Trophic factor and hormonal regulation of neurite outgrowth in sensory neuron-like 50B11 cells

Neurosci Lett. 2014 Jan 13:558:120-5. doi: 10.1016/j.neulet.2013.11.018. Epub 2013 Nov 20.

Abstract

Sensory axon integrity and regenerative capacity are important considerations in understanding neuropathological conditions characterized by hyper- or insensitivity. However, our knowledge of mechanisms regulating axon outgrowth are limited by an absence of suitable high-throughput assay systems. The 50B11 cell line generated from rat embryonic dorsal root ganglion neurons offers a promising model for screening assays. Prior characterization shows that these cells express cytoskeletal proteins and genes encoding ion channels and neurotrophin receptors in common with sensory nociceptor neurons. In the present study we further characterized 50B11 cells in regard to their phenotypes and responsiveness to neurotrophic and hormonal factors. 50B11 cells express neuronal cytoplasmic proteins including beta-3 tubulin, peripherin (a marker of unmyelinated neurons), and the pan-neuronal ubiquitin hydrolase, PGP9.5. Only PGP9.5 immunoreactivity was uniformly distributed throughout soma and axons, and therefore presents the best means for visualizing the entire axon arbor. All cells co-express both NGF and GDNF receptors and addition of ligands increased neurite length. 50B11 cells also showed immunoreactivity for the estrogen receptor-α and the angiotensin receptor type II, and both 17-β estradiol and angiotensin II increased outgrowth by differentiated cells. 50B11 cells therefore show features reported previously for primary unmyelinated nociceptor neurons, including responsiveness to classical neurotrophins and hormonal modulators. Coupled with their ease of culture and predictable differentiation, 50B11 cells represent a promising cell line on which to base assays that more clearly reveal mechanisms regulating axon outgrowth and integrity.

Keywords: ANGII; AT2; Axon; DRG; Dorsal root ganglion; E2; ER; GDNF; High throughput screening; Hormones; NGF; Neurotrophic factors; Outgrowth; PGP9.5; angiotensin II; angiotensin II receptor type 2; dorsal root ganglion; estradiol or estrogen; estrogen receptor; glial cell line derived neurotrophic factor; immunoreactivity; ir; nerve growth factor; protein gene product 9.5.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Angiotensin II / pharmacology
  • Animals
  • Cell Differentiation
  • Cell Line / cytology
  • Cell Line / drug effects*
  • Cell Line / ultrastructure
  • Estradiol / pharmacology
  • Estrogens / pharmacology
  • Ganglia, Spinal / cytology
  • Glial Cell Line-Derived Neurotrophic Factor / pharmacology
  • Hormones / pharmacology*
  • Nerve Growth Factor / pharmacology
  • Nerve Growth Factors / pharmacology*
  • Neurites / drug effects*
  • Neurites / physiology
  • Rats
  • Sensory Receptor Cells / cytology
  • Sensory Receptor Cells / drug effects*
  • Sensory Receptor Cells / ultrastructure

Substances

  • Estrogens
  • Glial Cell Line-Derived Neurotrophic Factor
  • Hormones
  • Nerve Growth Factors
  • Angiotensin II
  • Estradiol
  • Nerve Growth Factor