Microglia are the resident immune cells of the central nervous system, playing a crucial role in monitoring and responding to changes in the brain environment. Traditionally, microglia have been classified into two broad categories based on their activation status - M1 and M2. M1 microglia are considered pro-inflammatory, while M2 microglia are seen as anti-inflammatory. However, it has become increasingly clear that this binary classification does not accurately capture the diverse and dynamic nature of microglial responses in the brain. Recent advancements in single-cell transcriptomics and imaging technologies have revealed that microglia are a highly heterogeneous population, with distinct subpopulations that can be identified based on their unique gene expression profiles and functional characteristics. These diverse and context-dependent responses highlight the complexity of microglial biology and challenge the simplistic M1/M2 classification. Instead of rigidly categorizing microglia into discrete groups, it is more appropriate to view their activation along a continuum, with a focus on their functional outcomes rather than predetermined classifications. This allows for a more nuanced understanding of microglial responses in different brain pathologies, and opens up new opportunities for developing targeted therapies that harness the beneficial functions of microglia while mitigating their potentially harmful effects.
In this Research Topic, we aim to bring together the latest findings on the diversity of microglia, with a focus on the molecular and cellular mechanisms that underlie their functional differences. By shedding light on the complexity of microglial subpopulations and their unique functions, we hope to provide a more comprehensive understanding of the role of microglia in brain health and disease. This knowledge could ultimately lead to the development of novel therapeutic strategies that target specific microglial subtypes, with the potential to improve outcomes for individuals with neurological conditions.
We welcome submissions on the following topics, but are not limited to:
- The significant contribution of microglia to brain development and their crucial role in maintaining brain function.
- The diverse functions of microglia including the elimination of excess synapses, generation of new neurons, and the formation of neural networks.
- The dynamic nature of microglia phenotypes and functions, which vary with time and location within the brain.
- The ability of microglia to change their phenotype and function to help control inflammation and promote healing after brain injuries.
- The intricate mechanisms involved in the alteration of genes and cell signals in microglia following brain injuries.
- The pivotal role of microglia in the post-injury cleanup of debris, the maintenance of the blood-brain barrier, and the promotion of neuronal growth.
- The impact of age and sex variations on the response of microglia after a brain injury.
- The potential benefits and complexities of therapeutically targeting microglia due to their multifaceted nature and the possibility of unintended side effects.
Keywords:
microglial, macrophages, phenotypical heterogeneity, functional heterogeneity, neurological disease, neuroinflammation
Important Note:
All contributions to this Research Topic must be within the scope of the section and journal to which they are submitted, as defined in their mission statements. Frontiers reserves the right to guide an out-of-scope manuscript to a more suitable section or journal at any stage of peer review.
Microglia are the resident immune cells of the central nervous system, playing a crucial role in monitoring and responding to changes in the brain environment. Traditionally, microglia have been classified into two broad categories based on their activation status - M1 and M2. M1 microglia are considered pro-inflammatory, while M2 microglia are seen as anti-inflammatory. However, it has become increasingly clear that this binary classification does not accurately capture the diverse and dynamic nature of microglial responses in the brain. Recent advancements in single-cell transcriptomics and imaging technologies have revealed that microglia are a highly heterogeneous population, with distinct subpopulations that can be identified based on their unique gene expression profiles and functional characteristics. These diverse and context-dependent responses highlight the complexity of microglial biology and challenge the simplistic M1/M2 classification. Instead of rigidly categorizing microglia into discrete groups, it is more appropriate to view their activation along a continuum, with a focus on their functional outcomes rather than predetermined classifications. This allows for a more nuanced understanding of microglial responses in different brain pathologies, and opens up new opportunities for developing targeted therapies that harness the beneficial functions of microglia while mitigating their potentially harmful effects.
In this Research Topic, we aim to bring together the latest findings on the diversity of microglia, with a focus on the molecular and cellular mechanisms that underlie their functional differences. By shedding light on the complexity of microglial subpopulations and their unique functions, we hope to provide a more comprehensive understanding of the role of microglia in brain health and disease. This knowledge could ultimately lead to the development of novel therapeutic strategies that target specific microglial subtypes, with the potential to improve outcomes for individuals with neurological conditions.
We welcome submissions on the following topics, but are not limited to:
- The significant contribution of microglia to brain development and their crucial role in maintaining brain function.
- The diverse functions of microglia including the elimination of excess synapses, generation of new neurons, and the formation of neural networks.
- The dynamic nature of microglia phenotypes and functions, which vary with time and location within the brain.
- The ability of microglia to change their phenotype and function to help control inflammation and promote healing after brain injuries.
- The intricate mechanisms involved in the alteration of genes and cell signals in microglia following brain injuries.
- The pivotal role of microglia in the post-injury cleanup of debris, the maintenance of the blood-brain barrier, and the promotion of neuronal growth.
- The impact of age and sex variations on the response of microglia after a brain injury.
- The potential benefits and complexities of therapeutically targeting microglia due to their multifaceted nature and the possibility of unintended side effects.
Keywords:
microglial, macrophages, phenotypical heterogeneity, functional heterogeneity, neurological disease, neuroinflammation
Important Note:
All contributions to this Research Topic must be within the scope of the section and journal to which they are submitted, as defined in their mission statements. Frontiers reserves the right to guide an out-of-scope manuscript to a more suitable section or journal at any stage of peer review.