Established and emerging techniques for the study of microglia: visualization, depletion, and fate mapping

Front Cell Neurosci. 2024 Feb 15:18:1317125. doi: 10.3389/fncel.2024.1317125. eCollection 2024.

Abstract

The central nervous system (CNS) is an essential hub for neuronal communication. As a major component of the CNS, glial cells are vital in the maintenance and regulation of neuronal network dynamics. Research on microglia, the resident innate immune cells of the CNS, has advanced considerably in recent years, and our understanding of their diverse functions continues to grow. Microglia play critical roles in the formation and regulation of neuronal synapses, myelination, responses to injury, neurogenesis, inflammation, and many other physiological processes. In parallel with advances in microglial biology, cutting-edge techniques for the characterization of microglial properties have emerged with increasing depth and precision. Labeling tools and reporter models are important for the study of microglial morphology, ultrastructure, and dynamics, but also for microglial isolation, which is required to glean key phenotypic information through single-cell transcriptomics and other emerging approaches. Strategies for selective microglial depletion and modulation can provide novel insights into microglia-targeted treatment strategies in models of neuropsychiatric and neurodegenerative conditions, cancer, and autoimmunity. Finally, fate mapping has emerged as an important tool to answer fundamental questions about microglial biology, including their origin, migration, and proliferation throughout the lifetime of an organism. This review aims to provide a comprehensive discussion of these established and emerging techniques, with applications to the study of microglia in development, homeostasis, and CNS pathologies.

Keywords: Cre/lox systems; electron microscopy; fate mapping; microglia; microglial depletion; microglial markers; positron emission tomography; reporter genes.

Publication types

  • Review

Grants and funding

The authors declare financial support was received for the research, authorship, and/or publication of this article. This work was carried out with the aid of a grant from the International Development Research Centre (IDRC; project ID 109925). BB was supported by a master award from the Division of Medical Sciences at University of Victoria. TH was supported by a British Columbia Children’s Hospital Research Institute Doctoral Award and the University of British Columbia MD/Ph.D. program. MC was supported by a doctoral training award from Fonds de Recherche du Québec–Santé. This work was supported by research grants from CIHR awarded to M-ÈT., who was a College Member of the Royal Society of Canada and a Canada Research Chair (Tier II) in Neurobiology of Aging and Cognition.