Regulated endosomal trafficking of Diacylglycerol lipase alpha (DAGLα) generates distinct cellular pools; implications for endocannabinoid signaling

Mol Cell Neurosci. 2016 Oct:76:76-86. doi: 10.1016/j.mcn.2016.08.011. Epub 2016 Sep 3.

Abstract

Diacylglycerol lipase alpha (DAGLα) generates the endocannabinoid (eCB) 2-arachidonylglycerol (2-AG) that regulates the proliferation and differentiation of neural stem cells and serves as a retrograde signaling lipid at synapses. Nothing is known about the dynamics of DAGLα expression in cells and this is important as it will govern where 2-AG can be made and released. We have developed a new construct to label DAGLα at the surface of live cells and follow its trafficking. In hippocampal neurons a cell surface pool of DAGLα co-localizes with Homer, a postsynaptic density marker. This surface pool of DAGLα is dynamic, undergoing endocytosis and recycling back to the postsynaptic membrane. A similar cycling is seen in COS-7 cells with the internalized DAGLα initially transported to EEA1 and Rab5-positive early endosomes via a clathrin-independent pathway before being transported back to the cell surface. The internalized DAGLα is present on reticular structures that co-localize with microtubules. Importantly, DAGLα cycling is a regulated process as inhibiting PKC results in a significant reduction in endocytosis. This is the first description of DAGLα cycling between the cell surface and an intracellular endosomal compartment in a manner that can regulate the level of the enzyme at the cell surface.

Keywords: 2-AG; DAGLα; Endocannabinoid; Endocytosis; Endosomes; Trafficking.

MeSH terms

  • Animals
  • COS Cells
  • Cell Membrane / metabolism*
  • Chlorocebus aethiops
  • Endocannabinoids / metabolism*
  • Endocytosis
  • Endosomes / metabolism*
  • Hippocampus / cytology
  • Hippocampus / metabolism
  • Lipoprotein Lipase / metabolism*
  • Neurons / metabolism
  • Post-Synaptic Density / metabolism
  • Protein Kinase C / metabolism
  • Rats
  • Rats, Sprague-Dawley
  • Signal Transduction*

Substances

  • Endocannabinoids
  • Protein Kinase C
  • Lipoprotein Lipase