4.7 Article

P2X4 Receptor Reporter Mice: Sparse Brain Expression and Feeding-Related Presynaptic Facilitation in the Arcuate Nucleus

Journal

JOURNAL OF NEUROSCIENCE
Volume 36, Issue 34, Pages 8902-8920

Publisher

SOC NEUROSCIENCE
DOI: 10.1523/JNEUROSCI.1496-16.2016

Keywords

arcuate; ATP; ion channel; mouse model; P2X; receptor

Categories

Funding

  1. National Institutes of Health [NS073980, NS084030]
  2. University of California-Los Angeles unrestricted funds
  3. National Institute of Alcohol Abuse and Alcoholism Grant [AA022448]
  4. National Institute of Drug Abuse Grant [DA013185]
  5. National Institute on Drug Abuse National Institutes of Health [P50 DA005010]
  6. National Alliance for Research on Schizophrenia and Depression Young Investigator Award
  7. [NS060677]

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P2X4 receptors are ATP-gated cation channels that are widely expressed in the nervous system. To identify P2X4 receptor-expressing cells, we generated BAC transgenic mice expressing tdTomato under the control of the P2X4 receptor gene (P2rx4). We found sparse populations of tdTomato-positive neurons in most brain areas with patterns that matched P2X4 mRNA distribution. tdTomato expression within microglia was low but was increased by an experimental manipulation that triggered microglial activation. We found surprisingly high tdTomato expression in the hypothalamic arcuate nucleus (Arc) (i.e., within parts of the neural circuitry controlling feeding). Immunohistochemistry and genetic crosses of P2rx4 tdTomato mice with cell-specific GFP reporter lines showed that the tdTomato-expressing cells were mainly AgRP-NPY neurons and tanycytes. There was no electrophysiological evidence for functional expression of P2X4 receptors on AgRP-NPY neuron somata, but instead, we found clear evidence for functional presynaptic P2X4 receptor-mediated responses in terminals of AgRP-NPY neurons onto two of their postsynaptic targets (Arc POMC and paraventricular nucleus neurons), where ATP dramatically facilitated GABA release. The presynaptic responses onto POMC neurons, and the expression of tdTomato in AgRP-NPY neurons and tanycytes, were significantly decreased by food deprivation in male mice in a manner that was partially reversed by the satiety-related peptide leptin. Overall, we provide well-characterized tdTomato reporter mice to study P2X4-expressing cells in the brain, new insights on feeding-related regulation of presynaptic P2X4 receptor responses, and the rationale to explore extracellular ATP signaling in the control of feeding behaviors.

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