Advances in proteomic phenotyping of microglia in neurodegeneration

Microglia are dynamic resident immune cells of the central nervous system (CNS) that sense, survey, and respond to changes in their environment. In disease states, microglia transform from homeostatic to diverse molecular phenotypic states that play complex and causal roles in neurologic disease pat...

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Published inProteomics (Weinheim) Vol. 23; no. 13-14; pp. e2200183 - n/a
Main Authors Sunna, Sydney, Bowen, Christine A., Ramelow, Christina C., Santiago, Juliet V., Kumar, Prateek, Rangaraju, Srikant
Format Journal Article
LanguageEnglish
Published Germany Wiley Subscription Services, Inc 01.07.2023
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Summary:Microglia are dynamic resident immune cells of the central nervous system (CNS) that sense, survey, and respond to changes in their environment. In disease states, microglia transform from homeostatic to diverse molecular phenotypic states that play complex and causal roles in neurologic disease pathogenesis, as evidenced by the identification of microglial genes as genetic risk factors for neurodegenerative disease. While advances in transcriptomic profiling of microglia from the CNS of humans and animal models have provided transformative insights, the transcriptome is only modestly reflective of the proteome. Proteomic profiling of microglia is therefore more likely to provide functionally and therapeutically relevant targets. In this review, we discuss molecular insights gained from transcriptomic studies of microglia in the context of Alzheimer's disease as a prototypic neurodegenerative disease, and highlight existing and emerging approaches for proteomic profiling of microglia derived from in vivo model systems and human brain.
Bibliography:Srikant Rangaraju is senior author.
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ISSN:1615-9853
1615-9861
DOI:10.1002/pmic.202200183