Increased astrocytic ATP release results in enhanced excitability of the hippocampus

Hae Ung Lee, Yoshihiko Yamazaki, Kenji F. Tanaka, Kishio Furuya, Masahiro Sokabe, Hideki Hida, Keizo Takao, Tsuyoshi Miyakawa, Satoshi Fujii, Kazuhiro Ikenaka

研究成果: Article

24 引用 (Scopus)

抄録

Astrocytes, a major subtype of glia, interact with neurons as a supportive partner supplying energy sources and growth factors. Astrocytes regulate the activity of neighboring neurons by releasing chemical transmitters (gliotransmitters). However, the precise role of gilotransmitters in regulating neuronal activity is still under debate. Here, we report that a subtle enhancement in the release of one gliotransmitter, ATP, affects synaptic potentiation from an analysis of mice containing an astrocyte-selective (GFAP) mutation. We found that, relative to normal mice, weaker stimulation induced long-term potentiation (LTP) in mutant mice, indicating that the threshold to induce LTP was lowered in the mutant. While excitatory transmission was normal in the mutant, inhibitory GABAergic transmission was suppressed. We found that a low concentration of adenosine selectively attenuated inhibitory neuronal activity and lowered the threshold to induce LTP in wild type mice. In comparison, adenosine A1 receptor antagonism reversed the lowered LTP threshold back to normal in the mutant mouse. We verified that adenosine levels in the cerebrospinal fluid of mutant mice were slightly elevated compared to wild type mice. This was apparently caused by an increase in ATP release from mutant astrocytes that could provide a source of augmented adenosine levels in the mutant. ATP is thought to suppress the excitability of neuronal circuits; however, a small increase in ATP release can result in a suppressed inhibitory tone and enhanced excitability of neuronal circuitry. These findings demonstrate that ATP released from astrocytes acts in a bidirectional fashion to regulate neuronal excitability depending on concentration.

元の言語English
ページ(範囲)210-224
ページ数15
ジャーナルGLIA
61
発行部数2
DOI
出版物ステータスPublished - 01-02-2013

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Hippocampus
Adenosine Triphosphate
Astrocytes
Long-Term Potentiation
Adenosine
Adenosine A1 Receptors
Neurons
Neuroglia
Cerebrospinal Fluid
Intercellular Signaling Peptides and Proteins
Mutation

All Science Journal Classification (ASJC) codes

  • Neurology
  • Cellular and Molecular Neuroscience

これを引用

Lee, H. U., Yamazaki, Y., Tanaka, K. F., Furuya, K., Sokabe, M., Hida, H., ... Ikenaka, K. (2013). Increased astrocytic ATP release results in enhanced excitability of the hippocampus. GLIA, 61(2), 210-224. https://doi.org/10.1002/glia.22427
Lee, Hae Ung ; Yamazaki, Yoshihiko ; Tanaka, Kenji F. ; Furuya, Kishio ; Sokabe, Masahiro ; Hida, Hideki ; Takao, Keizo ; Miyakawa, Tsuyoshi ; Fujii, Satoshi ; Ikenaka, Kazuhiro. / Increased astrocytic ATP release results in enhanced excitability of the hippocampus. :: GLIA. 2013 ; 巻 61, 番号 2. pp. 210-224.
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abstract = "Astrocytes, a major subtype of glia, interact with neurons as a supportive partner supplying energy sources and growth factors. Astrocytes regulate the activity of neighboring neurons by releasing chemical transmitters (gliotransmitters). However, the precise role of gilotransmitters in regulating neuronal activity is still under debate. Here, we report that a subtle enhancement in the release of one gliotransmitter, ATP, affects synaptic potentiation from an analysis of mice containing an astrocyte-selective (GFAP) mutation. We found that, relative to normal mice, weaker stimulation induced long-term potentiation (LTP) in mutant mice, indicating that the threshold to induce LTP was lowered in the mutant. While excitatory transmission was normal in the mutant, inhibitory GABAergic transmission was suppressed. We found that a low concentration of adenosine selectively attenuated inhibitory neuronal activity and lowered the threshold to induce LTP in wild type mice. In comparison, adenosine A1 receptor antagonism reversed the lowered LTP threshold back to normal in the mutant mouse. We verified that adenosine levels in the cerebrospinal fluid of mutant mice were slightly elevated compared to wild type mice. This was apparently caused by an increase in ATP release from mutant astrocytes that could provide a source of augmented adenosine levels in the mutant. ATP is thought to suppress the excitability of neuronal circuits; however, a small increase in ATP release can result in a suppressed inhibitory tone and enhanced excitability of neuronal circuitry. These findings demonstrate that ATP released from astrocytes acts in a bidirectional fashion to regulate neuronal excitability depending on concentration.",
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Lee, HU, Yamazaki, Y, Tanaka, KF, Furuya, K, Sokabe, M, Hida, H, Takao, K, Miyakawa, T, Fujii, S & Ikenaka, K 2013, 'Increased astrocytic ATP release results in enhanced excitability of the hippocampus', GLIA, 巻. 61, 番号 2, pp. 210-224. https://doi.org/10.1002/glia.22427

