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Reduction in Reelin immunoreactivity in hippocampus of subjects with schizophrenia, bipolar disorder and major depression

Abstract

Accumulation of neurobiological knowledge points to neurodevelopmental origins for certain psychotic and mood disorders. Recent landmark postmortem reports implicate Reelin, a secretory glycoprotein responsible for normal lamination of brain, in the pathology of schizophrenia and bipolar disorders. We employed quantitative immunocytochemistry to measure levels of Reelin protein in various compartments of hippocampal formation in subjects diagnosed with schizophrenia, bipolar disorder and major depression compared to normal controls. Significant reductions were observed in Reelin-positive adjusted cell densities in the dentate molecular layer (ANOVA, P < 0.001), CA4 area (ANOVA, P < 0.001), total hippocampal area (ANOVA, P < 0.038) and in Reelin-positive cell counts in CA4 (ANOVA, P < 0.042) of schizophrenics vs controls. Adjusted Reelin-positive cell densities were also reduced in CA4 areas of subjects with bipolar disorder (ANOVA, P < 0.001) and nonsignificantly in those with major depression. CA4 areas were also significantly reduced in schizophrenic (ANOVA, P < 0.009) patients. No significant effects of confounding variables were found. The exception was that family history of psychiatric illness correlated strongly with Reelin reductions in several areas of hippocampus (CA4, adjusted cell density, F = 13.77, P = 0.001). We present new immunocytochemical evidence showing reductions in Reelin expression in hippocampus of subjects with schizophrenia, bipolar disorder and major depression and confirm recent reports documenting a similar deficit involving Reelin expression in brains of subjects with schizophrenia and bipolar disorder.

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References

  1. D'Arcangelo G, Nakajima K, Miyata T, Ogawa M, Mikoshiba K, Curran T . Reelin is a secreted glycoprotein recognized by the CR-50 monoclonal antibody J Neurosci 1997; 17: 23–31

    Article  CAS  Google Scholar 

  2. Bar I, Lambert de Rouvroit C, Royaux I, Krizman DB, Dernancourt C, Ruelle D et al. A YAC contig containing the reeler locus with preliminary characterization of candidate gene fragments Genomics 1995; 26: 543–549

    Article  CAS  Google Scholar 

  3. D'Arcangelo G, Miao GG, Chen S-C, Soares HD, Morgan JI, Curran T . A protein related to extracellular matrix proteins deleted in the mouse mutant reeler Nature 1995; 374: 719–723

    Article  CAS  Google Scholar 

  4. Klar A, Baldassare M, Jessell TM . F-Spondin: a gene expressed at high levels in the floor plate encodes a secreted protein that promotes neural cell adhesion and neurite extension Cell 1992; 69: 95–110

    Article  CAS  Google Scholar 

  5. Vrucinic N, Chiquet-Ehrismann RR . Tenascin function and regulation of expression Symp Soc Exp Biol 1993; 47: 155–162

    Google Scholar 

  6. Goffinet AM . An early developmental defect in the cerebral cortex of the Reeler mouse Anat Embryol 1979; 157: 205–216

    Article  CAS  Google Scholar 

  7. Ogawa M, Miyata T, Nakajima K, Yagyu K, Seike M, Ikenaka K et al. The reeler gene-associated antigen on Cajal–Retzius neurons is a crucial molecule for laminar organization of cortical neurons Neuron 1995; 14: 899–912

    Article  CAS  Google Scholar 

  8. Borrell V, Del Rio JA, Alcantra S, Derer M, Martinez A, D'Arcangelo G et al. Reelin regulates entorhino-hippocampal connections J Neurosci 1999; 19: 1345–1358

    Article  CAS  Google Scholar 

  9. Rodriguez MA, Pesold C, Liu WS, Kriho V, Guidotti A, Pappas GD et al. Colocalization of integrin receptors and Reelin in dendritic spine post-synaptic densities of adult non-human primate cortex Proc Natl Acad Sci 2000; 97: 3550–3555

