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      Abnormal expression of cell recognition molecules in schizophrenia.

      Experimental Neurology
      Bipolar Disorder, metabolism, Cell Adhesion Molecules, Neuronal, biosynthesis, Hippocampus, Humans, Leukocyte L1 Antigen Complex, Membrane Glycoproteins, Middle Aged, Neural Cell Adhesion Molecules, Prefrontal Cortex, Reference Values, Schizophrenia, Suicide

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          Abstract

          Schizophrenia is a neuropsychiatric disorder of unknown etiology associated with subtle changes in brain morphology. The cell recognition molecules (CRMs) neural cell adhesion molecule (N-CAM) and L1 are involved in morphoregulatory events and numerous neurodevelopmental processes. We found a selective increase of 105- to 115-kDa N-CAM in the hippocampus and prefrontal cortex of patients with schizophrenia while other N-CAM isoforms and L1 proteins were not altered. There was also evidence for an abnormality in CRM expression in schizophrenic patients: concentrations of 200-kDa L1 were strongly correlated with expression of N-CAM isoforms and cleaved L1 proteins in controls, whereas these correlations were absent in patients with schizophrenia. The increase of the 105- to 115-kDa N-CAM isoform in the brains of patients with schizophrenia confirms previous cerebrospinal fluid findings. Increased N-CAM in schizophrenia may result from structural brain abnormalities, from glial processing of N-CAM, or from an aberration in the regulation of N-CAM expression.

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