Subcellular localization and putative role of VPS13A/chorein in dopaminergic neuronal cells

Biochem Biophys Res Commun. 2012 Mar 16;419(3):511-6. doi: 10.1016/j.bbrc.2012.02.047. Epub 2012 Feb 15.

Abstract

Chorea-acanthocytosis (ChAc) is a rare hereditary neurodegenerative disorder caused by loss of function mutations in the vacuolar protein sorting 13 homolog A (VPS13A) gene encoding chorein. Although a deficiency in chorein function leads to apoptosis of striatal neurons in ChAc model mouse, its detailed subcellular localization and physiological role remain unclear. In this study, we produced two anti-chorein polyclonal antibodies and examined the intracellular localization of endogenous chorein in neuronal cells. Immunocytochemically, chorein was observed in the termini of extended neurites and partially colocalized with synaptotagmin I in differentiated PC12 cells. Subcellular localization analysis by sucrose density gradient fractionation showed that chorein and synaptotagmin I were located in dense-core vesicles (DCVs), which contain dopamine. In addition, PC12 cells stably expressing carboxyterminal fragment of chorein increased K(+)-induced dopamine release. Taken together, these results suggest that chorein is involved in exocytosis of DCV.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Line, Tumor
  • Dopaminergic Neurons / metabolism*
  • Exocytosis
  • Humans
  • Mice
  • Nerve Tissue Proteins / genetics
  • Nerve Tissue Proteins / metabolism
  • Neuroacanthocytosis / genetics
  • PC12 Cells
  • Rats
  • Secretory Vesicles / metabolism*
  • Synaptotagmin I / metabolism
  • Vesicular Transport Proteins / genetics
  • Vesicular Transport Proteins / metabolism*

Substances

  • Nerve Tissue Proteins
  • Synaptotagmin I
  • VPS13A protein, human
  • Vesicular Transport Proteins
  • Vps13a protein, mouse