-
Je něco špatně v tomto záznamu ?
Clozapine Reverses Dysfunction of Glutamatergic Neurons Derived From Clozapine-Responsive Schizophrenia Patients
H. Hribkova, O. Svoboda, E. Bartecku, J. Zelinkova, J. Horinkova, L. Lacinova, M. Piskacek, B. Lipovy, I. Provaznik, JC. Glover, T. Kasparek, YM. Sun
Jazyk angličtina Země Švýcarsko
Typ dokumentu časopisecké články
NLK
Directory of Open Access Journals
od 2007
Free Medical Journals
od 2007
PubMed Central
od 2007
Europe PubMed Central
od 2007
Open Access Digital Library
od 2007-01-01
Open Access Digital Library
od 2007-01-01
ROAD: Directory of Open Access Scholarly Resources
od 2007
- Publikační typ
- časopisecké články MeSH
The cellular pathology of schizophrenia and the potential of antipsychotics to target underlying neuronal dysfunctions are still largely unknown. We employed glutamatergic neurons derived from induced pluripotent stem cells (iPSC) obtained from schizophrenia patients with known histories of response to clozapine and healthy controls to decipher the mechanisms of action of clozapine, spanning from molecular (transcriptomic profiling) and cellular (electrophysiology) levels to observed clinical effects in living patients. Glutamatergic neurons derived from schizophrenia patients exhibited deficits in intrinsic electrophysiological properties, synaptic function and network activity. Deficits in K+ and Na+ currents, network behavior, and glutamatergic synaptic signaling were restored by clozapine treatment, but only in neurons from clozapine-responsive patients. Moreover, neurons from clozapine-responsive patients exhibited a reciprocal dysregulation of gene expression, particularly related to glutamatergic and downstream signaling, which was reversed by clozapine treatment. Only neurons from clozapine responders showed return to normal function and transcriptomic profile. Our results underscore the importance of K+ and Na+ channels and glutamatergic synaptic signaling in the pathogenesis of schizophrenia and demonstrate that clozapine might act by normalizing perturbances in this signaling pathway. To our knowledge this is the first study to demonstrate that schizophrenia iPSC-derived neurons exhibit a response phenotype correlated with clinical response to an antipsychotic. This opens a new avenue in the search for an effective treatment agent tailored to the needs of individual patients.
Department of Biology Masaryk University Brno Czechia
Department of Molecular Medicine Institute of Basic Medical Sciences University of Oslo Oslo Norway
Department of Pathological Physiology Masaryk University Brno Czechia
Department of Physiology Faculty of Medicine Masaryk University Brno Czechia
Department of Psychiatry Faculty of Medicine and University Hospital Brno Brno Czechia
Citace poskytuje Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc22009945
- 003
- CZ-PrNML
- 005
- 20220425131631.0
- 007
- ta
- 008
- 220420s2022 sz f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.3389/fncel.2022.830757 $2 doi
- 035 __
- $a (PubMed)35281293
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a sz
- 100 1_
- $a Hribkova, Hana $u Department of Biology, Masaryk University, Brno, Czechia
- 245 10
- $a Clozapine Reverses Dysfunction of Glutamatergic Neurons Derived From Clozapine-Responsive Schizophrenia Patients / $c H. Hribkova, O. Svoboda, E. Bartecku, J. Zelinkova, J. Horinkova, L. Lacinova, M. Piskacek, B. Lipovy, I. Provaznik, JC. Glover, T. Kasparek, YM. Sun
- 520 9_
- $a The cellular pathology of schizophrenia and the potential of antipsychotics to target underlying neuronal dysfunctions are still largely unknown. We employed glutamatergic neurons derived from induced pluripotent stem cells (iPSC) obtained from schizophrenia patients with known histories of response to clozapine and healthy controls to decipher the mechanisms of action of clozapine, spanning from molecular (transcriptomic profiling) and cellular (electrophysiology) levels to observed clinical effects in living patients. Glutamatergic neurons derived from schizophrenia patients exhibited deficits in intrinsic electrophysiological properties, synaptic function and network activity. Deficits in K+ and Na+ currents, network behavior, and glutamatergic synaptic signaling were restored by clozapine treatment, but only in neurons from clozapine-responsive patients. Moreover, neurons from clozapine-responsive patients exhibited a reciprocal dysregulation of gene expression, particularly related to glutamatergic and downstream signaling, which was reversed by clozapine treatment. Only neurons from clozapine responders showed return to normal function and transcriptomic profile. Our results underscore the importance of K+ and Na+ channels and glutamatergic synaptic signaling in the pathogenesis of schizophrenia and demonstrate that clozapine might act by normalizing perturbances in this signaling pathway. To our knowledge this is the first study to demonstrate that schizophrenia iPSC-derived neurons exhibit a response phenotype correlated with clinical response to an antipsychotic. This opens a new avenue in the search for an effective treatment agent tailored to the needs of individual patients.
- 655 _2
- $a časopisecké články $7 D016428
- 700 1_
- $a Svoboda, Ondrej $u Department of Biomedical Engineering, Faculty of Electrical Engineering and Communication, Brno University of Technology, Brno, Czechia
- 700 1_
- $a Bartecku, Elis $u Department of Psychiatry, Faculty of Medicine and University Hospital Brno, Brno, Czechia
- 700 1_
- $a Zelinkova, Jana $u Department of Biology, Masaryk University, Brno, Czechia
- 700 1_
- $a Horinkova, Jana $u Department of Psychiatry, Faculty of Medicine and University Hospital Brno, Brno, Czechia
- 700 1_
- $a Lacinova, Lubica $u Center of Bioscience, Institute of Molecular Physiology and Genetics, Slovak Academy of Sciences, Bratislava, Slovakia
- 700 1_
- $a Piskacek, Martin $u Department of Pathological Physiology, Masaryk University, Brno, Czechia
- 700 1_
- $a Lipovy, Bretislav $u Department of Burns and Plastic Surgery, Faculty of Medicine and University Hospital Brno, Brno, Czechia
- 700 1_
- $a Provaznik, Ivo $u Department of Biomedical Engineering, Faculty of Electrical Engineering and Communication, Brno University of Technology, Brno, Czechia $u Department of Physiology, Faculty of Medicine, Masaryk University, Brno, Czechia
- 700 1_
- $a Glover, Joel C $u Department of Molecular Medicine, Institute of Basic Medical Sciences, University of Oslo, Oslo, Norway $u Norwegian Center for Stem Cell Research, Department of Immunology and Transfusion Medicine, Oslo University Hospital, Oslo, Norway
- 700 1_
- $a Kasparek, Tomas $u Department of Psychiatry, Faculty of Medicine and University Hospital Brno, Brno, Czechia
- 700 1_
- $a Sun, Yuh-Man $u Department of Biology, Masaryk University, Brno, Czechia
- 773 0_
- $w MED00163312 $t Frontiers in cellular neuroscience $x 1662-5102 $g Roč. 16, č. - (2022), s. 830757
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/35281293 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y - $z 0
- 990 __
- $a 20220420 $b ABA008
- 991 __
- $a 20220425131629 $b ABA008
- 999 __
- $a ind $b bmc $g 1784445 $s 1161143
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2022 $b 16 $c - $d 830757 $e 20220223 $i 1662-5102 $m Frontiers in cellular neuroscience $n Front Cell Neurosci $x MED00163312
- LZP __
- $a Pubmed-20220420