Calcium-myristoyl switch, subcellular localization, and calcium-dependent translocation of the neuronal calcium sensor protein VILIP-3, and comparison with VILIP-1 in hippocampal neurons

Mol Cell Neurosci. 2003 Nov;24(3):766-78. doi: 10.1016/s1044-7431(03)00242-2.

Abstract

Neuronal calcium sensor (NCS) proteins including the subfamily of visinin-like-proteins (VILIPs) are involved in regulation of various signaling cascades. One molecular regulation mechanism is the calcium-myristoyl switch. VILIPs show a calcium-dependent membrane association in brain homogenates; however, differences in calcium-induced conformation changes and degree of membrane association are reported. Little is known about differences in the calcium-myristoyl switch in living cells leading to localization of VILIPs to distinct subcellular compartments. Therefore, we studied the calcium-dependent localization of green fluorescent protein (GFP)-tagged VILIP-3 in living cell lines and hippocampal neurons and compared it with that of GFP-VILIP-1. Interestingly, the observed fast and reversible calcium-myristoyl switch of VILIP-3-GFP and VILIP-1-GFP differed, e.g., in calcium-dependent translocation to Golgi membranes. Similarily, the calcium-dependent localization of endogenously expressed VILIP-3 and -1 in dendrites differed. Thus, VILIPs co-expressed in the same neuron show clear differences in calcium-dependent localization which may allow neurons a highly selective response to various calcium stimuli.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • COS Cells
  • Calcium / metabolism
  • Calcium Signaling / physiology*
  • Calcium-Binding Proteins / metabolism*
  • Cell Compartmentation / physiology
  • Cell Membrane / metabolism
  • Dendrites / metabolism
  • Glutamate Decarboxylase / metabolism
  • Golgi Apparatus / metabolism
  • Green Fluorescent Proteins
  • Hippocampus / cytology
  • Hippocampus / metabolism*
  • Luminescent Proteins
  • Membrane Proteins / metabolism
  • Mice
  • Microtubule-Associated Proteins / metabolism
  • Myristic Acid / metabolism
  • Nerve Tissue Proteins / metabolism*
  • Neurocalcin
  • Neurons / cytology
  • Neurons / metabolism*
  • Potassium Chloride / pharmacology
  • Protein Transport / physiology
  • Qa-SNARE Proteins
  • Rats
  • Receptors, Calcium-Sensing / metabolism*
  • Receptors, Glutamate / drug effects
  • Receptors, Glutamate / metabolism
  • Recombinant Fusion Proteins

Substances

  • Calcium-Binding Proteins
  • Hpcal1 protein, rat
  • Luminescent Proteins
  • Membrane Proteins
  • Microtubule-Associated Proteins
  • Nerve Tissue Proteins
  • Neurocalcin
  • Qa-SNARE Proteins
  • Receptors, Calcium-Sensing
  • Receptors, Glutamate
  • Recombinant Fusion Proteins
  • Vsnl1 protein, mouse
  • Vsnl1 protein, rat
  • Myristic Acid
  • Green Fluorescent Proteins
  • Potassium Chloride
  • Glutamate Decarboxylase
  • Calcium