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Abnormal gene expression of BDNF, but not BDNF-AS, in iPSC, neural stem cells and postmortem brain samples from bipolar disorder.
Ishima, Tamaki; Illes, Sebastian; Iwayama, Yoshimi; Dean, Brian; Yoshikawa, Takeo; Ågren, Hans; Funa, Keiko; Hashimoto, Kenji.
Afiliação
  • Ishima T; Division of Clinical Neuroscience, Chiba University Center for Forensic Mental Health, Chiba, Japan.
  • Illes S; Institute of Neuroscience and Physiology, Sahlgrenska Academy, Gothenburg University, Gothenburg, Sweden.
  • Iwayama Y; Laboratory of Molecular Psychiatry, RIKEN Center for Brain Science, Wako, Saitama, Japan; Support Unit for Bio-Material Analysis, Research Resources Division, RIKEN Center for Brain Science, Wako, Saitama, Japan.
  • Dean B; The Florey Institute of Neuroscience and Mental Health, Howard Florey Laboratories, The University of Melbourne, Parkville, Victoria, Australia; The Centre for Mental Health, Swinburne University, Hawthorn, Victoria, Australia.
  • Yoshikawa T; Laboratory of Molecular Psychiatry, RIKEN Center for Brain Science, Wako, Saitama, Japan.
  • Ågren H; Institute of Neuroscience and Physiology, Sahlgrenska Academy, Gothenburg University, Gothenburg, Sweden.
  • Funa K; Sahlgrenska Cancer Center, Institute of Biomedicine, Sahlgrenska Academy, Gothenburg University, Gothenburg, Sweden; Oncology Laboratory, Department of Pathology, Sahlgrenska University Hospital, Gothenburg, Sweden.
  • Hashimoto K; Division of Clinical Neuroscience, Chiba University Center for Forensic Mental Health, Chiba, Japan. Electronic address: hashimoto@faculty.chiba-u.jp.
J Affect Disord ; 290: 61-64, 2021 07 01.
Article em En | MEDLINE | ID: mdl-33993081
BACKGROUND: Brain-derived neurotrophic factor (BDNF) antisense RNA (BDNF-AS) was identified as naturally conserved non-coding antisense RNA that suppresses the transcription of BDNF. METHODS: We measured the expression of BDNF mRNA and BDNF-AS mRNA in iPSC and NSC from bipolar disorder (BD) patients and healthy control subjects, and postmortem brain samples such as the corpus callosum, the Brodmann area (BA8), and BA46 from BD patients and age- and sex-matched controls. RESULTS: The expression of BDNF mRNA in iPSC from BD patients (n = 6) was significantly lower than that of control subjects (n = 4) although the expression of BDNF mRNA in NSC from BD patients was significantly higher than that of control subjects. In contrast, there were no changes in the expression of BDNF-AS mRNA in both iPSC and NSC between two groups. The expression of BDNF mRNA in the BA46 from BD patients (n = 35) was significantly lower than that of controls (n = 34) although the expression of BDNF mRNA in the corpus callosum and BA8 was not different between two groups (n = 15). In contrast, there were no changes in expression of BDNF-AS mRNA in the three brain regions between two groups. Interestingly, there were significant positive correlations between BDNF mRNA expression and BDNF-AS mRNA expression in the postmortem brain samples. LIMITATIONS: Sample sizes are relatively low. CONCLUSIONS: Our data suggest that abnormalities in the expression of BDNF, but not BDNF-AS, play a role in the pathogenesis of BD.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Transtorno Bipolar / Células-Tronco Pluripotentes Induzidas / Células-Tronco Neurais Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Transtorno Bipolar / Células-Tronco Pluripotentes Induzidas / Células-Tronco Neurais Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article