Gene expression changes in the brain of a Cushing's syndrome mouse model

被引:11
作者
Amaya, Jorge Miguel [1 ]
Viho, Eva M. G. [1 ]
Sips, Hetty C. M. [1 ]
Lalai, Reshma A. [1 ]
Sahut-Barnola, Isabelle [2 ]
Dumontet, Typhanie [2 ]
Montanier, Nathanaelle [2 ]
Pereira, Alberto M. [1 ]
Martinez, Antoine [2 ]
Meijer, Onno C. [1 ]
机构
[1] Leiden Univ, Med Ctr, Div Endocrinol, Dept Internal Med, Leiden, Netherlands
[2] Univ Clermont Auvergne, CNRS, INSERM, Genet Reprod & Dev, Clermont Ferrand, France
关键词
brain; Cushing's syndrome; glia; glucocorticoid; neuron; GLUCOCORTICOID-RECEPTOR GENE; TRANSCRIPTOMIC CELL-TYPES; LONG-TERM REMISSION; STRESS-LIKE LEVELS; MESSENGER-RNA; CORTICOSTERONE; OLIGODENDROCYTE; MICROGLIA; HIPPOCAMPUS; SYMPTOMS;
D O I
10.1111/jne.13125
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Excess glucocorticoid exposure affects emotional and cognitive brain functions. The extreme form, Cushing's syndrome, is adequately modelled in the AdKO(2.0) mouse, consequential to adrenocortical hypertrophy and hypercorticosteronemia. We previously reported that the AdKO(2.0) mouse brain undergoes volumetric changes that resemble closely those of Cushing's syndrome human patients, as well as changes in expression of glial related marker proteins. In the present work, the expression of genes related to glial and neuronal cell populations and functions was assessed in regions of the anterior brain, hippocampus, amygdala and hypothalamus. Glucocorticoid target genes were consistently regulated, including CRH mRNA suppression in the hypothalamus and induction in amygdala and hippocampus, even if glucocorticoid receptor protein was downregulated. Expression of glial genes was also affected in the AdKO(2.0) mouse brain, indicating a different activation status in glial cells. Generic markers for neuronal cell populations, and cellular integrity were only slightly affected. Our findings highlight the vulnerability of glial cell populations to chronic high levels of circulating glucocorticoids.
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页数:16
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