Sex differences in somatosensory circuitry are programmed by developmental microglia-astrocyte interaction

Men possess a greater density of cortical synapses in the adult brain relative to women, but the underlying mechanism and functional significance of this sex difference is unclear. Here, we identify a greater density of excitatory synapses in the male mouse somatosensory cortex (S1) which emerges during development and persists into the adult brain. We show that increased phagocytic activity in microglia of female mice causes a greater engulfment of astrocytes in the female S1 in a MERTK-dependent manner during a discrete developmental window, regulated at least in part by estrogen signaling. The resulting greater astrocyte density in males corresponds with an increase in astrocyte-derived synaptogenic factors, hevin and thrombospondin-2, which we propose leads to the observed sex difference in S1 synapse density. Moreover, we demonstrate that this sex difference in synapse density correlates with an increase in neuronal activity in the male S1 both in development and adulthood.

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Publication Details

Journal
Cell Reports
Published
2026-07-25
DOI
https://doi.org/10.1016/j.celrep.2026.117709
Primary Topic
Neuroinflammation and Neurodegeneration Mechanisms
Type
article
Field-Weighted Citation Impact
0.00

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article

Sex differences in somatosensory circuitry are programmed by developmental microglia-astrocyte interaction

Ukpong B. Eyo, Madison Doceti, J. M. Thomas, Leigh Ellen Fremuth et al.
Cell Reports
Neuroinflammation and Neurodegeneration Mechanisms
article

Sex differences in somatosensory circuitry are programmed by developmental microglia-astrocyte interaction

Ukpong B. Eyo, Madison Doceti, J. M. Thomas, Leigh Ellen Fremuth, Osaretin Lawani, Abigayle Duffy, Charlotte Buswell, John R. Lukens
article en

Abstract

Men possess a greater density of cortical synapses in the adult brain relative to women, but the underlying mechanism and functional significance of this sex difference is unclear. Here, we identify a greater density of excitatory synapses in the male mouse somatosensory cortex (S1) which emerges during development and persists into the adult brain. We show that increased phagocytic activity in microglia of female mice causes a greater engulfment of astrocytes in the female S1 in a MERTK-dependent manner during a discrete developmental window, regulated at least in part by estrogen signaling. The resulting greater astrocyte density in males corresponds with an increase in astrocyte-derived synaptogenic factors, hevin and thrombospondin-2, which we propose leads to the observed sex difference in S1 synapse density. Moreover, we demonstrate that this sex difference in synapse density correlates with an increase in neuronal activity in the male S1 both in development and adulthood.

Cell ReportsVol. 45(8)
University of Virginia (US)
Owens Family Foundation, National Institutes of Health
Gender equality
Openalex Percentile: Top 10%
Neuroinflammation and Neurodegeneration Mechanisms
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