4.3 Article

Increased prolyl 4-hydroxylase expression and differential regulation of hypoxia-inducible factors in the aged rat brain

Publisher

AMER PHYSIOLOGICAL SOC
DOI: 10.1152/ajpregu.90829.2008

Keywords

aging; hypoxia; hypoxia inducible factor-1; hypoxia inducible factor-2

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Funding

  1. National Institutes of Health [R01-NS38632, T32-GM007250]

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Ndubuizu OI, Chavez JC, LaManna JC. Increased prolyl 4-hydroxylase expression and differential regulation of hypoxia-inducible factors in the aged rat brain. Am J Physiol Regul Integr Comp Physiol 297: R158-R165, 2009. First published May 6, 2009; doi:10.1152/ajpregu.90829.2008.-Hypoxia-inducible factors (HIFs) are heterodimeric transcription factors that mediate the adaptive response of mammalian cells and tissues to changes in tissue oxygenation. In the present study, we show an age-dependent decline in cortical HIF-1 alpha accumulation and activation of HIF target genes in response to hypoxia. This inducible response is significantly attenuated in the cerebral cortex of 18-mo-old Fischer 344 rat yet virtually absent in the cerebral cortex of 24-mo-old Fischer 344 rat. This attenuated HIF-1 alpha response had no effect on mRNA upregulation of HIF-independent genes in the aged cortex. We have provided evidence that this absent HIF-1 alpha response is directly correlated with an increase in the expression of the HIF regulatory enzyme, prolyl 4-hydroxylase (PHD). In addition, our study shows that cortical HIF-2 alpha expression in senescent normoxic controls is also significantly greater than that of younger normoxic controls, despite no difference in HIF-2 alpha mRNA levels. The posttranslational regulation of HIF-2 alpha under normoxic conditions seems to be attenuated in the aged rat brain, which is an in vivo demonstration of differential regulation of HIF-1 alpha and HIF-2 alpha.

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