Evidence of microglial involvement in the childhood abuse-associated increase in perineuronal nets in the ventromedial prefrontal cortex

被引:0
|
作者
Belliveau, Claudia [1 ,2 ]
Rahimian, Reza [1 ]
Fakhfouri, Gohar [3 ]
Hosdey, Clementine
Simard, Sophie [1 ,2 ]
Davoli, Maria Antonietta [1 ]
Mirault, Dominique [1 ]
Giros, Bruno [2 ,3 ]
Turecki, Gustavo [1 ,2 ,3 ]
Mechawar, Naguib [1 ,2 ,3 ]
机构
[1] McGill Univ, Douglas Mental Hlth Univ Inst, McGill Grp Suicide Studies, Montreal, PQ, Canada
[2] McGill Univ, Integrated Program Neurosci, Montreal, PQ, Canada
[3] McGill Univ, Dept Psychiat, Montreal, PQ, Canada
关键词
Humans; Adverse Childhood Experiences; Microglia; Extracellular Matrix; Matrix Metalloproteinase 9; EXTRACELLULAR-MATRIX; MESSENGER-RNA; TRANSCRIPTOME; TRANSLATION; FRACTALKINE; DEFICIENCY; DEPRESSION; SYNAPSES; MATTER; GLIA;
D O I
10.1016/j.bbi.2024.12.013
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Microglia, known for their diverse roles in the central nervous system, have recently been recognized for their involvement in degrading the extracellular matrix. Perineuronal nets (PNNs), a specialized form of this matrix, are crucial for stabilizing neuronal connections and constraining plasticity. Our group recently reported increased PNN densities in the ventromedial prefrontal cortex (vmPFC) of depressed individuals that died by suicide in adulthood after experiencing childhood abuse (DS-CA) compared to matched controls. To explore potential underlying mechanisms, we employed a comprehensive approach in similar postmortem vmPFC samples, combining a human matrix metalloproteinase and chemokine array, isolation of CD11b-positive microglia and enzyme-linked immunosorbent assays (ELISA). Our findings indicate a significant downregulation of matrix metalloproteinase (MMP)-9 and tissue inhibitors of metalloproteinases (TIMP)-2 in both whole vmPFC grey matter and isolated microglial cells from DS-CA samples. Furthermore, our experiments reveal that a history of child abuse is associated with diminished levels of microglial CX3CR1 and IL33R in both vmPFC whole lysate and CD11b+ isolated cells. However, levels of the CX3CR1 ligand, CX3CL1 (Fractalkine), did not differ between groups. While these data suggest potential long-lasting alterations in microglial markers in the vmPFC of individuals exposed to severe childhood adversity, direct functional assessments were not conducted. Nonetheless, these findings offer insight into how childhood abuse may contribute to PNN alterations via microglial-related mechanisms.
引用
收藏
页码:321 / 334
页数:14
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