Layer III pyramidal cells in the prefrontal cortex reveal morphological changes in subjects with depression, schizophrenia, and suicide

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Layer III pyramidal cells in the prefrontal cortex reveal morphological changes in subjects with depression, schizophrenia, and suicide. / Larsen, Nick Y.; Vihrs, Ninna; Møller, Jesper; Sporring, Jon; Tan, Xueke; Li, Xixia; Ji, Gang; Rajkowska, Grazyna; Sun, Fei; Nyengaard, Jens R.

In: Translational Psychiatry, Vol. 12, No. 1, 2022, p. 363.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Larsen, NY, Vihrs, N, Møller, J, Sporring, J, Tan, X, Li, X, Ji, G, Rajkowska, G, Sun, F & Nyengaard, JR 2022, 'Layer III pyramidal cells in the prefrontal cortex reveal morphological changes in subjects with depression, schizophrenia, and suicide', Translational Psychiatry, vol. 12, no. 1, pp. 363. https://doi.org/10.1038/s41398-022-02128-0

APA

Larsen, N. Y., Vihrs, N., Møller, J., Sporring, J., Tan, X., Li, X., Ji, G., Rajkowska, G., Sun, F., & Nyengaard, J. R. (2022). Layer III pyramidal cells in the prefrontal cortex reveal morphological changes in subjects with depression, schizophrenia, and suicide. Translational Psychiatry, 12(1), 363. https://doi.org/10.1038/s41398-022-02128-0

Vancouver

Larsen NY, Vihrs N, Møller J, Sporring J, Tan X, Li X et al. Layer III pyramidal cells in the prefrontal cortex reveal morphological changes in subjects with depression, schizophrenia, and suicide. Translational Psychiatry. 2022;12(1):363. https://doi.org/10.1038/s41398-022-02128-0

Author

Larsen, Nick Y. ; Vihrs, Ninna ; Møller, Jesper ; Sporring, Jon ; Tan, Xueke ; Li, Xixia ; Ji, Gang ; Rajkowska, Grazyna ; Sun, Fei ; Nyengaard, Jens R. / Layer III pyramidal cells in the prefrontal cortex reveal morphological changes in subjects with depression, schizophrenia, and suicide. In: Translational Psychiatry. 2022 ; Vol. 12, No. 1. pp. 363.

Bibtex

@article{b1a93bb91ac84d4f8504565df631b144,
title = "Layer III pyramidal cells in the prefrontal cortex reveal morphological changes in subjects with depression, schizophrenia, and suicide",
abstract = "Brodmann Area 46 (BA46) has long been regarded as a hotspot of disease pathology in individuals with schizophrenia (SCH) and major depressive disorder (MDD). Pyramidal neurons in layer III of the Brodmann Area 46 (BA46) project to other cortical regions and play a fundamental role in corticocortical and thalamocortical circuits. The AutoCUTS-LM pipeline was used to study the 3-dimensional structural morphology and spatial organization of pyramidal cells. Using quantitative light microscopy, we used stereology to calculate the entire volume of layer III in BA46 and the total number and density of pyramidal cells. Volume tensors estimated by the planar rotator quantified the volume, shape, and nucleus displacement of pyramidal cells. All of these assessments were carried out in four groups of subjects: controls (C, n = 10), SCH (n = 10), MDD (n = 8), and suicide subjects with a history of depression (SU, n = 11). SCH subjects had a significantly lower somal volume, total number, and density of pyramidal neurons when compared to C and tended to show a volume reduction in layer III of BA46. When comparing MDD subjects with C, the measured parameters were inclined to follow SCH, although there was only a significant reduction in pyramidal total cell number. While no morphometric differences were observed between SU and MDD, SU had a significantly higher total number of pyramidal cells and nucleus displacement than SCH. Finally, no differences in the spatial organization of pyramidal cells were found among groups. These results suggest that despite significant morphological alterations in layer III of BA46, which may impair prefrontal connections in people with SCH and MDD, the spatial organization of pyramidal cells remains the same across the four groups and suggests no defects in neuronal migration. The increased understanding of pyramidal cell biology may provide the cellular basis for symptoms and neuroimaging observations in SCH and MDD patients.",
author = "Larsen, {Nick Y.} and Ninna Vihrs and Jesper M{\o}ller and Jon Sporring and Xueke Tan and Xixia Li and Gang Ji and Grazyna Rajkowska and Fei Sun and Nyengaard, {Jens R.}",
note = "Publisher Copyright: {\textcopyright} 2022. The Author(s).",
year = "2022",
doi = "10.1038/s41398-022-02128-0",
language = "English",
volume = "12",
pages = "363",
journal = "Translational Psychiatry",
issn = "2158-3188",
publisher = "nature publishing group",
number = "1",

}

RIS

TY - JOUR

T1 - Layer III pyramidal cells in the prefrontal cortex reveal morphological changes in subjects with depression, schizophrenia, and suicide

AU - Larsen, Nick Y.

