The Journal of Neuroscience, November 1, 2002, 22(21):9410-9418
Damage-Induced Neuronal Endopeptidase (DINE/ECEL) Expression Is
Regulated by Leukemia Inhibitory Factor and Deprivation of Nerve Growth
Factor in Rat Sensory Ganglia after Nerve Injury
Ryuichi
Kato1, 2,
Sumiko
Kiryu-Seo1, and
Hiroshi
Kiyama1
1 Department of Anatomy and Neurobiology, Graduate
School of Medicine, Osaka City University, Abeno-ku, Osaka, 545-8585, Japan, and 2 Department of Urology, Sapporo Medical
University School of Medicine, Chuo-ku, Sapporo, 060-8543, Japan
Damage-induced neuronal endopeptidase (DINE) is a novel
metallopeptidase and is expressed in response to various neuronal injuries. The expression regulation of DINE mRNA in the dorsal root
ganglia (DRGs) after sciatic nerve injury is examined. A substantial
increase of DINE mRNA expression was observed in relatively small-sized
DRG neurons after nerve injury. The expression was observed in
isolectin B4-negative and partly TrkA-positive neurons, and the
expression profile was fairly similar to that of the neuropeptide galanin. More than 80% of DINE mRNA-positive neurons simultaneously demonstrated galanin immunoreactivity after nerve injury. In cultured DRG, DINE mRNA expression was enhanced by leukemia inhibitory factor
(LIF) but not by other growth factors and cytokines. LIF treatment to
rat sciatic nerve induced DINE mRNA expression in DRG without nerve
injury, and, conversely, the intranerve injection of anti-gp130
antibody after sciatic nerve injury significantly inhibited the
upregulation of DINE mRNA in DRG. Furthermore, nerve growth factor
(NGF) deprivation, which can induce galanin expression, also enhanced
DINE mRNA expression in vitro and in
vivo. Both LIF application and NGF deprivation additively
enhanced DINE expression in vitro. These results suggest
that DINE gene expression is regulated separately by both LIF and NGF
deprivation, and this regulation pattern is similar to that of galanin
gene expression. Because both DINE and galanin have a neuroprotective
function, their simultaneous induction may provide more successful
protection for injured sensory neurons.
Key words:
peptidase; gene expression; dorsal root ganglion; nerve
injury; galanin; LIF; NGF deprivation
Copyright © 2002 Society for Neuroscience 0270-6474/02/22219410-09$05.00/0