QUICK SEARCH:   [advanced] Author: Keyword(s): Year:  Vol:  Page:

HOME  |   SEARCH  |   ARCHIVE  |   SUBSCRIBE  |   CONTACT  |   HELP

The Journal of Neuroscience, July 5, 2006, 26(27):7281-7292; doi:10.1523/JNEUROSCI.1072-06.2006

This Article Full Text Full Text (PDF) Submit an eLetter Alert me when this article is cited Alert me when eLetters are posted Alert me if a correction is posted Citation Map Services Email this article to a friend Related articles in J. Neurosci. Similar articles in this journal Similar articles in Web of Science Similar articles in PubMed Alert me to new issues of the journal Download to citation manager Citing Articles Citing Articles via HighWire Citing Articles via Web of Science (40) Citing Articles via Google Scholar Google Scholar Articles by Fang, X. Articles by Lawson, S. N. Search for Related Content PubMed PubMed Citation Articles by Fang, X. Articles by Lawson, S. N.

 Previous Article  |  Next Article 

Cellular/Molecular
Intense Isolectin-B4 Binding in Rat Dorsal Root Ganglion Neurons Distinguishes C-Fiber Nociceptors with Broad Action Potentials and High Nav1.9 Expression

Xin Fang,¹ Laiche Djouhri,¹ Simon McMullan,¹ Carol Berry,¹ Stephen G. Waxman,² Kenji Okuse,³ and Sally N. Lawson¹

¹Department of Physiology, Medical School, Bristol University, Bristol BS8 1TD, United Kingdom, ²Department of Neurology, Yale University School of Medicine, New Haven, Connecticut 06510, and ³Division of Cell and Molecular Biology, Faculty of Life Sciences, Imperial College London, London SW7 2AZ, United Kingdom

Correspondence should be addressed to Prof. Sally N. Lawson, Department of Physiology, Medical School, University of Bristol, University Walk, Bristol BS8 1TD, UK. Email: Sally.Lawson{at}bristol.ac.uk

Binding to isolectin-B4 (IB4) and expression of tyrosine kinase A (trkA) (the high-affinity NGF receptor) have been used to define two different subgroups of nociceptive small dorsal root ganglion (DRG) neurons. We previously showed that only nociceptors have high trkA levels. However, information about sensory and electrophysiological properties in vivo of single identified IB4-binding neurons, and about their trkA expression levels, is lacking. IB4-positive (IB4+) and small dark neurons had similar size distributions. We examined IB4-binding levels in >120 dye-injected DRG neurons with sensory and electrophysiological properties recorded in vivo. Relative immunointensities for trkA and two TTX-resistant sodium channels (Nav1.8 and Nav1.9) were also measured in these neurons. IB4+ neurons were classified as strongly or weakly IB4+.

All strongly IB4+ neurons were C-nociceptor type (C-fiber nociceptive or unresponsive). Of 32 C-nociceptor-type neurons examined, 50% were strongly IB4+, 20% were weakly IB4+ and 30% were IB4–. A low-threshold mechanoreceptive (LTM) neurons were weakly IB4+ or IB4–. All 33 A-fiber nociceptors and all 44 A/-LTM neurons examined were IB4–. IB4+ compared with IB4– C-nociceptor-type neurons had longer somatic action potential durations and rise times, slower conduction velocities, more negative membrane potentials, and greater immunointensities for Nav1.9 but not Nav1.8. Immunointensities of IB4 binding in C-neurons were positively correlated with those of Nav1.9 but not Nav1.8. Of 23 C-neurons tested for both trkA and IB4, 35% were trkA+/IB4+ but with negatively correlated immunointensities; 26% were IB4+/trkA–, and 35% were IB4–/trkA+. We conclude that strongly IB4+ DRG neurons are exclusively C-nociceptor type and that high Nav1.9 expression may contribute to their distinct membrane properties.

Key words: IB4; nociceptive; sodium channel; action potential; trkA; DRG; pain; NGF

---

Received March 12, 2006; revised May 31, 2006; accepted May 31, 2006.

Correspondence should be addressed to Prof. Sally N. Lawson, Department of Physiology, Medical School, University of Bristol, University Walk, Bristol BS8 1TD, UK. Email: Sally.Lawson{at}bristol.ac.uk

Related articles in J. Neurosci.:

This Week in The Journal

J. Neurosci. 2006 26: i. [Full Text]  

This article has been cited by other articles:

				S. A. Malin, J. A. Christianson, K. Bielefeldt, and B. M. Davis TRPV1 Expression Defines Functionally Distinct Pelvic Colon Afferents J. Neurosci., January 21, 2009; 29(3): 743 - 752. [Abstract] [Full Text] [PDF]

				F. Maingret, B. Coste, F. Padilla, N. Clerc, M. Crest, S. M. Korogod, and P. Delmas Inflammatory Mediators Increase Nav1.9 Current and Excitability in Nociceptors through a Coincident Detection Mechanism J. Gen. Physiol., February 25, 2008; 131(3): 211 - 225. [Abstract] [Full Text] [PDF]

				J. A. R. Ostman, M. A. Nassar, J. N. Wood, and M. D. Baker GTP up-regulated persistent Na+ current and enhanced nociceptor excitability require NaV1.9 J. Physiol., February 15, 2008; 586(4): 1077 - 1087. [Abstract] [Full Text] [PDF]

				M. D. Boada and C. J. Woodbury Physiological Properties of Mouse Skin Sensory Neurons Recorded Intracellularly In Vivo: Temperature Effects on Somal Membrane Properties J Neurophysiol, August 1, 2007; 98(2): 668 - 680. [Abstract] [Full Text] [PDF]

				A. M. Rush, T. R. Cummins, and S. G. Waxman Multiple sodium channels and their roles in electrogenesis within dorsal root ganglion neurons J. Physiol., February 15, 2007; 579(1): 1 - 14. [Abstract] [Full Text] [PDF]

				J.-S. Choi, S. D. Dib-Hajj, and S. G. Waxman Differential Slow Inactivation and Use-Dependent Inhibition of Nav1.8 Channels Contribute to Distinct Firing Properties in IB4+ and IB4- DRG Neurons J Neurophysiol, February 1, 2007; 97(2): 1258 - 1265. [Abstract] [Full Text] [PDF]

				B. Coste, M. Crest, and P. Delmas Pharmacological Dissection and Distribution of NaN/Nav1.9, T-type Ca2+ Currents, and Mechanically Activated Cation Currents in Different Populations of DRG Neurons J. Gen. Physiol., January 1, 2007; 129(1): 57 - 77. [Abstract] [Full Text] [PDF]

Home  |   Search  |   Archive  |   Subscribe  |   Contact  |   Help