Inositol 1, 4, 5-trisphosphate 3-kinase A overexpressed in mouse forebrain modulates synaptic transmission and mGluR-LTD of CA1 pyramidal neurons

Byungil Choi, Hyun Woo Lee, Seojung Mo, Jin Yong Kim, Hyun Wook Kim, Im Joo Rhyu, Eunhwa Hong, Yeon Kyung Lee, June Seek Choi, Chong Hyun Kim, Hyun Kim

Research output: Contribution to journalArticle

2 Citations (Scopus)

Abstract

Inositol 1, 4, 5-trisphosphate 3-kinase A (IP3K-A) regulates the level of the inositol polyphosphates, inositol trisphosphate (IP3) and inositol tetrakisphosphate to modulate cellular signaling and intracellular calcium homeostasis in the central nervous system. IP3K-A binds to F-actin in an activity-dependent manner and accumulates in dendritic spines, where it is involved in the regulation of synaptic plasticity. IP3K-A knockout mice exhibit deficits in some forms of hippocampus-dependent learning and synaptic plasticity, such as long-term potentiation in the dentate gyrus synapses of the hippocampus. In the present study, to further elucidate the role of IP3K-A in the brain, we developed a transgenic (Tg) mouse line in which IP3K-A is conditionally overexpressed approximately 3-fold in the excitatory neurons of forebrain regions, including the hippocampus. The Tg mice showed an increase in both presynaptic release probability of evoked responses, along with bigger synaptic vesicle pools, and miniature excitatory postsynaptic current amplitude, although the spine density or the expression levels of the postsynaptic density-related proteins NR2B, synaptotagmin 1, and PSD-95 were not affected. Hippocampal-dependent learning and memory tasks, including novel object recognition and radial arm maze tasks, were partially impaired in Tg mice. Furthermore, (R, S)-3, 5-dihydroxyphenylglycine-induced metabotropic glutamate receptor long-term depression was inhibited in Tg mice and this inhibition was dependent on protein kinase C but not on the IP3 receptor. Long-term potentiation and depression dependent on N-methyl-d-aspartate receptor were marginally affected in Tg mice. In summary, this study shows that overexpressed IP3K-A plays a role in some forms of hippocampusdependent learning and memory tasks as well as in synaptic transmission and plasticity by regulating both presynaptic and postsynaptic functions.

Original languageEnglish
Article numbere0193859
JournalPLoS One
Volume13
Issue number4
DOIs
Publication statusPublished - 2018 Apr 1

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Inositol 1,4,5-trisphosphate 3-kinase
synaptic transmission
Pyramidal Cells
Prosencephalon
Synaptic Transmission
Transgenic Mice
Neurons
phosphotransferases (kinases)
Phosphotransferases
neurons
Neuronal Plasticity
brain
Inositol
genetically modified organisms
mice
Plasticity
hippocampus
Long-Term Potentiation
Learning
learning

ASJC Scopus subject areas

  • Biochemistry, Genetics and Molecular Biology(all)
  • Agricultural and Biological Sciences(all)

Cite this

Inositol 1, 4, 5-trisphosphate 3-kinase A overexpressed in mouse forebrain modulates synaptic transmission and mGluR-LTD of CA1 pyramidal neurons. / Choi, Byungil; Woo Lee, Hyun; Mo, Seojung; Kim, Jin Yong; Kim, Hyun Wook; Rhyu, Im Joo; Hong, Eunhwa; Lee, Yeon Kyung; Choi, June Seek; Kim, Chong Hyun; Kim, Hyun.

In: PLoS One, Vol. 13, No. 4, e0193859, 01.04.2018.

Research output: Contribution to journalArticle

Choi, Byungil ; Woo Lee, Hyun ; Mo, Seojung ; Kim, Jin Yong ; Kim, Hyun Wook ; Rhyu, Im Joo ; Hong, Eunhwa ; Lee, Yeon Kyung ; Choi, June Seek ; Kim, Chong Hyun ; Kim, Hyun. / Inositol 1, 4, 5-trisphosphate 3-kinase A overexpressed in mouse forebrain modulates synaptic transmission and mGluR-LTD of CA1 pyramidal neurons. In: PLoS One. 2018 ; Vol. 13, No. 4.
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AU - Mo, Seojung

AU - Kim, Jin Yong

AU - Kim, Hyun Wook

AU - Rhyu, Im Joo

AU - Hong, Eunhwa

AU - Lee, Yeon Kyung

AU - Choi, June Seek

AU - Kim, Chong Hyun

AU - Kim, Hyun

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