    Article  CAS  Google Scholar 

  10. Impagnatiello F, Guidotti A, Pesold C, Dwlivedi Y, Caruncho H, Pisu MG et al. A decrease of Reelin expression as a putative vulnerability factor in schizophrenia Proc Natl Acad Sci 1998; 95: 15718–15723

    Article  CAS  Google Scholar 

  11. Smallheiser NR, Costa E, Guidotti A, Impagnatiello F, Auta J, Lacor P et al. Expression of Reelin in adult mammalian blood, liver, pituitary pars intermedia, and adrenal chromaffin cells Proc Natl Acad Sci 2000; 97: 1281–1286

    Article  Google Scholar 

  12. Guidotti A, Auta J, Davis J, Dwivedi Y, Grayson D, Impagnatiello F et al. Decrease in Reelin and glutamic acid decarboxylase 67 (GAD67) expression in schizophrenia and bipolar disorder: a postmortem brain study Arch Gen Psychiatry 2000; (in press

  13. Knable MB, Fuller Torrey E, Webster MJ, Bartko JJ . Multivariate analysis of prefrontal cortical data from the Stanley Foundation Neuropathology Consortium Brain Res Bull 2000; (in press

  14. Akbarian S, Bunney Jr WE, Potkin SG, Wigal SB, Hagman JO, Sandman ET et al. Altered distribution of nicotinamide-adenine dinucleotide phosphate-diaphorase cells in frontal lobe of schizophrenics implies disturbances of cortical development Arch Gen Psychiatry 1993; 50: 169–177

    Article  CAS  Google Scholar 

  15. Akbarian S, Vinuela A, Kim JJ, Potkin SG, Bunney WE, Jones EG . Distorted distribution of nicotinamide-adenine dinucleotide phosphate-diaphorase neurons in temporal lobe of schizophrenics implies anomalous cortical development Arch Gen Psychiatry 1993; 50: 178–187

    Article  CAS  Google Scholar 

  16. Fuller Torrey E, Webster M, Knable M, Johnston N, Yolken RH . The Stanley Foundation brain collection and Neuropathology Consortium Schizophr Res 2000; 44: 151–155

    Article  Google Scholar 

  17. Pesold C, Impagnatiello F, Pisu MG, Uzunov DP, Costa E, Guidotti A et al. Reelin is preferentially expressed in neurons synthesizing gamma-amniobutyric acid in cortex and hippocampus of adult rats Proc Natl Acad Sci 1998; 95: 3221–3226

    Article  CAS  Google Scholar 

  18. De Bergeyck V, Nakajima K, Lambert de Roubroit C, Naerhuyzen B, Goffinet AM, Miyata T et al. A truncated Reelin protein is produced but not secreted in the ‘Orleans’ reeler mutation (Reln rl-crl) Mol Brain Res 1997; 50: 85–90

    Article  CAS  Google Scholar 

  19. Weinberger DR . Cell biology of the hippocampal formation in schizophrenia Biol Psychiatry 1999; 45: 395–402

    Article  CAS  Google Scholar 

  20. Nakajima K, Mikoshiba K, Miyata T, Kudo C, Ogawa M . Disruption of hippocampal development in vivo by CR-50 mAb against Reelin Proc Natl Acad Sci 1997; 94: 8196–8201

    Article  CAS  Google Scholar 

  21. Selemon LD, Goldman-Rakic PS . The reduced neuropil hypothesis: a circuit based model of schizophrenia Biol Psychiatry 1999; 45: 17–25

    Article  CAS  Google Scholar 

  22. Fatemi SH, Emamian ES, Kist D, Sidwell RW, Nakajima K, Akhter P et al. Defective corticogenesis and reduction in Reelin immunoreactivity in cortex and hippocampus of prenatally infected neonatal mice Mol Psychiatry 1999; 4: 145–154

