Synergistic effect of hypoxia and TNF-α on production of PAI-1 in human proximal renal tubular cells

• Published in: Kidney international Vol. 68; no. 2; pp. 569 - 583
• Main Authors: Li, Xuan, Kimura, Hideki, Hirota, Kiichi, Kasuno, Kenji, Torii, Kunio, Okada, Toshiharu, Kurooka, Hisanori, Yokota, Yoshifumi, Yoshida, Haruyoshi
• Format: Journal Article
• Language: English
• Published: New York, NY Elsevier Inc 01.08.2005; Nature Publishing
• Subjects: Antineoplastic Agents - pharmacology; Biological and medical sciences; cDNA array; Cell Nucleus - metabolism; Cell Survival - drug effects; Cells, Cultured; Drug Synergism; Gene Expression Regulation; Genistein - pharmacology; HIF-1; human proximal tubular cells; Humans; hypoxia; Hypoxia - metabolism; Hypoxia-Inducible Factor 1, alpha Subunit; Kidney Tubules, Proximal - cytology; Kidney Tubules, Proximal - drug effects; Kidney Tubules, Proximal - metabolism; Medical sciences; Nephrology. Urinary tract diseases; NF-kappa B - antagonists & inhibitors; Oxygen - pharmacology; PAI-1; Plasminogen Activator Inhibitor 1 - genetics; Plasminogen Activator Inhibitor 1 - metabolism; Proline - analogs & derivatives; Proline - pharmacology; Promoter Regions, Genetic - physiology; Protein-Tyrosine Kinases - antagonists & inhibitors; Signal Transduction - drug effects; synergistic effect; Thiocarbamates - pharmacology; TNF-α; Transcription Factors - metabolism; Tumor Necrosis Factor-alpha - genetics; Tumor Necrosis Factor-alpha - pharmacology; hypoxia; HIF-1; cDNA array; TNF-α; PAI-1; human proximal tubular cells; synergistic effect; Proximal; Nephrology; Biosynthesis; Synergism; Kidney; Urology; Plasminogen activator inhibitor 1; Gene; Production; Drug interaction; Cell; Tumor necrosis factor α; Human; Oxygen; Cytokine; Tubular; Renal tubule; Urinary system; Complementary DNA; Hypoxia; Transcription factor HIF1
• ISSN: 0085-2538; 1523-1755
• DOI: 10.1111/j.1523-1755.2005.00435.x

Synergistic effect of hypoxia and TNF-α on production of PAI-1 in human proximal renal tubular cells. Chronic hypoxia has been newly proposed as a common mechanism of tubulointerstitial fibrosis in the progression of various chronic inflammatory renal diseases, where plasminogen activator inhibitor-1 (PAI-1) plays an important role in the accumulation of extracellular matrix (ECM) through inhibition of plasmin-dependent ECM degradation. In the present study, we investigated the presence of PAI-1 in renal tubular cells by immunostaining renal biopsy samples. We also closely examined the effects of hypoxia and tumor necrosis factor-α (TNF-α) on PAI-1 expression in cultured human proximal renal tubular cells (HPTECs). Confluent cells growth-arrested in Dulbecco's modified Eagle's medium (DMEM) for 24 hours were exposed to hypoxia (1% O2) and/or TNF-α at 10ng/mL for up to 48 hours. Amounts of PAI-1 protein and mRNA after stimulation were measured by enzyme-linked immunosorbent assay (ELISA) and TaqMan quantitative polymerase chain reaction (PCR) or cDNA array analysis, respectively, and compared to those in cells incubated under control conditions (18% O2 without TNF-α). Hypoxia-inducible factor-1α (HIF-1α) was demonstrated by immunoblot and immunofluorescence analyses. Human PAI-1 promoter activity was estimated by luciferase reporter gene assay. In crescentic glomerulonephritis, clusters of proximal tubules were specifically stained for PAI-1. cDNA array analysis identified PAI-1 as a major gene highly induced by hypoxia in HPTECs. Treatment of 24 hours with hypoxia, TNF-α, and their combination induced a 2.8-fold, a 1.8-fold, and a 4.6-fold increase in PAI-1 protein secretion, and produced a 3.6-fold, a 3.3-fold, and a 12.1-fold increase at the PAI-1 mRNA level, respectively. Immunoblot analysis and immunocytochemistry revealed that hypoxia-inducible factor-1α (HIF-1α) was markedly accumulated in the cell lysates and exclusively translocated to nuclei after 16 hours' exposure of HPTECs to hypoxia but not to TNF-α. Luciferase reporter gene assay showed that hypoxia, TNF-α, and their combination increased PAI-1 transcription activity by 1.8-fold, 1.4-fold, and 2.2-fold, respectively. A dominant-negative form of HIF-1α significantly suppressed PAI-1 transcription activity induced by hypoxia. Inhibition of nuclear factor-κB (NF-κB) caused a moderate decrease in PAI-1 production under hypoxia. Hypoxia induces PAI-1 expression via remarkable nuclear accumulation of HIF-1α and partially via NF-κB activation in HPTECs. TNF-α can synergistically enhance this hypoxia-induced PAI-1 expression.