Cortical thickness differences are associated with cellular component morphogenesis of astrocytes and excitatory neurons in nonsuicidal self-injuring youth

Author:

Cai Suping1ORCID,Guo Zitong1,Wang Xuwen1,Huang Kexin1,Yuan Kai1234567ORCID,Huang Liyu1ORCID

Affiliation:

1. School of Life Science and Technology, Xidian University , Xi’an, Shaanxi 710071 , PR China

2. School of Life Science andTechnology , Xidian University, , Xi'an, Shaanxi 710071 , PR China

3. Engineering Research Center of Molecular and Neuro Imaging Ministry of Education , Xidian University, , Xi'an, Shaanxi 710071 , PR China

4. Information Processing Laboratory , School of Information Engineering, , Baotou, Inner Mongolia 014010 , PR China

5. Inner Mongolia University of Science and Technology , School of Information Engineering, , Baotou, Inner Mongolia 014010 , PR China

6. Xi'an Key Laboratory of Intelligent Sensing and Regulation of Trans-Scale Life Information , School of Life Science and Technology, , Xi'an, Shaanxi 710126 , PR China

7. Xidian University , School of Life Science and Technology, , Xi'an, Shaanxi 710126 , PR China

Abstract

Abstract Nonsuicidal self-injury (NSSI) generally occurs in youth and probably progresses to suicide. An examination of cortical thickness differences (ΔCT) between NSSI individuals and controls is crucial to investigate potential neurobiological correlates. Notably, ΔCT are influenced by specific genetic factors, and a large proportion of cortical thinning is associated with the expression of genes that overlap in astrocytes and pyramidal cells. However, in NSSI youth, the mechanisms underlying the relations between the genetic and cell type-specific transcriptional signatures to ΔCT are unclear. Here, we studied the genetic association of ΔCT in NSSI youth by performing a partial least-squares regression (PLSR) analysis of gene expression data and 3D-T1 brain images of 45 NSSI youth and 75 controls. We extracted the top-10 Gene Ontology terms for the enrichment results of upregulated PLS component 1 genes related to ΔCT to conduct the cell-type classification and enrichment analysis. Enrichment of cell type-specific genes shows that cellular component morphogenesis of astrocytes and excitatory neurons accounts for the observed NSSI-specific ΔCT. We validated the main results in independent datasets to verify the robustness and specificity. We concluded that the brain ΔCT is associated with cellular component morphogenesis of astrocytes and excitatory neurons in NSSI youth.

Funder

National Natural Science Foundation of China

China Postdoctoral Science Foundation

National Natural Science Foundation of Shaanxi of China

Publisher

Oxford University Press (OUP)

Subject

Cellular and Molecular Neuroscience,Cognitive Neuroscience

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