Regulation of heavy subunit chain of γ-glutamylcysteine synthetase by tumor necrosis factor-α in lens epithelial cells: Role of LEDGF/p75

Yoshihiro Takamura, Nigar Fatma, Eri Kubo, Dhirendra P. Singh

Research output: Contribution to journalArticle

22 Citations (Scopus)

Abstract

TNF-α induces oxidative stress by generating reactive oxygen species (ROS). This molecule elevates the expression of γ-glutamylcysteine synthetase heavy subunit (γ-GCSHS). Lens epithelium-derived growth factor (LEDGF)/p75, a transcriptional protein, is inducible by oxidative stress and protects cells from various stresses by upregulating stress-responsive genes. This paper presents evidence that TNF-α elevates the expression of LEDGF and that LEDGF is one of the transactivators of γ-GCS-HS gene. An analysis of the γ-GCS-HS promoter sequence (-819 to +518 nt) revealed the presence of putative sites for LEDGF binding. Gel mobility assay confirmed the binding of LEDGF to the heat shock element (nGAAn) and the stress response element (A/TGGGGA/T) present in γ-GCS-HS promoter. Transactivation experiments showed activation of γ-GCS-HS promoter in cells overexpressing LEDGF or treated with a sublethal dose of TNF-α (20 ng/ml). Downregulation of γ-GCS-HS promoter activity in cells transfected with LEDGF small interfering RNA validated the finding. Notably, cells treated with TNF-α (20 ng/ml) for 24 h had an increased abundance of LEDGF and γ-GCS-HS mRNA and protein. In contrast, cells treated with TNF-α for longer periods or with higher concentrations of TNF-α showed reduced expression of LEDGF and γ-GCS-HS and increased cellular death with higher ROS levels. Cells overexpressing LEDGF revealed elevated GSH levels (10-15%), a condition that may potentially eliminate the insult to cells induced by TNF-α. Thus TNF-α regulation of LEDGF may be physiologically important, as elevated expression of LEDGF increases the expression of endogenous γ-GCS-HS gene, the catalytic subunit of the regulating enzyme in GSH biosynthesis that may constitute a protective mechanism in limiting oxidative stress induced by inflammatory cytokines.

Original languageEnglish (US)
Pages (from-to)C554-C566
JournalAmerican Journal of Physiology - Cell Physiology
Volume290
Issue number2
DOIs
StatePublished - Feb 1 2006

Fingerprint

Glutamate-Cysteine Ligase
Lenses
Tumor Necrosis Factor-alpha
Epithelial Cells
Oxidative stress
Oxidative Stress
Genes
lens epithelium-derived growth factor
Reactive Oxygen Species
Trans-Activators
Biosynthesis
Response Elements
Small Interfering RNA
Transcriptional Activation
Shock
Assays
Catalytic Domain

Keywords

  • Apoptosis
  • Glutathione
  • Lens epithelium-derived growth factor
  • Oxidative stress
  • Reactive oxygen species

ASJC Scopus subject areas

  • Physiology
  • Cell Biology

Cite this

Regulation of heavy subunit chain of γ-glutamylcysteine synthetase by tumor necrosis factor-α in lens epithelial cells : Role of LEDGF/p75. / Takamura, Yoshihiro; Fatma, Nigar; Kubo, Eri; Singh, Dhirendra P.

In: American Journal of Physiology - Cell Physiology, Vol. 290, No. 2, 01.02.2006, p. C554-C566.

Research output: Contribution to journalArticle

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abstract = "TNF-α induces oxidative stress by generating reactive oxygen species (ROS). This molecule elevates the expression of γ-glutamylcysteine synthetase heavy subunit (γ-GCSHS). Lens epithelium-derived growth factor (LEDGF)/p75, a transcriptional protein, is inducible by oxidative stress and protects cells from various stresses by upregulating stress-responsive genes. This paper presents evidence that TNF-α elevates the expression of LEDGF and that LEDGF is one of the transactivators of γ-GCS-HS gene. An analysis of the γ-GCS-HS promoter sequence (-819 to +518 nt) revealed the presence of putative sites for LEDGF binding. Gel mobility assay confirmed the binding of LEDGF to the heat shock element (nGAAn) and the stress response element (A/TGGGGA/T) present in γ-GCS-HS promoter. Transactivation experiments showed activation of γ-GCS-HS promoter in cells overexpressing LEDGF or treated with a sublethal dose of TNF-α (20 ng/ml). Downregulation of γ-GCS-HS promoter activity in cells transfected with LEDGF small interfering RNA validated the finding. Notably, cells treated with TNF-α (20 ng/ml) for 24 h had an increased abundance of LEDGF and γ-GCS-HS mRNA and protein. In contrast, cells treated with TNF-α for longer periods or with higher concentrations of TNF-α showed reduced expression of LEDGF and γ-GCS-HS and increased cellular death with higher ROS levels. Cells overexpressing LEDGF revealed elevated GSH levels (10-15{\%}), a condition that may potentially eliminate the insult to cells induced by TNF-α. Thus TNF-α regulation of LEDGF may be physiologically important, as elevated expression of LEDGF increases the expression of endogenous γ-GCS-HS gene, the catalytic subunit of the regulating enzyme in GSH biosynthesis that may constitute a protective mechanism in limiting oxidative stress induced by inflammatory cytokines.",
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