Vitamin D regulation of GDNF/Ret signaling in dopaminergic neurons

FASEB J. 2018 Feb;32(2):819-828. doi: 10.1096/fj.201700713R. Epub 2018 Jan 4.

Abstract

1,25(OH)2D3 (vitamin D) appears essential for the normal development of dopaminergic neurons. Vitamin D affects dopamine synthesis and metabolism as well as expression of glial cell line-derived neurotrophic factor (GDNF), which is crucial for the survival of dopaminergic neurons. We investigated the role of vitamin D on GDNF and its receptors protooncogene tyrosine-protein kinase receptor Ret (C-Ret) and GDNF family receptor alpha 1 (GFRα1) signaling. To this end, we used a developmental vitamin D-deficient rat model and SH-SY5Y cells transfected with vitamin D receptor (VDR). The absence of vitamin D ligand in gestation reduces C-Ret expression, but not GDNF and GFRα1, in embryo forebrains. Overexpression of VDR in SH-SY5Y in the absence of ligand (mimicking in vivo developmental vitamin D deficiency) also suppressed C-Ret mRNA levels. In the presence of vitamin D, C-Ret mRNA and protein expression were increased. The chromatin immunoprecipitation results suggested that C-Ret is directly regulated by vitamin D via VDR. GDNF was also increased by vitamin D in these cells. Our small interfering RNA studies showed that knocking down VDR leads to an increase in C-Ret in the absence of ligand. Finally, we confirmed the inverse relationship between GFRα1 and C-Ret, as knocking down C-Ret led to increases in GFRα1 expression. These data extend our knowledge of the diverse and important roles played by vitamin D in dopamine physiology.-Pertile, R. A. N., Cui, X., Hammond, L., Eyles, D. W. Vitamin D regulation of GDNF/Ret signaling in dopaminergic neurons.

Keywords: C-Ret; DVD-deficiency; GFRα1; SH-SY5Y; VDR.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Line, Tumor
  • Dopaminergic Neurons / cytology
  • Dopaminergic Neurons / metabolism*
  • Female
  • Gene Expression Regulation / physiology
  • Glial Cell Line-Derived Neurotrophic Factor / metabolism*
  • Humans
  • Proto-Oncogene Proteins c-ret / metabolism*
  • Rats
  • Rats, Sprague-Dawley
  • Receptors, Calcitriol / metabolism
  • Signal Transduction / physiology*
  • Vitamin D / metabolism*

Substances

  • Glial Cell Line-Derived Neurotrophic Factor
  • Receptors, Calcitriol
  • Vitamin D
  • Proto-Oncogene Proteins c-ret
  • RET protein, human
  • Ret protein, rat