Cited by 122Nerve injury and regenerationTraumatic Brain Injury and Neurovascular DisturbancesNeurogenesis and neuroplasticity mechanisms

Differential expression of sgk mRNA, a member of the Ser/Thr protein kinase gene family, in rat brain after CNS injury

Imaizumi, K., Tsuda, M., Wanaka, A., Tohyama, M., Takagi, T.·1994·Molecular Brain Research

Abstract

We cloned genes the expression of which were induced 3 days after cortical injury of rat brain by a differential display technique, and four novel and known sequences were isolated. Among these sequences, the sgk gene which was recently identified as a novel member of the serine/threonine protein kinase gene family, was selected for analysis of its expression patterns in rat brain by northern blotting and in situ hybridization, because hybridization signals were strong at the lesion sites. Expression of sgk mRNA was induced within 3 days after injury, and was maintained at a high level for at least 14 days. The cells which strongly expressed the sgk gene were in the deep layers of the cortex and in the corpus callosum. In situ hybridization analysis for sgk and myelin proteolipid protein mRNA using serial sections showed that the distribution of both signals was very similar at the damaged regions. Therefore, it is likely that the sgk transcript is expressed by oligodendrocytes after brain injury. Investigation of the developmental expression of the sgk gene showed that neurons in layers I and II of the cortex, lateroposterior and laterodorsal thalamic nucleus, and ventral posterolateral and posteromedial thalamic nucleus strongly expressed sgk mRNA at postnatal day 1 and day 7, but these neurons showed no expression in fetal or adult brain. These results suggest that the induction of sgk gene may be associated with a series of axonal regenerations after brain injury, and in…

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Crossref · 10.1016/0169-328x(94)90090-6

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  • In rats, SGK1 transcription levels are markedly induced in neuron and oligodendrocyte area following cortical injury, with significant elevation by day three and sustained high expression for up to 14 days.

    “In rats, SGK1 transcription levels are markedly induced in the neuron and oligodendrocyte area following cortical injury, with significant elevation observed by day three and sustained high expression levels for up to 14 days”
  • After TBI, loss of myelination can trigger neuroinflammation and upregulation of SGK1 transcription levels in oligodendrocytes.

    “After TBI, the loss of myelination can trigger neuroinflammation and upregulation of SGK1 transcription levels in oligodendrocytes”

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References 29 · Cited by 122

Authors
Imaizumi, K., Tsuda, M., Wanaka, A., Tohyama, M., & Takagi, T.
Affiliations
The University of Osaka (JP)
Corresponding author
Imaizumi, K.
Venue
Molecular Brain Research
Publisher
Elsevier BV
Published
1994-10
Volume
26
Issue
1-2
Pages
189-196
ISSN
0169-328X (ISSN-L)
OpenAlex
W1973855704
Cited by
122
References
29
Citations by year
2024: 1 · 2023: 7 · 2022: 1 · 2021: 1 · 2020: 1 · 2017: 2 · 2016: 2 · 2015: 2 · 2014: 1 · 2013: 2 · 2012: 1
FWCI
1.68
Type
journal article
Language
en
Open access
closed
Locations
  • Molecular Brain Research (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Nerve injury and regeneration
  • Health Sciences › Medicine › Neurology › Traumatic Brain Injury and Neurovascular Disturbances
  • Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
Keywords
serine/threonine kinase, gene expression, cortical injury, brain injury, oligodendrocytes, myelin proteolipid protein, axon regeneration, thalamic nuclei, postnatal brain development, rat brain
MeSH terms
Serum-Glucocorticoid Regulated Kinases, Aging, Animals, Animals, Newborn, Base Sequence, Brain, Brain Injuries, Cerebral Cortex, Cloning, Molecular, Corpus Striatum, Hippocampus, Immunohistochemistry, Male, Molecular Sequence Data, Nerve Regeneration, Nuclear Proteins, RNA, Messenger, Thalamus, Transcription, Genetic, Blotting, Northern, RNA Probes, Gene Expression Regulation, Enzymologic, Polymerase Chain Reaction, Rats, Wistar, Protein Serine-Threonine Kinases, In Situ Hybridization, Immediate-Early Proteins, DNA Primers, Rats

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