Sex Differences in the Mitochondrial Bioenergetics of Astrocytes but Not Microglia at a Physiologically Relevant Brain Oxygen Tension
Overview
Authors
Affiliations
Biological sex is thought to influence mitochondrial bioenergetic function. Previous respiration measurements examining brain mitochondrial sex differences were made at atmospheric oxygen using isolated brain mitochondria. Oxygen is 160 mm Hg (21%) in the atmosphere, while the oxygen tension in the brain generally ranges from ∼5 to 45 mm Hg (∼1-6% O). This study tested the hypothesis that sex and/or brain physiological oxygen tension influence the mitochondrial bioenergetic properties of primary rat cortical astrocytes and microglia. Oxygen consumption was measured with a Seahorse XF24 cell respirometer in an oxygen-controlled environmental chamber. Strikingly, male astrocytes had a higher maximal respiration than female astrocytes when cultured and assayed at 3% O. Three percent O yielded a low physiological dissolved O level of ∼1.2% (9.1 mm Hg) at the cell monolayer during culture and 1.2-3.0% O during assays. No differences in bioenergetic parameters were observed between male and female astrocytes at 21% O (dissolved O of ∼19.7%, 150 mm Hg during culture) or between either of these cell populations and female astrocytes at 3% O. In contrast to astrocytes, microglia showed no sex differences in mitochondrial bioenergetic parameters at either oxygen level, regardless of whether they were non-stimulated or activated to a proinflammatory state. There were also no O- or sex-dependent differences in proinflammatory TNF-α or IL-1β cytokine secretion measured at 18 h activation. Overall, results reveal an intriguing sex variance in astrocytic maximal respiration that requires additional investigation. Findings also demonstrate that sex differences can be masked by conducting experiments at non-physiological O.
Sex Differences in Astrocyte Activity.
Gozlan E, Lewit-Cohen Y, Frenkel D Cells. 2024; 13(20.
PMID: 39451242 PMC: 11506538. DOI: 10.3390/cells13201724.
Sex and gender differences in cognitive resilience to aging and Alzheimer's disease.
Arenaza-Urquijo E, Boyle R, Casaletto K, Anstey K, Vila-Castelar C, Colverson A Alzheimers Dement. 2024; 20(8):5695-5719.
PMID: 38967222 PMC: 11350140. DOI: 10.1002/alz.13844.
Bridging metabolic syndrome and cognitive dysfunction: role of astrocytes.
Li Z, Jiang Y, Long C, Peng X, Tao J, Pu Y Front Endocrinol (Lausanne). 2024; 15:1393253.
PMID: 38800473 PMC: 11116704. DOI: 10.3389/fendo.2024.1393253.
Lack of detectable sex differences in the mitochondrial function of Caenorhabditis elegans.
King D, Sparling A, Joyce A, Ryde I, DeSouza B, Ferguson P BMC Ecol Evol. 2024; 24(1):55.
PMID: 38664688 PMC: 11046947. DOI: 10.1186/s12862-024-02238-x.
Fundamental Neurochemistry Review: Microglial immunometabolism in traumatic brain injury.
Strogulski N, Portela L, Polster B, Loane D J Neurochem. 2023; 167(2):129-153.
PMID: 37759406 PMC: 10655864. DOI: 10.1111/jnc.15959.