Sex differences of microglia in the healthy brain from embryonic development to adulthood and across lifestyle influences
Open accessAbstract
Microglia, the central nervous system innate immune cells, play a critical role in maintaining a homeostatic environment in the brain throughout life. These cells exhibit an impressive range of functions and characteristics that help to ensure proper functioning of the brain. Notably, microglia can present differences in their genetic and physical traits, which can be influenced by a range of factors, including age, environmental exposures, disease, and sex. Remarkably, microglia have been found to express receptors for sex hormones, suggesting that these hormones may play a role in modulating microglial behavior and potentially contribute to sex differences. Additionally, sex-chromosomal factors were shown to impact microglial genetics and functioning. In this review, we will examine how microglial responses in homeostasis are impacted by their interaction with sex hormones and sex chromosomes. Specifically, our investigation will focus on examining this interaction from embryonic development to adulthood, and the influence of lifestyle elements on various microglial features, including density and distribution, morphology, transcriptome, and proteome.
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Sex determination is led by genes on sex chromosomes and release of sex hormones, especially androgens and estrogens, primarily from gonads, exerting effects on body, brain, and behavior.
“This process is led by genes located on the sex chromosomes and the release of sex hormones, especially androgens and estrogens, coming primarily from the gonads and exerting effects on the body, brain, and behavior [10–13].”
From Sex chromosomes and sex hormones differently shape microglial properties during normal physiological conditions in the adult mouse hippocampus (2025) · cites this paper as [10]
Microglia are highly affected by hormonal and transcriptional changes.
“As microglia are highly affected by hormonal and transcriptional changes, female and male wild-type mice (WT XX and WT XY) were also used for validation [10, 13, 18, 44, 50].”
From Sex chromosomes and sex hormones differently shape microglial properties during normal physiological conditions in the adult mouse hippocampus (2025) · cites this paper as [10]
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References 129 · Cited by 40
- Authors
- Bobotis, B. C., Braniff, O., Gargus, M., Akinluyi, E. T., Awogbindin, I. O., & Tremblay, M.-È.
- Affiliations
- University of Victoria (CA)
- University of Ibadan (NG)
- University of British Columbia (CA)
- Corresponding author
- Tremblay, Marie-Ève
- Venue
- Brain Research Bulletin
- Publisher
- Elsevier BV
- Published
- 2023-10
- Volume
- 202
- Pages
- 110752
- ISSN
- 0361-9230 (ISSN-L)
- OpenAlex
- W4386258420
- Cited by
- 40
- References
- 129
- Citations by year
- 2026: 20 · 2025: 8 · 2024: 10 · 2023: 2
- FWCI
- 1.05
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- Brain Research Bulletin (publishedVersion, cc-by-nc-nd)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- UVic’s Research and Learning Repository (University of Victoria) (submittedVersion)
- UVic’s Research and Learning Repository (University of Victoria) (submittedVersion, cc-by-nc-nd)
- Funders
- Victoria University
- Canadian Institutes of Health Research (461831)
- University of Victoria
- Canada Research Chairs
- Topics
- Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
- Health Sciences › Medicine › Public Health, Environmental and Occupational Health › Sex and Gender in Healthcare
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Keywords
- microglia, sex differences, sex hormones, sex chromosomes, brain homeostasis, embryonic development, microglial morphology, microglial transcriptome, lifestyle factors, innate immunity
- MeSH terms
- Brain, Female, Homeostasis, Humans, Male, Pregnancy, Sex Characteristics, Microglia, Embryonic Development
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