Comparison of expression of inflammatory cytokines in the spinal cord between young adult and aged beagle dogs

Cell Mol Neurobiol. 2013 Jul;33(5):615-24. doi: 10.1007/s10571-013-9915-x. Epub 2013 Apr 20.

Abstract

Aging is an inevitable process that occurs in the whole body system accompanying with many functional and morphological changes. Inflammation is known as one of age-related factors, and inflammatory changes could enhance mortality risk. In this study, we compared immunoreactivities of inflammatory cytokines, such as interleukin (IL)-2 (a pro-inflammatory cytokine), its receptor (IL-2R), IL-4 (an anti-inflammatory cytokine), and its receptor (IL-4R) in the cervical and lumbar spinal cord of young adult (2-3 years old) and aged (10-12 years old) beagle dogs using immunohistochemistry and western blotting. IL-2 and IL-2R-immunoreactive nerve cells were found throughout the gray matter of the cervical and lumbar spinal cord of young adult and aged dogs. In the spinal cord neurons of the aged dog, immunoreactivity and protein levels were apparently increased compared with those in the young adult dog. Change patterns of IL-4- and IL-4R-immunoreactive cells and their protein levels were also similar to those in IL-2 and IL-2R; however, IL-4 and IL-4R immunoreactivity in the periphery of the neuronal cytoplasm in the aged dog was much stronger than that in the young adult dog. These results indicate that the increase of inflammatory cytokines and their receptors in the aged spinal cord might be related to maintaining a balance of inflammatory reaction in the spinal cord during normal aging.

Publication types

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

MeSH terms

  • Aging / pathology*
  • Animals
  • Blotting, Western
  • Dogs
  • Immunohistochemistry
  • Inflammation / pathology*
  • Interleukin-2 / metabolism*
  • Interleukin-4 / metabolism*
  • Receptors, Interleukin-2 / metabolism
  • Receptors, Interleukin-4 / metabolism
  • Spinal Cord / metabolism
  • Spinal Cord / pathology*

Substances

  • Interleukin-2
  • Receptors, Interleukin-2
  • Receptors, Interleukin-4
  • Interleukin-4