Cross-Talk and Subset Control of Microglia and Associated Myeloid Cells in Neurological Disorders

Neurological disorders are highly prevalent and often lead to chronic debilitating disease. Neuroinflammation is a major driver across the spectrum of disorders, and microglia are key mediators of this response, gaining wide acceptance as a druggable cell target. Moreover, clinical providers have li...

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Main Authors: Jatia Mills, Liliana Ladner, Eman Soliman, John Leonard, Paul D. Morton, Michelle H. Theus
Format: Article
Language:English
Published: MDPI AG 2022-10-01
Series:Cells
Subjects:
Online Access:https://www.mdpi.com/2073-4409/11/21/3364
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author Jatia Mills
Liliana Ladner
Eman Soliman
John Leonard
Paul D. Morton
Michelle H. Theus
author_facet Jatia Mills
Liliana Ladner
Eman Soliman
John Leonard
Paul D. Morton
Michelle H. Theus
author_sort Jatia Mills
collection DOAJ
description Neurological disorders are highly prevalent and often lead to chronic debilitating disease. Neuroinflammation is a major driver across the spectrum of disorders, and microglia are key mediators of this response, gaining wide acceptance as a druggable cell target. Moreover, clinical providers have limited ability to objectively quantify patient-specific changes in microglia status, which can be a predictor of illness and recovery. This necessitates the development of diagnostic biomarkers and imaging techniques to monitor microglia-mediated neuroinflammation in coordination with neurological outcomes. New insights into the polarization status of microglia have shed light on the regulation of disease progression and helped identify a modifiable target for therapeutics. Thus, the detection and monitoring of microglia activation through the inclusion of diagnostic biomarkers and imaging techniques will provide clinical tools to aid our understanding of the neurologic sequelae and improve long-term clinical care for patients. Recent achievements demonstrated by pre-clinical studies, using novel depletion and cell-targeted approaches as well as single-cell RNAseq, underscore the mechanistic players that coordinate microglial activation status and offer a future avenue for therapeutic intervention.
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spelling doaj.art-40024302ae7942eca84128613438531d2023-11-24T04:07:28ZengMDPI AGCells2073-44092022-10-011121336410.3390/cells11213364Cross-Talk and Subset Control of Microglia and Associated Myeloid Cells in Neurological DisordersJatia Mills0Liliana Ladner1Eman Soliman2John Leonard3Paul D. Morton4Michelle H. Theus5Department of Biomedical Sciences and Pathobiology, Virginia Tech, Blacksburg, VA 24061, USAVirginia Tech Carilion School of Medicine, Roanoke, VA 24016, USADepartment of Biomedical Sciences and Pathobiology, Virginia Tech, Blacksburg, VA 24061, USADepartment of Biomedical Sciences and Pathobiology, Virginia Tech, Blacksburg, VA 24061, USADepartment of Biomedical Sciences and Pathobiology, Virginia Tech, Blacksburg, VA 24061, USADepartment of Biomedical Sciences and Pathobiology, Virginia Tech, Blacksburg, VA 24061, USANeurological disorders are highly prevalent and often lead to chronic debilitating disease. Neuroinflammation is a major driver across the spectrum of disorders, and microglia are key mediators of this response, gaining wide acceptance as a druggable cell target. Moreover, clinical providers have limited ability to objectively quantify patient-specific changes in microglia status, which can be a predictor of illness and recovery. This necessitates the development of diagnostic biomarkers and imaging techniques to monitor microglia-mediated neuroinflammation in coordination with neurological outcomes. New insights into the polarization status of microglia have shed light on the regulation of disease progression and helped identify a modifiable target for therapeutics. Thus, the detection and monitoring of microglia activation through the inclusion of diagnostic biomarkers and imaging techniques will provide clinical tools to aid our understanding of the neurologic sequelae and improve long-term clinical care for patients. Recent achievements demonstrated by pre-clinical studies, using novel depletion and cell-targeted approaches as well as single-cell RNAseq, underscore the mechanistic players that coordinate microglial activation status and offer a future avenue for therapeutic intervention.https://www.mdpi.com/2073-4409/11/21/3364single-cell sequencingcirculating monocytesmacrophagesneuroinflammationneurological diseasebone marrow transplant
spellingShingle Jatia Mills
Liliana Ladner
Eman Soliman
John Leonard
Paul D. Morton
Michelle H. Theus
Cross-Talk and Subset Control of Microglia and Associated Myeloid Cells in Neurological Disorders
Cells
single-cell sequencing
circulating monocytes
macrophages
neuroinflammation
neurological disease
bone marrow transplant
title Cross-Talk and Subset Control of Microglia and Associated Myeloid Cells in Neurological Disorders
title_full Cross-Talk and Subset Control of Microglia and Associated Myeloid Cells in Neurological Disorders
title_fullStr Cross-Talk and Subset Control of Microglia and Associated Myeloid Cells in Neurological Disorders
title_full_unstemmed Cross-Talk and Subset Control of Microglia and Associated Myeloid Cells in Neurological Disorders
title_short Cross-Talk and Subset Control of Microglia and Associated Myeloid Cells in Neurological Disorders
title_sort cross talk and subset control of microglia and associated myeloid cells in neurological disorders
topic single-cell sequencing
circulating monocytes
macrophages
neuroinflammation
neurological disease
bone marrow transplant
url https://www.mdpi.com/2073-4409/11/21/3364
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