Summary: A new study discovered not all microglia are the same, challenging existing beliefs. A unique subset of these cells, the ARG1+microglia, important for proper cognitive functions, were identified in mice, with evidence suggesting a similar subset exists in humans.
Microglia lacking the protein ARG1 led to less exploratory behavior in mice, indicating cognitive deficits. These discoveries open exciting new possibilities for understanding brain diseases and developing novel therapies.
Not all microglia are the same, with unique subsets like ARG1+microglia having distinct functions in cognitive development and function.
Mice lacking the microglial protein ARG1 displayed less willingness to explore new environments, linking to cognitive deficits and impairments in the hippocampus.
Female animals exhibited more pronounced behavioral and hippocampal impairments caused by ARG1 microglial deficiency, hinting at possible connections to gender biases in diseases like Alzheimer’s.
Source: University of Helsinki
A recent study published in Nature Neuroscience indicates that, contrary to common belief, the immune cells of the brain, known as microglia, are not all the same.
Researchers found that a unique microglial subset with unique features and function is important for establishing proper cognitive functions in mice. Evidence for such microglial subsets exists also for the human brain, opening exciting new possibilities for novel therapies.
An international collaboration led by researchers from University of Helsinki, Karolinska Institutet and University of Seville characterized ARG1+microglia, a subset of microglial cells, that produces the enzyme called arginase-1 (ARG1).
Using advanced imaging techniques, the team found that ARG1+microglia are abundant during development and less prevalent in adult animals. Strikingly, these ARG1+microglia are located in specific brain areas important for cognitive functions such as learning, thinking and memory.
“Cognition and memory are crucial components of what makes us human, and microglia are necessary for proper brain development and function.
“Cognitive decline is a common feature of neurodegenerative and psychiatric conditions like Alzheimer’s and Parkinson’s disease, schizophrenia and depression” says Dr. Vassilis Stratoulias, Senior Researcher at the University of Helsinki and lead author of the study.
“Microglia are involved in virtually all brain pathologies, making them prime candidates for novel drug targets and innovative therapeutic approaches.
“Understanding the fundamental biology of these cells will be the way to produce new directions for drug development to treat currently untreatable diseases of the brain”, adds co-author, Dr. Mikko Airavaara from the University of Helsinki.
Abnormal behavior reveals cognitive deficits
The researchers found that mice lacking the microglial protein ARG1 were less willing to explore new environments. This abnormal rodent behavior is linked to cognitive deficits and, more specifically, to impairments in the hippocampus, a part of the brain important for learning and memory.
The researchers could not identify any differences in the shape of ARG1+microglia when compared to neighboring microglia that do not express ARG1, suggesting a reason why these microglia have not been studied before.
Using a technology that allows for comparison of the RNA profiles between cell populations, ARG1+microglia were found to be significantly different from neighboring ARG1-negative microglia on the molecular level.
Another key finding of the study is that female animals exhibited more pronounced behavioral and hippocampal impairments caused by ARG1 microglial deficiency. Sex bias is present in many diseases including Alzheimer’s disease.
In fact, women are more likely than men to suffer from Alzheimer’s disease – the most common neurodegenerative disease in which cognitive abilities are severely compromised.
Microglia have emerged as key players in Alzheimer’s illness in recent years, making the findings of this study relevant to this disease.
Although more research is needed to demonstrate a link between Alzheimer’s disease and a specific microglial subset, this study could provide a new prism under which we see Alzheimer’s disease in specific – and brain diseases in general – and open new therapeutic pathways.
Dr. Bertrand Joseph, Professor at Karolinska Institutet and senior author says:
“In addition to offering better understanding of brain development and the contribution of microglial diversity to that, the study could provide new clues about how to manage neurodevelopmental disorders or neurodegenerative disorders presenting a cognitive component and often differences between males and females.”
About this neuroscience research news
Author: Aino Pekkarinen Source: University of Helsinki Contact: Aino Pekkarinen – University of Helsinki Image: The top graphic is credited to Neuroscience News. The image in the article is credited to Vassilis Stratoulias
ARG1-expressing microglia show a distinct molecular signature and modulate postnatal development and function of the mouse brain
Molecular diversity of microglia, the resident immune cells in the CNS, is reported. Whether microglial subsets characterized by the expression of specific proteins constitute subtypes with distinct functions has not been fully elucidated.
Here we describe a microglial subtype expressing the enzyme arginase-1 (ARG1; that is, ARG1+ microglia) that is found predominantly in the basal forebrain and ventral striatum during early postnatal mouse development. ARG1+ microglia are enriched in phagocytic inclusions and exhibit a distinct molecular signature, including upregulation of genes such as Apoe, Clec7a, Igf1, Lgals3 and Mgl2, compared to ARG1– microglia.
Microglial-specific knockdown of Arg1 results in deficient cholinergic innervation and impaired dendritic spine maturation in the hippocampus where cholinergic neurons project, which in turn results in impaired long-term potentiation and cognitive behavioral deficiencies in female mice.
Our results expand on microglia diversity and provide insights into microglia subtype-specific functions.