Transcriptional glucocorticoid effects in the brain: Finding the relevant target genes.
Onno C MeijerJacobus C BuurstedeEva M G VihoJorge Miguel AmayaAnne-Sophie C A M KoningMerel van der MeulenLisa T C M van WeertSusana N PaulJan KroonLisa L KoorneefPublished in: Journal of neuroendocrinology (2022)
Glucocorticoids are powerful modulators of brain function. They act via mineralocorticoid and glucocorticoid receptors (MR and GR). These are best understood as transcription factors. Although many glucocorticoid effects depend on the modulation of gene transcription, it is a major challenge to link gene expression to function given the large-scale, apparently pleiotropic genomic responses. The extensive sets of MR and GR target genes are highly specific per cell type, and the brain contains many different (neuronal and non-neuronal) cell types. Next to the set "trait" of cellular context, the "state" of other active signaling pathways will affect MR and GR transcriptional activity. Here, we discuss receptor specificity and contextual factors that determine the transcriptional outcome of MR/GR signaling, experimental possibilities offered by single-cell transcriptomics approaches, and reflect on how to make sense of lists of target genes in relation to understanding the functional effects of steroid receptor activation.
Keyphrases
- transcription factor
- genome wide identification
- gene expression
- single cell
- genome wide
- cerebral ischemia
- contrast enhanced
- resting state
- dna methylation
- white matter
- magnetic resonance
- rna seq
- copy number
- bioinformatics analysis
- functional connectivity
- high throughput
- dna binding
- genome wide analysis
- small molecule
- stem cells
- cell therapy
- cell proliferation
- binding protein
- blood brain barrier
- endoplasmic reticulum stress
- epithelial mesenchymal transition
- pi k akt
- induced apoptosis