The impact of α-Lipoic acid on cell viability and expression of nephrin and ZNF580 in normal human podocytes

Eur J Pharmacol. 2017 Sep 5:810:1-8. doi: 10.1016/j.ejphar.2017.06.013. Epub 2017 Jun 10.

Abstract

Human podocytes (hPC) are essential for maintaining normal kidney function and dysfunction or loss of hPC play a pivotal role in the manifestation and progression of chronic kidney diseases including diabetic nephropathy. Previously, α-Lipoic acid (α-LA), a licensed drug for treatment of diabetic neuropathy, was shown to exhibit protective effects on diabetic nephropathy in vivo. However, the effect of α-LA on hPC under non-diabetic conditions is unknown. Therefore, we analyzed the impact of α-LA on cell viability and expression of nephrin and zinc finger protein 580 (ZNF580) in normal hPC in vitro. Protein analyses were done via Western blot techniques. Cell viability was determined using a functional assay. hPC viability was dynamically modulated via α-LA stimulation in a concentration-dependent manner. This was associated with reduced nephrin and ZNF580 expression and increased nephrin phosphorylation in normal hPC. Moreover, α-LA reduced nephrin and ZNF580 protein expression via 'kappa-light-chain-enhancer' of activated B-cells (NF-κB) inhibition. These data demonstrate that low α-LA had no negative influence on hPC viability, whereas, high α-LA concentrations induced cytotoxic effects on normal hPC and reduced nephrin and ZNF580 expression via NF-κB inhibition. These data provide first novel information about potential cytotoxic effects of α-LA on hPC under non-diabetic conditions.

Keywords: Human podocytes; Nephrin; ZNF580; α-lipoic acid.

MeSH terms

  • Cell Survival / drug effects*
  • Dose-Response Relationship, Drug
  • Gene Expression Regulation / drug effects*
  • Humans
  • Membrane Proteins / genetics
  • Membrane Proteins / metabolism*
  • Podocytes / cytology
  • Podocytes / drug effects*
  • Podocytes / metabolism*
  • Proto-Oncogene Proteins c-akt / metabolism
  • Thioctic Acid / pharmacology*
  • Transcription Factor RelA / metabolism
  • Transcription Factors / genetics
  • Transcription Factors / metabolism*

Substances

  • Membrane Proteins
  • RELA protein, human
  • Transcription Factor RelA
  • Transcription Factors
  • ZNF580 protein, human
  • nephrin
  • Thioctic Acid
  • Proto-Oncogene Proteins c-akt