Analyze Diet
Microscopy research and technique2011; 75(5); 626-637; doi: 10.1002/jemt.21102

Expression of high-molecular-mass neurofilament protein in horse (Equus caballus) spinal ganglion neurons.

Abstract: Spinal ganglion (SG) neurons are subdivided, on the basis of their cytoplasmic aspect at light and electron microscopy, into dark (D) and light (L) neurons. Numerous efforts have been made to find specific markers able to identify D and L neuronal cytotypes. The isolectin B4 (IB4), utilized to identify nonpeptidergic D neurons in mice, unfortunately, has not proved as effective in other species. The 200-kDa neurofilament protein (NF200) is considered as a typical marker of L neurons in the rat, cat, and chick. The aim of this study was to analyze the histological, morphometric, and neurochemical characteristic of NF200-immunoreactive (IR) horse SG neurons, to better characterize them morphologically and functionally. NF200-IR neurons showed two levels (strong and weak) of staining intensity. Most (84%) strongly stained NF200-IR neurons corresponded to L neurons, and showed similar bimodality as in the size distribution study, which seems to indicate a third population of neurons, in addition to the two populations (small and large) previously identified. In triple-staining experiments where NF200 was colocalized with IB4, substance P (SP), and neuronal nitric oxide synthase (nNOS) neuronal markers, most NF200-IR neurons were single stained. On the contrary, most IB4-, SP-, and nNOS-stained neurons were triple labeled and almost equally subdivided between strong and weak NF200-IR with the latter being always smaller in size than strong NF200-IR neurons. In conclusion, horse SG neurons display significant morphometric and neurochemical differences compared with those of rodents.
Publication Date: 2011-10-28 PubMed ID: 22038722DOI: 10.1002/jemt.21102Google Scholar: Lookup
The Equine Research Bank provides access to a large database of publicly available scientific literature. Inclusion in the Research Bank does not imply endorsement of study methods or findings by Mad Barn.
  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

This research summary has been generated with artificial intelligence and may contain errors and omissions. Refer to the original study to confirm details provided. Submit correction.

The research paper is an investigation into the characteristics of neurons in horse spinal ganglions, specifically those immunoreactive to the 200-kDa neurofilament protein, highlighting significant morphometric and neurochemical differences when compared with those of rodents.

Key Objective and Methodology

  • The primary aim of this study was to thoroughly explore the histological, morphometric, and neurochemical features of horse spinal ganglion (SG) neurons that display immunoreactivity (IR) to the 200-kDa neurofilament protein (NF200), intending to offer more comprehensive morphological and functional characterizations.
  • The researchers conducted a series of experiments including the utilization of stained neurons that responded to NF200, isolectin B4 (IB4), substance P (SP), and neuronal nitric oxide synthase (nNOS).

Key Findings

  • Two levels of staining intensity were observed. Neurons exhibiting strong NF200-IR staining made up the majority at 84%, typically correlating with Light (L) neurons. Others showed weak staining response.
  • The study identified possible existence of a third neuronal population apart from the two already known sizes (small and large), on the basis of size distribution and staining intensity.
  • Triple-staining experiments were performed to analyze how NF200 colocalizes with other neuronal markers, IB4, SP, and nNOS. The results highlighted that the majority of NF200-IR neurons were single-stained, while most neurons stained with IB4, SP, and nNOS were triple labeled.
  • The study found that the strongly and weakly stained NF200-IR neurons from triple-staining were almost equally distributed. They also found that weak NF200-IR neurons were consistently smaller in size compared to the strongly stained ones.

Conclusion

  • The research concluded that there are considerable morphometric and neurochemical differences in horse SG neurons when compared with those seen in rodents. Such findings could advance our understanding of not only the morphological diversity among different species but also the varied roles and functions these neurons undertake within the spinal system.

Cite This Article

APA
Russo D, Castellani G, Chiocchetti R. (2011). Expression of high-molecular-mass neurofilament protein in horse (Equus caballus) spinal ganglion neurons. Microsc Res Tech, 75(5), 626-637. https://doi.org/10.1002/jemt.21102

Publication

ISSN: 1097-0029
NlmUniqueID: 9203012
Country: United States
Language: English
Volume: 75
Issue: 5
Pages: 626-637

Researcher Affiliations

Russo, Domenico
  • Department of Veterinary Medical Science, University of Bologna, Bologna, Italy. domrusso@unina.it
Castellani, Gastone
    Chiocchetti, Roberto

      MeSH Terms

      • Animals
      • Ganglia, Spinal / chemistry
      • Ganglia, Spinal / cytology
      • Horses
      • Microscopy, Fluorescence
      • Molecular Weight
      • Neurofilament Proteins / analysis
      • Neurons / chemistry
      • Neurons / cytology

      Citations

      This article has been cited 1 times.
      1. Gilbert MT, Soderstrom K. Developmental but not adult cannabinoid treatments persistently alter axonal and dendritic morphology within brain regions important for zebra finch vocal learning. Brain Res 2014 Apr 16;1558:57-73.