Abstract
Chronic hypoxia is a major contributor to tubulointerstitial injury in various renal diseases and apoptosis is apparently involved. Although many studies report hypoxia-induced apoptosis in cultured tubular cells, information has been limited in proximal tubular cells, those from the most susceptible portion of renal tubules against hypoxia. This study was to confirm a role for apoptosis in hypoxic proximal tubular cells and to investigate its association with HIF-1. Temperature-sensitive SV40-immortalized rat proximal tubular cells (IRPTCs) showed apoptosis in 21.9+/-2.9% by hypoxia (0.2% O(2), 48h), with alterations in mitochondrial signaling such as Bcl2 and caspase-9. Bax mRNA was unaffected during the process. However, treating IRPTCs at the nonpermissive temperature showed an upregulation of Bax by hypoxia, which was abrogated by overexpressing dominant-negative HIF-1alpha. These findings extend previous reports on hypoxia-mediated tubular cell apoptosis and demonstrate the possible involvement of HIF-1 as an upstream molecule of Bax.
Publication types
-
Research Support, Non-U.S. Gov't
MeSH terms
-
Animals
-
Apoptosis*
-
Blotting, Western
-
Caspase 9
-
Caspases / metabolism
-
Cell Line
-
DNA-Binding Proteins / metabolism*
-
Genes, Dominant
-
Hypoxia*
-
Hypoxia-Inducible Factor 1
-
Hypoxia-Inducible Factor 1, alpha Subunit
-
Immunoblotting
-
Immunohistochemistry
-
In Situ Nick-End Labeling
-
Kidney Tubules, Proximal / cytology*
-
Kidney Tubules, Proximal / metabolism*
-
Male
-
Membrane Potentials
-
Mitochondria / metabolism*
-
Nuclear Proteins / metabolism*
-
Oligonucleotides, Antisense / chemistry
-
Phenotype
-
Polymerase Chain Reaction
-
Proto-Oncogene Proteins / biosynthesis*
-
Proto-Oncogene Proteins c-bcl-2 / metabolism
-
RNA, Messenger / metabolism
-
Rats
-
Rats, Wistar
-
Reverse Transcriptase Polymerase Chain Reaction
-
Signal Transduction
-
Simian virus 40 / metabolism*
-
Temperature
-
Time Factors
-
Transcription Factors*
-
Transfection
-
Tumor Cells, Cultured
-
Tumor Suppressor Protein p53 / metabolism
-
Up-Regulation*
-
bcl-2-Associated X Protein
Substances
-
Bax protein, rat
-
DNA-Binding Proteins
-
Hif1a protein, rat
-
Hypoxia-Inducible Factor 1
-
Hypoxia-Inducible Factor 1, alpha Subunit
-
Nuclear Proteins
-
Oligonucleotides, Antisense
-
Proto-Oncogene Proteins
-
Proto-Oncogene Proteins c-bcl-2
-
RNA, Messenger
-
Transcription Factors
-
Tumor Suppressor Protein p53
-
bcl-2-Associated X Protein
-
Casp9 protein, rat
-
Caspase 9
-
Caspases