TY - JOUR
T1 - Interleukin-1β inhibits the hypoxic inducibility of the erythropoietin enhancer by suppressing hepatocyte nuclear factor-4α
AU - Krajewski, J.
AU - Batmunkh, C.
AU - Jelkmann, W.
AU - Hellwig-Bürgel, T.
N1 - Copyright:
Copyright 2008 Elsevier B.V., All rights reserved.
PY - 2007/4
Y1 - 2007/4
N2 - The suppression of hypoxia-induced erythropoietin (EPO) expression by inflammatory cytokines like interleukin-1 (IL-1) contributes to the development of the anemia of chronic disease (ACD). However, the precise mechanism of this suppression is unclear. The 3'-EPO enhancer mediates the transcriptional response to hypoxia by binding several transcription factors, including hypoxia-inducible factor, hepatocyte nuclear factor-4α (HNF-4α) and chicken ovalbumin upstream promoter transcription factor. We investigated whether IL-1β inhibits the activity of the 3'-EPO enhancer via HNF-4α. IL-1β inhibited HNF-4α mRNA expression and caused proteasome-dependent degradation of HNF-4α protein, which resulted in a strongly reduced DNA-binding activity of HNF-4α. Reporter gene assays revealed that IL-1β caused a complete suppression of the hypoxic inducibility of the 3′ enhancer via inhibition of HNF-4α. We conclude that IL-1β, at least partially, reduces hypoxia-induced EPO expression by down-regulation of HNF-4α.
AB - The suppression of hypoxia-induced erythropoietin (EPO) expression by inflammatory cytokines like interleukin-1 (IL-1) contributes to the development of the anemia of chronic disease (ACD). However, the precise mechanism of this suppression is unclear. The 3'-EPO enhancer mediates the transcriptional response to hypoxia by binding several transcription factors, including hypoxia-inducible factor, hepatocyte nuclear factor-4α (HNF-4α) and chicken ovalbumin upstream promoter transcription factor. We investigated whether IL-1β inhibits the activity of the 3'-EPO enhancer via HNF-4α. IL-1β inhibited HNF-4α mRNA expression and caused proteasome-dependent degradation of HNF-4α protein, which resulted in a strongly reduced DNA-binding activity of HNF-4α. Reporter gene assays revealed that IL-1β caused a complete suppression of the hypoxic inducibility of the 3′ enhancer via inhibition of HNF-4α. We conclude that IL-1β, at least partially, reduces hypoxia-induced EPO expression by down-regulation of HNF-4α.
UR - http://www.scopus.com/inward/record.url?scp=34247123177&partnerID=8YFLogxK
U2 - 10.1007/s00018-007-6561-9
DO - 10.1007/s00018-007-6561-9
M3 - Journal articles
C2 - 17372675
AN - SCOPUS:34247123177
SN - 1420-682X
VL - 64
SP - 989
EP - 998
JO - Cellular and Molecular Life Sciences
JF - Cellular and Molecular Life Sciences
IS - 7-8
ER -