Astrocyte‐expressed FABP7 regulates dendritic morphology and excitatory synaptic function of cortical neurons. Issue 1 (21st August 2015)
- Record Type:
- Journal Article
- Title:
- Astrocyte‐expressed FABP7 regulates dendritic morphology and excitatory synaptic function of cortical neurons. Issue 1 (21st August 2015)
- Main Title:
- Astrocyte‐expressed FABP7 regulates dendritic morphology and excitatory synaptic function of cortical neurons
- Authors:
- Ebrahimi, Majid
Yamamoto, Yui
Sharifi, Kazem
Kida, Hiroyuki
Kagawa, Yoshiteru
Yasumoto, Yuki
Islam, Ariful
Miyazaki, Hirofumi
Shimamoto, Chie
Maekawa, Motoko
Mitsushima, Dai
Yoshikawa, Takeo
Owada, Yuji - Abstract:
- Abstract : Fatty acid binding protein 7 (FABP7) expressed by astrocytes in developing and mature brains is involved in uptake and transportation of fatty acids, signal transduction, and gene transcription. Fabp7 knockout ( Fabp7 KO) mice show behavioral phenotypes reminiscent of human neuropsychiatric disorders such as schizophrenia. However, direct evidence showing how FABP7 deficiency in astrocytes leads to altered brain function is lacking. Here, we examined neuronal dendritic morphology and synaptic plasticity in medial prefrontal cortex (mPFC) of Fabp7 KO mice and in primary cortical neuronal cultures. Golgi staining of cortical pyramidal neurons in Fabp7 KO mice revealed aberrant dendritic morphology and decreased spine density compared with those in wild‐type (WT) mice. Aberrant dendritic morphology was also observed in primary cortical neurons co‐cultured with FABP7‐deficient astrocytes and neurons cultured in Fabp7 KO astrocyte‐conditioned medium. Excitatory synapse number was decreased in mPFC of Fabp7 KO mice and in neurons co‐cultured with Fabp7 KO astrocytes. Accordingly, whole‐cell voltage‐clamp recording in brain slices from pyramidal cells in the mPFC showed that both amplitude and frequency of action potential‐independent miniature excitatory postsynaptic currents (mEPSCs) were decreased in Fabp7 KO mice. Moreover, transplantation of WT astrocytes into the mPFC of Fabp7 KO mice partially attenuated behavioral impairments. Collectively, these results suggestAbstract : Fatty acid binding protein 7 (FABP7) expressed by astrocytes in developing and mature brains is involved in uptake and transportation of fatty acids, signal transduction, and gene transcription. Fabp7 knockout ( Fabp7 KO) mice show behavioral phenotypes reminiscent of human neuropsychiatric disorders such as schizophrenia. However, direct evidence showing how FABP7 deficiency in astrocytes leads to altered brain function is lacking. Here, we examined neuronal dendritic morphology and synaptic plasticity in medial prefrontal cortex (mPFC) of Fabp7 KO mice and in primary cortical neuronal cultures. Golgi staining of cortical pyramidal neurons in Fabp7 KO mice revealed aberrant dendritic morphology and decreased spine density compared with those in wild‐type (WT) mice. Aberrant dendritic morphology was also observed in primary cortical neurons co‐cultured with FABP7‐deficient astrocytes and neurons cultured in Fabp7 KO astrocyte‐conditioned medium. Excitatory synapse number was decreased in mPFC of Fabp7 KO mice and in neurons co‐cultured with Fabp7 KO astrocytes. Accordingly, whole‐cell voltage‐clamp recording in brain slices from pyramidal cells in the mPFC showed that both amplitude and frequency of action potential‐independent miniature excitatory postsynaptic currents (mEPSCs) were decreased in Fabp7 KO mice. Moreover, transplantation of WT astrocytes into the mPFC of Fabp7 KO mice partially attenuated behavioral impairments. Collectively, these results suggest that astrocytic FABP7 is important for dendritic arbor growth, neuronal excitatory synapse formation, and synaptic transmission, and provide new insights linking FABP7, lipid homeostasis, and neuropsychiatric disorders, leading to novel therapeutic interventions. GLIA 2016;64:48–62 Main Points: We found that astrocyte‐expressed fatty acid binding protein7 (FABP7) is crucial for the normal development of dendritic arbors, neuronal excitatory synapse formation and synaptic transmission through the excitatory synapses of cortical neurons. … (more)
- Is Part Of:
- Glia. Volume 64:Issue 1(2016:Jan.)
- Journal:
- Glia
- Issue:
- Volume 64:Issue 1(2016:Jan.)
- Issue Display:
- Volume 64, Issue 1 (2016)
- Year:
- 2016
- Volume:
- 64
- Issue:
- 1
- Issue Sort Value:
- 2016-0064-0001-0000
- Page Start:
- 48
- Page End:
- 62
- Publication Date:
- 2015-08-21
- Subjects:
- fatty acid binding protein -- glia -- gene knockout mouse -- mEPSCs -- mPFC
Neuroglia -- Periodicals
Neurology -- Periodicals
611.0188 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1098-1136 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/glia.22902 ↗
- Languages:
- English
- ISSNs:
- 0894-1491
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4195.208000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 1713.xml