AU - Vihrs, Ninna

AU - Møller, Jesper

AU - Sporring, Jon

AU - Tan, Xueke

AU - Li, Xixia

AU - Ji, Gang

AU - Rajkowska, Grazyna

AU - Sun, Fei

AU - Nyengaard, Jens R.

N1 - Publisher Copyright: © 2022. The Author(s).

PY - 2022

Y1 - 2022

N2 - Brodmann Area 46 (BA46) has long been regarded as a hotspot of disease pathology in individuals with schizophrenia (SCH) and major depressive disorder (MDD). Pyramidal neurons in layer III of the Brodmann Area 46 (BA46) project to other cortical regions and play a fundamental role in corticocortical and thalamocortical circuits. The AutoCUTS-LM pipeline was used to study the 3-dimensional structural morphology and spatial organization of pyramidal cells. Using quantitative light microscopy, we used stereology to calculate the entire volume of layer III in BA46 and the total number and density of pyramidal cells. Volume tensors estimated by the planar rotator quantified the volume, shape, and nucleus displacement of pyramidal cells. All of these assessments were carried out in four groups of subjects: controls (C, n = 10), SCH (n = 10), MDD (n = 8), and suicide subjects with a history of depression (SU, n = 11). SCH subjects had a significantly lower somal volume, total number, and density of pyramidal neurons when compared to C and tended to show a volume reduction in layer III of BA46. When comparing MDD subjects with C, the measured parameters were inclined to follow SCH, although there was only a significant reduction in pyramidal total cell number. While no morphometric differences were observed between SU and MDD, SU had a significantly higher total number of pyramidal cells and nucleus displacement than SCH. Finally, no differences in the spatial organization of pyramidal cells were found among groups. These results suggest that despite significant morphological alterations in layer III of BA46, which may impair prefrontal connections in people with SCH and MDD, the spatial organization of pyramidal cells remains the same across the four groups and suggests no defects in neuronal migration. The increased understanding of pyramidal cell biology may provide the cellular basis for symptoms and neuroimaging observations in SCH and MDD patients.

AB - Brodmann Area 46 (BA46) has long been regarded as a hotspot of disease pathology in individuals with schizophrenia (SCH) and major depressive disorder (MDD). Pyramidal neurons in layer III of the Brodmann Area 46 (BA46) project to other cortical regions and play a fundamental role in corticocortical and thalamocortical circuits. The AutoCUTS-LM pipeline was used to study the 3-dimensional structural morphology and spatial organization of pyramidal cells. Using quantitative light microscopy, we used stereology to calculate the entire volume of layer III in BA46 and the total number and density of pyramidal cells. Volume tensors estimated by the planar rotator quantified the volume, shape, and nucleus displacement of pyramidal cells. All of these assessments were carried out in four groups of subjects: controls (C, n = 10), SCH (n = 10), MDD (n = 8), and suicide subjects with a history of depression (SU, n = 11). SCH subjects had a significantly lower somal volume, total number, and density of pyramidal neurons when compared to C and tended to show a volume reduction in layer III of BA46. When comparing MDD subjects with C, the measured parameters were inclined to follow SCH, although there was only a significant reduction in pyramidal total cell number. While no morphometric differences were observed between SU and MDD, SU had a significantly higher total number of pyramidal cells and nucleus displacement than SCH. Finally, no differences in the spatial organization of pyramidal cells were found among groups. These results suggest that despite significant morphological alterations in layer III of BA46, which may impair prefrontal connections in people with SCH and MDD, the spatial organization of pyramidal cells remains the same across the four groups and suggests no defects in neuronal migration. The increased understanding of pyramidal cell biology may provide the cellular basis for symptoms and neuroimaging observations in SCH and MDD patients.

UR - http://www.scopus.com/inward/record.url?scp=85137208708&partnerID=8YFLogxK

U2 - 10.1038/s41398-022-02128-0

DO - 10.1038/s41398-022-02128-0

M3 - Journal article

C2 - 36064829

AN - SCOPUS:85137208708

VL - 12

SP - 363

JO - Translational Psychiatry

JF - Translational Psychiatry

SN - 2158-3188

IS - 1

ER -

ID: 319248528