Increased astrocytic ATP release results in enhanced excitability of the hippocampus. / Lee, Hae Ung; Yamazaki, Yoshihiko; Tanaka, Kenji F.; Furuya, Kishio; Sokabe, Masahiro; Hida, Hideki; Takao, Keizo; Miyakawa, Tsuyoshi; Fujii, Satoshi; Ikenaka, Kazuhiro.

:: GLIA, 巻 61, 番号 2, 01.02.2013, p. 210-224.

研究成果: Article

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AU - Lee, Hae Ung

AU - Yamazaki, Yoshihiko

AU - Tanaka, Kenji F.

AU - Furuya, Kishio

AU - Sokabe, Masahiro

AU - Hida, Hideki

AU - Takao, Keizo

AU - Miyakawa, Tsuyoshi

AU - Fujii, Satoshi

AU - Ikenaka, Kazuhiro

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N2 - Astrocytes, a major subtype of glia, interact with neurons as a supportive partner supplying energy sources and growth factors. Astrocytes regulate the activity of neighboring neurons by releasing chemical transmitters (gliotransmitters). However, the precise role of gilotransmitters in regulating neuronal activity is still under debate. Here, we report that a subtle enhancement in the release of one gliotransmitter, ATP, affects synaptic potentiation from an analysis of mice containing an astrocyte-selective (GFAP) mutation. We found that, relative to normal mice, weaker stimulation induced long-term potentiation (LTP) in mutant mice, indicating that the threshold to induce LTP was lowered in the mutant. While excitatory transmission was normal in the mutant, inhibitory GABAergic transmission was suppressed. We found that a low concentration of adenosine selectively attenuated inhibitory neuronal activity and lowered the threshold to induce LTP in wild type mice. In comparison, adenosine A1 receptor antagonism reversed the lowered LTP threshold back to normal in the mutant mouse. We verified that adenosine levels in the cerebrospinal fluid of mutant mice were slightly elevated compared to wild type mice. This was apparently caused by an increase in ATP release from mutant astrocytes that could provide a source of augmented adenosine levels in the mutant. ATP is thought to suppress the excitability of neuronal circuits; however, a small increase in ATP release can result in a suppressed inhibitory tone and enhanced excitability of neuronal circuitry. These findings demonstrate that ATP released from astrocytes acts in a bidirectional fashion to regulate neuronal excitability depending on concentration.

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Lee HU, Yamazaki Y, Tanaka KF, Furuya K, Sokabe M, Hida H その他. Increased astrocytic ATP release results in enhanced excitability of the hippocampus. GLIA. 2013 2 1;61(2):210-224. https://doi.org/10.1002/glia.22427