Developmental dysregulation of excitatory-to-inhibitory GABA-polarity switch may underlie schizophrenia pathology: A monozygotic-twin discordant case analysis in human iPS cell-derived neurons
Autor: | Takuya Matsumoto, Kazumichi Hashimoto, Wado Akamatsu, Yasuhiko Saito, Daisuke Ikawa, Shin ichi Fukami, Kyosuke Watanabe, Yohei Okada, Manabu Makinodan, Chieko Aoki, Ryohei Takada, Yoichi Ogawa, Michihiro Toritsuka, Hideyuki Okano, Kazuhiko Yamamuro, Sohei Kimoto, Hiroki Yoshino, Kazuya Okamura, Toshifumi Kishimoto, Kaori Hamano-Iwasa |
---|---|
Rok vydání: | 2021 |
Předmět: |
Male
Pathology medicine.medical_specialty Induced Pluripotent Stem Cells Monozygotic twin Biology Inhibitory postsynaptic potential gamma-Aminobutyric acid Young Adult Cellular and Molecular Neuroscience Glutamatergic medicine Humans Premovement neuronal activity GABAergic Neurons Cells Cultured Neurons Symporters Excitatory Postsynaptic Potentials Cell Differentiation Neural Inhibition Twins Monozygotic Cell Biology Fibroblasts medicine.disease Electrophysiology nervous system Schizophrenia Excitatory postsynaptic potential medicine.drug |
Zdroj: | Neurochemistry International. 150:105179 |
ISSN: | 0197-0186 |
DOI: | 10.1016/j.neuint.2021.105179 |
Popis: | Schizophrenia is a major psychiatric disorder, but the molecular mechanisms leading to its initiation or progression remain unclear. To elucidate the pathophysiology of schizophrenia, we used an in vitro neuronal cell culture model involving human induced pluripotent stem cells (hiPSCs) derived from a monozygotic-twin discordant schizophrenia pair. The cultured neurons differentiated from hiPSCs were composed of a mixture of glutamatergic excitatory neurons and gamma aminobutyric acid (GABA)ergic inhibitory neurons. In the electrophysiological analysis, a different pattern of spontaneous neuronal activity was observed under the condition without any stimulants. The frequency of spontaneous excitatory post-synaptic currents (sEPSCs) was significantly higher in the hiPSC-derived neurons of the patient with schizophrenia than in the control sibling at day-in-vitro 30. However, the synaptic formation was not different between the patient with schizophrenia and the control sibling during the same culture period. To explain underlying mechanisms of higher excitability of presynaptic cells, we focused on the potassium-chloride co-transporter KCC2, which contributes to excitatory-to-inhibitory GABA polarity switch in developing neurons. We also revealed the altered expression pattern of KCC2 in hiPSC-derived neurons from the patient with schizophrenia, which could contribute to understanding the pathology of schizophrenia in the developing nervous system. |
Databáze: | OpenAIRE |
Externí odkaz: |