    Article  CAS  Google Scholar 

  23. Tueting P, Costa E, Dwivedi Y, Guidotti A, Impagnatiello F, Manev R et al. The phenotypic characteristics of heterozygous reeler mouse Neuroreport 1999; 10: 1329–1334

    Article  CAS  Google Scholar 

  24. Suddath RL, Christison GW, Torrey EF, Casanova MF, Weinberger DR . Anatomical abnormalities in the brains of monozygotic twins discordant for schizophrenia N Engl J Med 1990; 322: 789–794

    Article  CAS  Google Scholar 

  25. Velakoulis D, Pantelis C, McGorry PD, Dudgeon P, Brewer W, Cook M et al. Hippocampal volume in first episode psychosis and chronic schizophrenia Arch Gen Psychiatry 1999; 56: 133–140

    Article  CAS  Google Scholar 

  26. Hoge EA, Friedman L, Schulz SC . Meta-analysis of brain size in bipolar disorder Schizophr Res 1999; 37: 177–181

    Article  CAS  Google Scholar 

  27. Mohn AR, Gainetdinov RR, Caron MG, Koller BH . Mice with reduced NMDA receptor expression display behaviors related to schizophrenia Cell 1999; 98: 427–436

    Article  CAS  Google Scholar 

  28. Trommsdorff M, Gotthardt M, Hiesberger T, Shelton J, Stockinger W, Nimpf J et al. Reeler/disabled-like disruption of neuronal migration in knockout mice lacking the VLDL receptor and ApoE receptor 2 Cell 1999; 97: 689–701

    Article  CAS  Google Scholar 

  29. Anton ES, Kreidberg JA, Rakic P . Distinct functions of α3 and αν integrin receptors in neuronal migration and laminar organization of the cerebral cortex Neuron 1999; 22: 277–289

    Article  CAS  Google Scholar 

  30. Lacor P, Grayson DR, Auta J, Sugaya I, Costa E, Guidotti A . Reelin secretion from glutamatergic neurons in culture is independent from neurotransmitter regulation Proc Natl Acad Sci 2000; 97: 3556–3561

    Article  CAS  Google Scholar 

  31. Akbarian S, Kim JJ, Potkin SG, Hagman JO, Tafazzoli A, Bunney WE et al. Gene expression for glutamic acid decarboxylase is reduced without loss of neurons in prefrontal cortex of schizophrenics Arch Gen Psychiatry 1995; 52: 258–266

    Article  CAS  Google Scholar 

  32. Volk DW, Austin MC, Pierri JN, Sampson AR, Lewis DA . Decreased glutamic acid decarboxylase 67 messenger RNA expression in a subset of prefrontal cortical gamma-aminobutyric acid neurons in subjects with schizophrenia Arch Gen Psychiatry 2000; 57: 237–245

    Article  CAS  Google Scholar 

Download references

Acknowledgements

Supported by Minnesota Medical Foundation and Stanley Foundation grants (SHF). We are grateful to Dr Andre M Goffinet for his generous gifts of G10 and 142 antibodies and to the Stanley Foundation Neuropathology Consortium Brain Bank for provision of brain samples courtesy of Drs LB Bigelow, J Cervenak, MM Herman, TN Hyde, JE Kleinman, M Knable, JD Paltan, RM Post, EF Torrey, MJ Webster and RH Yolken. We are indebted to Dr Joel Hektner for his astute statistical help with reanalysis of data. We appreciate the helpful comments provided by Drs E Costa, A Guidotti, C Pesold, SC Schulz and M Knable regarding this manuscript. We appreciate the secretarial assistance of Ms Janet Holland and Ms Heather Winstead, and careful review of data by Mr Joel Stary.

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Fatemi, S., Earle, J. & McMenomy, T. Reduction in Reelin immunoreactivity in hippocampus of subjects with schizophrenia, bipolar disorder and major depression. Mol Psychiatry 5, 654–663 (2000). https://doi.org/10.1038/sj.mp.4000783

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