Comparative analysis of P2X1, P2X2, P2X3, and P2X4 receptor subunits in rat nodose ganglion neurons

PLoS One. 2014 May 5;9(5):e96699. doi: 10.1371/journal.pone.0096699. eCollection 2014.

Abstract

Nodose ganglion (NG) neurons are visceral primary sensory neurons. The transmission and regulation of visceral sensation is mediated mainly by the P2X purinoceptor (P2X receptor). Although the characteristics of different P2X receptor subunits in the NG have been studied previously, comprehensive analyses have not been performed. In this study, we used immunohistochemistry, immunocytochemistry, and whole cell patch clamp techniques to compare the expression and function of P2X1, P2X2, P2X3, and P2X4 receptor subunits in adult rat NG neurons. Polyclonal antibodies against the four P2X subunits labeled different subpopulations of NG neurons. P2X1 and P2X3 were expressed mainly in small-to-medium sized NG neurons, whereas P2X2 and P2X4 were located mostly in medium- and larger-sized NG neurons. Over 36% of NG neurons were P2X3 positive, which was higher than the other three P2X subunits. In addition, different types of currents were recorded from neurons expressing different P2X subunits. The fast type of ATP current was recorded from neurons containing P2X1-4 subunits, the intermediate type of current was recorded from neurons containing the P2X1, P2X3, and P2X4 subunits, the slow type was recorded from neurons expressing P2X1-3, and/or P2X4 subunits, whereas the very slow type was recorded from neurons containing the P2X2 and P2X3 subunits. These comparative results provide an anatomical verification of the different subunits in NG neurons, and offer direct support for the idea that various functional NG populations have distinct responses to ATP, which might be in part due to the different expression profiles of diverse P2X subunits.

Publication types

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

MeSH terms

  • Adenosine Triphosphate / metabolism
  • Animals
  • Gene Expression Profiling
  • Gene Expression Regulation
  • Immunohistochemistry
  • Male
  • Microscopy, Fluorescence
  • Neurons / metabolism
  • Nodose Ganglion / metabolism*
  • Patch-Clamp Techniques
  • Rats
  • Rats, Sprague-Dawley
  • Receptors, Purinergic P2X1 / metabolism*
  • Receptors, Purinergic P2X2 / metabolism*
  • Receptors, Purinergic P2X3 / metabolism*
  • Receptors, Purinergic P2X4 / metabolism*

Substances

  • Receptors, Purinergic P2X1
  • Receptors, Purinergic P2X2
  • Receptors, Purinergic P2X3
  • Receptors, Purinergic P2X4
  • Adenosine Triphosphate

Grants and funding

This work was supported by grants from the National Natural Science Foundation of China (81200863 to L. Pei, 81260211 to Z. Wang) and China Postdoctoral Science Foundation (2013M530345 and 2013M540583 to L. Pei). Shanghai Chempartner provided support in the form of a salary for author L. Wang, but did not have any additional role in the study design, data collection and analysis, decision to publish, or preparation of the manuscript.