TY - JOUR
T1 - Cytokine induced expression of porcine inhibitor of apoptosis protein (iap) family member is regulated by NF-(κ)B
AU - Stehlik, Christian
AU - De Martin, Rainer
AU - Binder, Bernd R.
AU - Lipp, Joachim
N1 - Funding Information:
The GenBank accession number for piap is U79142. We thank Ernie Schwarzinger for her contribution of porcine aortic endothelial cells. This work was supported by grants to J.L. from the Austrian Science foundation, Project SFB 005-05, and from the Jubilaeums-fonds of the Austrian National Bank, Project 5548.
PY - 1998/2/24
Y1 - 1998/2/24
N2 - The inhibitor of apoptosis (iap) proteins belong to a gene family that protect certain cell to undergo programmed cell death in response to a variety of stimuli. By differential screening we have identified a cDNA clone, designated piap, in porcine aortic endothelial cells (PAEC) that turned out by sequence comparison to be a porcine member of the lap family, The expression of piap is strongly up-regulated upon treatment of endothelial cells (EC) with inflammatory cytokines TNF-α, IL-1β, and LPS. In EC these stimuli lead to the activation of nuclear transcription factor kappa B (NF-κB) that plays a role in countering TNF-α induced apoptosis. We demonstrate that adenovirus mediated overexpression of IκBα, an inhibitor of NF-κB suppresses the expression of piap in response to TNF-α suggesting that piap is one of the NF-κB regulated genes that operates to prevent programmed cell death of EC in inflammation.
AB - The inhibitor of apoptosis (iap) proteins belong to a gene family that protect certain cell to undergo programmed cell death in response to a variety of stimuli. By differential screening we have identified a cDNA clone, designated piap, in porcine aortic endothelial cells (PAEC) that turned out by sequence comparison to be a porcine member of the lap family, The expression of piap is strongly up-regulated upon treatment of endothelial cells (EC) with inflammatory cytokines TNF-α, IL-1β, and LPS. In EC these stimuli lead to the activation of nuclear transcription factor kappa B (NF-κB) that plays a role in countering TNF-α induced apoptosis. We demonstrate that adenovirus mediated overexpression of IκBα, an inhibitor of NF-κB suppresses the expression of piap in response to TNF-α suggesting that piap is one of the NF-κB regulated genes that operates to prevent programmed cell death of EC in inflammation.
UR - http://www.scopus.com/inward/record.url?scp=0032562085&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0032562085&partnerID=8YFLogxK
U2 - 10.1006/bbrc.1998.8185
DO - 10.1006/bbrc.1998.8185
M3 - Article
C2 - 9501011
AN - SCOPUS:0032562085
SN - 0006-291X
VL - 243
SP - 827
EP - 832
JO - Biochemical and Biophysical Research Communications
JF - Biochemical and Biophysical Research Communications
IS - 3
ER -