Grant sponsor: National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK); Grant number: R01DK069351. The content is solely the responsibility of the authors and does not necessarily represent the official views of the NIDDK or the National Institutes of Health; Grant sponsor: National Health and Medical Research Council of Australia; Grant numbers: 1003512 and 1022941, Senior Research Fellowship 632903.
Characterization of axons expressing the artemin receptor in the female rat urinary bladder: A comparison with other major neuronal populations
Version of Record online: 24 JUL 2014
© 2014 Wiley Periodicals, Inc.
Journal of Comparative Neurology
Volume 522, Issue 17, pages 3900–3927, 01 December 2014
How to Cite
Forrest, S. L., Osborne, P. B. and Keast, J. R. (2014), Characterization of axons expressing the artemin receptor in the female rat urinary bladder: A comparison with other major neuronal populations. J. Comp. Neurol., 522: 3900–3927. doi: 10.1002/cne.23648
- Issue online: 16 SEP 2014
- Version of Record online: 24 JUL 2014
- Accepted manuscript online: 10 JUL 2014 04:58AM EST
- Manuscript Accepted: 2 JUL 2014
- Manuscript Revised: 1 JUL 2014
- Manuscript Received: 13 MAY 2014
- neurotrophic factor;
- lower urinary tract;
- pelvic ganglion
Artemin is a member of the glial cell line-derived neurotrophic factor (GDNF) family that has been strongly implicated in development and regeneration of autonomic nerves and modulation of nociception. Whereas other members of this family (GDNF and neurturin) primarily target parasympathetic and nonpeptidergic sensory neurons, the artemin receptor (GFRα3) is expressed by sympathetic and peptidergic sensory neurons that are also the primary sites of action of nerve growth factor, a powerful modulator of bladder nerves. Many bladder sensory neurons express GFRα3 but it is not known if they represent a specific functional subclass. Therefore, our initial aim was to map the distribution of GFRα3-immunoreactive (-IR) axons in the female rat bladder, using cryostat sections and whole wall thickness preparations. We found that GFRα3-IR axons innervated the detrusor, vasculature, and urothelium, but only part of this innervation was sensory. Many noradrenergic sympathetic axons innervating the vasculature were GFRα3-IR, but the noradrenergic innervation of the detrusor was GFRα3-negative. We also identified a prominent source of nonneuronal GFRα3-IR that is likely to be glial. Further characterization of bladder nerves revealed specific structural features of chemically distinct classes of axon terminals, and a major autonomic source of axons labeled with neurofilament-200, which is commonly used to identify myelinated sensory axons within organs. Intramural neurons were also characterized and quantified. Together, these studies reveal a diverse range of potential targets by which artemin could influence bladder function, nerve regeneration, and pain, and provide a strong microanatomical framework for understanding bladder physiology and pathophysiology. J. Comp. Neurol. 522:3900–3927, 2014. © 2014 Wiley Periodicals, Inc.