Semaphorin and plexin gene expression is altered in the prefrontal cortex of schizophrenia patients with and without auditory hallucinations

• Published in: Psychiatry research Vol. 229; no. 3; pp. 850 - 857
• Main Authors: Gilabert-Juan, Javier, Sáez, Ana Rosa, Lopez-Campos, Guillermo, Sebastiá-Ortega, Noelia, González-Martínez, Rocio, Costa, Juan, Haro, Josep María, Callado, Luis F, Meana, J. Javier, Nacher, Juán, Sanjuán, Julio, Moltó, María Dolores
• Format: Journal Article
• Language: English
• Published: Ireland Elsevier Ireland Ltd 30.10.2015
• Subjects: Adult; Aged; Aged, 80 and over; Auditory hallucinations; Axons; Brain - physiopathology; Cell Adhesion Molecules - genetics; Cell Adhesion Molecules - metabolism; Down-Regulation; Gene expression; Gene Expression Profiling; Hallucinations - genetics; Hallucinations - psychology; Humans; Middle Aged; Nerve Tissue Proteins - genetics; Nerve Tissue Proteins - metabolism; Neuronal Plasticity - genetics; Oligonucleotide Array Sequence Analysis; Plexins; Prefrontal cortex; Prefrontal Cortex - metabolism; Psychiatry; RNA, Messenger - metabolism; Schizophrenia; Schizophrenia - complications; Schizophrenia - genetics; Semaphorins; Semaphorins - genetics; Semaphorins - metabolism; Schizophrenia; Auditory hallucinations; Plexins; Prefrontal cortex; Gene expression; Semaphorins
• ISSN: 0165-1781; 1872-7123
• DOI: 10.1016/j.psychres.2015.07.074

Abstract Auditory hallucinations (AH) are clinical hallmarks of schizophrenia, however little is known about molecular genetics of these symptoms. In this study, gene expression profiling of postmortem brain samples from prefrontal cortex of schizophrenic patients without AH (SNA), patients with AH (SA) and control subjects were compared. Genome-wide expression analysis was conducted using samples of three individuals of each group and the Affymetrix GeneChip Human-Gene 1.0 ST-Array. This analysis identified the Axon Guidance pathway as one of the most differentially expressed network among SNA, SA and CNT. To confirm the transcriptome results, mRNA level quantification of seventeen genes involved in this pathway was performed in a larger sample. PLXNB1, SEMA3A, SEMA4D and SEM6C were upregulated in SNA or SA patients compared to controls. PLXNA1 and SEMA3D showed down-regulation in their expression in the patient’s samples, but differences remained statistically significant between the SNA patients and controls. Differences between SNA and SA were found in PLXNB1 expression which is decreased in SA patients. This study strengthens the contribution of brain plasticity in pathophysiology of schizophrenia and shows that non-hallucinatory patients present more alterations in frontal regions than patients with hallucinations concerning neural plasticity.