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Journal ArticleDOI

Ontogeny and homeostasis of CNS myeloid cells.

Marco Prinz, +2 more
- 01 Apr 2017 - 
- Vol. 18, Iss: 4, pp 385-392
TLDR
Studies using cell-specific targeting, in vivo imaging, single-cell expression analysis and other sophisticated tools have increased the depth of knowledge of this immune-cell compartment and call for reevaluation of the traditional views on the origin, fate and function of distinct CNS myeloid subsets.
Abstract
Myeloid cells in the central nervous system (CNS) represent a heterogeneous class of innate immune cells that contribute to the maintenance of tissue homeostasis differentially during development and adulthood. The subsets of CNS myeloid cells identified so far, including parenchymal microglia and non-parenchymal meningeal, perivascular and choroid-plexus macrophages, as well as disease-associated monocytes, have classically been distinguished on the basis of their surface epitope expression, localization and morphology. However, studies using cell-specific targeting, in vivo imaging, single-cell expression analysis and other sophisticated tools have now increased the depth of knowledge of this immune-cell compartment and call for reevaluation of the traditional views on the origin, fate and function of distinct CNS myeloid subsets. The concepts of CNS macrophage biology that are emerging from these new insights have broad implications for the understanding and treatment of CNS diseases.

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Citations
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The Neurovascular Unit Coming of Age: A Journey through Neurovascular Coupling in Health and Disease

TL;DR: Evidence supports a conceptual shift in the mechanisms of neurovascular coupling, from a unidimensional process involving neuronal-astrocytic signaling to local blood vessels to a multidimensional one in which mediators released from multiple cells engage distinct signaling pathways and effector systems across the entire cerebrovascular network in a highly orchestrated manner.
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TL;DR: The current knowledge of how and where brain macrophages are generated is reviewed, with a focus on parenchymal microglia and their normal functions during development and homeostasis are discussed.
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Microglia Biology: One Century of Evolving Concepts.

TL;DR: Progress in imaging and genetics and the advent of single-cell technologies provided new insights into the much more complex and fascinating biology of microglia, and their functions in health and disease were better defined.
References
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Journal ArticleDOI

P2Y12 receptor is expressed on human microglia under physiological conditions throughout development and is sensitive to neuroinflammatory diseases.

TL;DR: The results suggest that P2Y12 is a useful marker for the identification of human microglia throughout the lifespan, and might help to discriminate activated microglial and infiltrating myeloid cells from quiescent microglian cells in the human CNS.
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Microglial cells are a component of the perivascular glia limitans.

TL;DR: The ultrastructural relation between microglial cells and cerebral blood vessels was studied in rat brains by immune electron microscopy and suggests that microglia cells may play an important role in antigen recognition at the blood‐brain barrier.
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Involvement of specific macrophage-lineage cells surrounding arterioles in barrier and scavenger function in brain cortex.

TL;DR: It is reported that specific cells surrounding arterioles, known as Mato's fluorescent granular perithelial (FGP) cells or perivascular microglial cells, contribute to the barrier function.
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