PMID- 10479679 OWN - NLM STAT- MEDLINE DCOM- 19991004 LR - 20191023 IS - 1529-2401 (Electronic) IS - 0270-6474 (Print) IS - 0270-6474 (Linking) VI - 19 IP - 18 DP - 1999 Sep 15 TI - Differential expression of brain-derived neurotrophic factor, neurotrophin-3, and neurotrophin-4/5 in the adult rat spinal cord: regulation by the glutamate receptor agonist kainic acid. PG - 7757-69 AB - Previous in vitro studies indicate that select members of the neurotrophin gene family, namely brain-derived neurotrophic factor (BDNF), neurotrophin-3 (NT-3), and neurotrophin-4/5 (NT-4/5), contribute to survival and differentiation of spinal cord motoneurons. To investigate the potential roles of these factors in the adult spinal cord, we examined their cellular localization and regulation after systemic exposure to an excitotoxic stimulus, kainic acid (KA). Of the neurotrophins examined, NT-4/5 mRNA was most robustly expressed in the lumbosacral spinal cord of the normal adult rat, including expression by neurons throughout the gray matter, and in a subpopulation of white and gray matter glia. Both BDNF and NT-3 mRNAs were also densely expressed by alpha motoneurons of lamina IX, but were detected at lower levels elsewhere in the gray matter. NT-3 mRNA was additionally expressed by spinal cord glia, but was less widespread compared to NT-4/5. In response to systemic administration of KA, NT-4/5 and BDNF mRNAs were dramatically upregulated in a spatially and temporally restricted fashion, whereas levels of NT-3 mRNA were unchanged. These results provide strong in vivo evidence to support the idea that BDNF, NT-3, and in particular, NT-4/5, play a role in the normal function of the adult spinal cord. Furthermore, our results indicate that the actions of BDNF and NT-4/5 participate in the response of the cord to excitotoxic stimuli, and that those of NT-4/5 and NT-3 include both neurons and glia. FAU - Scarisbrick, I A AU - Scarisbrick IA AD - Department of Biochemistry and Molecular Biology, Mayo Clinic Jacksonville, Jacksonville, Florida 32224, USA. FAU - Isackson, P J AU - Isackson PJ FAU - Windebank, A J AU - Windebank AJ LA - eng GR - N01-HD-7-3263/HD/NICHD NIH HHS/United States PT - Journal Article PT - Research Support, U.S. Gov't, P.H.S. PL - United States TA - J Neurosci JT - The Journal of neuroscience : the official journal of the Society for Neuroscience JID - 8102140 RN - 0 (Brain-Derived Neurotrophic Factor) RN - 0 (Excitatory Amino Acid Agonists) RN - 0 (Nerve Growth Factors) RN - 0 (Neuroprotective Agents) RN - 0 (Neurotrophin 3) RN - 0 (RNA, Messenger) RN - 0 (Receptors, Glutamate) RN - 145172-44-7 (neurotrophin 5) RN - P658DCA9XD (neurotrophin 4) RN - SIV03811UC (Kainic Acid) SB - IM MH - Animals MH - Brain-Derived Neurotrophic Factor/*genetics MH - Excitatory Amino Acid Agonists/*pharmacology MH - Gene Expression Regulation/drug effects/*physiology MH - Kainic Acid/*pharmacology MH - Male MH - Nerve Growth Factors/*genetics MH - Neuroglia/*metabolism MH - Neuronal Plasticity MH - Neurons/*metabolism MH - Neuroprotective Agents MH - Neurotrophin 3 MH - RNA, Messenger/genetics MH - Rats MH - Rats, Sprague-Dawley MH - Receptors, Glutamate/*physiology MH - Spinal Cord/cytology/drug effects/*metabolism MH - Transcription, Genetic/*drug effects PMC - PMC6782449 EDAT- 1999/09/10 00:00 MHDA- 1999/09/10 00:01 PMCR- 2000/03/15 CRDT- 1999/09/10 00:00 PHST- 1999/09/10 00:00 [pubmed] PHST- 1999/09/10 00:01 [medline] PHST- 1999/09/10 00:00 [entrez] PHST- 2000/03/15 00:00 [pmc-release] AID - 3430 [pii] AID - 10.1523/JNEUROSCI.19-18-07757.1999 [doi] PST - ppublish SO - J Neurosci. 1999 Sep 15;19(18):7757-69. doi: 10.1523/JNEUROSCI.19-18-07757.1999.