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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

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Microglia and macrophages in brain homeostasis and disease

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

Selective targeting of perivascular macrophages for clearance of β-amyloid in cerebral amyloid angiopathy

TL;DR: The role of perivascular macrophages in regulating CAA severity in the TgCRND8 mouse model of AD is investigated and it is suggested that selective targeting of perIV vascular macrophage activation might constitute a therapeutic strategy to clear vascular amyloid.
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TMEM119 marks a subset of microglia in the human brain

TL;DR: Results suggest that TMEM119 serves as a reliable microglial marker that discriminates resident microglia from blood‐derived macrophages in the human brain.
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Distinct and Non-Redundant Roles of Microglia and Myeloid Subsets in Mouse Models of Alzheimer's Disease

TL;DR: Together, the data advocate selective functions of CCR2-expressing myeloid subsets, which could be targeted specifically to modify disease burden in AD.
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Myelomonocytic cell recruitment causes fatal CNS vascular injury during acute viral meningitis

TL;DR: It is concluded that a CD8+ T- cell-dependent disorder can proceed in the absence of direct T-cell effector mechanisms and rely instead on CTL-recruited myelomonocytic cells.
Journal ArticleDOI

Expression of Ia antigen on perivascular and microglial cells after sublethal and lethal motor neuron injury.

TL;DR: The existence of a population of immunocompetent perivascular cells normally present in adult rat brain that can be stimulated to express Ia antigen and a subpopulation of ramified microglia that arises through transformation of Ia-positive periv vascular cells in the adult under pathological conditions are proposed.
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