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Experimental study reveals microglial ALKBH5 inhibits fat browning via hypothalamic circuits in male mice, highlighting microglia as potential targets for metabolic disease.
Interactions between nervous system and adipose tissue are involved in the regulation of adipocyte browning. However, whether microglial activation participates in the regulation of cold exposure-induced sympathetic innervation and adipocyte browning is unclear. Here, we demonstrate that RNA m6A demethylase ALKBH5 in the microglia nucleus of hypothalamus (PVH) region inhibits cold exposure-induced adipocyte browning in the subcutaneous white adipose tissue (sWAT) of male mice. The single nuclear-RNA sequencing, brain slice electrophysiological assay and pathological analyses show that microglia-specific ALKBH5 knockout (MCKO) enhances sympathetic activation and adipocyte browning in the sWAT during cold exposure. Mechanistically, MCKO enhances m6A methylation of Ntf5 mRNA and upregulates Ntf5 expression in the microglia. Ntf5 then activates PVH-TrkB neurons and downstream sympathetic innervation in the sWAT. During aging, MCKO prevents brown adipocyte decline in the sWAT, and promotes metabolic activity. These findings fill a gap in the research of microglia in neuron-mediated adipocyte browning, and suggest that microglia may be a potential therapeutic target for the treatment of individuals with metabolic disorders. Interactions between nervous system and adipose tissue are involved in the regulation of adipocyte browning, but the role of microglia is incompletely understood. In this study, the authors demonstrate that RNA m6A demethylase ALKBH5 in the microglia of the nucleus of hypothalamus (PVH) region inhibit cold exposure-induced adipocyte browning in the subcutaneous white adipose tissue of male mice.
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Yang et al. (2026) studied this question.
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