Essential contributions of enhancer genomic regulatory elements to microglial cell identity and functions.
André Machado XavierSarah BelhocineDavid GosselinPublished in: Wiley interdisciplinary reviews. Systems biology and medicine (2019)
Microglia are the specialized macrophages of the brain and play essential roles in ensuring its proper functioning. Accumulating evidence suggests that these cells coordinate the inflammatory response that accompanies various clinical brain conditions, including neurodegenerative diseases and psychiatric disorders. Therefore, investigating the functions of these cells and how these are regulated have become important areas of research in neuroscience over the past decade. In this regards, recent efforts to characterize the epigenomic mechanisms underlying microglial gene transcription have provided significant insights into the mechanisms that control the ontogeny and the cellular competences of microglia. In particular, these studies have established that a substantial proportion of the microglial repertoire of promoter-distal genomic regulatory elements, or enhancers, is relatively specific to these cells compared to other tissue-resident macrophages. Notably, this specificity is under the regulation of factors present in the brain that modulate activity of target axes of signaling pathways-transcription factors in microglia. Thus, the microglial enhancer repertoire is highly responsive to perturbations in the cerebral tissue microenvironment and this responsiveness has profound implications on the activity of these cells in brain diseases. This article is categorized under: Physiology > Mammalian Physiology in Health and Disease Models of Systems Properties and Processes > Mechanistic Models Biological Mechanisms > Cell Fates Developmental Biology > Lineages.
Keyphrases
- inflammatory response
- transcription factor
- induced apoptosis
- cell cycle arrest
- neuropathic pain
- lps induced
- lipopolysaccharide induced
- signaling pathway
- resting state
- stem cells
- endoplasmic reticulum stress
- white matter
- public health
- toll like receptor
- cerebral ischemia
- single cell
- cell death
- copy number
- gene expression
- risk assessment
- cell therapy
- genome wide
- spinal cord injury
- cell proliferation
- social media
- intellectual disability
- drug delivery
- functional connectivity
- quality improvement
- dna binding
- genome wide identification
- patient safety