RIP140/PGC-1α axis involved in vitamin A-induced neural differentiation by increasing mitochondrial function

Artif Cells Nanomed Biotechnol. 2018;46(sup1):806-816. doi: 10.1080/21691401.2018.1436552. Epub 2018 Mar 7.

Abstract

Vitamin A deficiency and mitochondrial dysfunction are both associated with neural differentiation-related disorders, such as Alzheimer's disease (AD) and Down syndrome (DS). The mechanism of vitamin A-induced neural differentiation and the notion that vitamin A can regulate the morphology and function of mitochondria in its induction of neural differentiation through the RIP140/PGC-1α axis are unclear. The aim of this study was to investigate the roles and underlying mechanisms of RIP140/PGC-1α axis in vitamin A-induced neural differentiation. Human neuroblastoma cells (SH-SY5Y) were used as a model of neural stem cells, which were incubated with DMSO, 9-cis-retinoic acid (9-cis-RA), 13-cis-retinoic acid (13-cis-RA) and all-trans-retinoic acid (at-RA). Neural differentiation of SH-SY5Y was evaluated by Sandquist calculation, combined with immunofluorescence and real-time polymerase chain reaction (PCR) of neural markers. Mitochondrial function was estimated by ultrastructure assay using transmission electron microscopy (TEM) combined with the expression of PGC-1α and NEMGs using real-time PCR. The participation of the RA signaling pathway was demonstrated by adding RA receptor antagonists. Vitamin A derivatives are able to regulate mitochondrial morphology and function, and furthermore to induce neural differentiation through the RA signaling pathway. The RIP140/PGC-1α axis is involved in the regulation of mitochondrial function in vitamin A derivative-induced neural differentiation.

Keywords: Vitamin A deficiency; mitochondrial dysfunction; neural differentiation; nuclear-encoded mitochondrial genes (NEMGs); peroxisome proliferator-activated receptor-γ co-activator 1-α (PGC-1α); receptor-interacting protein-140; retinoic acid; retinoic acid receptors.

MeSH terms

  • Cell Differentiation / drug effects*
  • Cell Line, Tumor
  • Humans
  • Mitochondria / drug effects*
  • Mitochondria / metabolism
  • Neurons / cytology*
  • Neurons / drug effects
  • Neurons / metabolism
  • Nuclear Receptor Interacting Protein 1 / metabolism*
  • Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha / metabolism*
  • Vitamin A / analogs & derivatives
  • Vitamin A / pharmacology*

Substances

  • Nuclear Receptor Interacting Protein 1
  • PPARGC1A protein, human
  • Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha
  • Vitamin A