-methyladenosine modification-tuned lipid metabolism controls skin immune homeostasis via regulating neutrophil chemotaxis.

Disrupted -methyladenosine (mA) modification modulates various inflammatory disorders. However, the role of mA in regulating cutaneous inflammation remains elusive. Here, we reveal that the mA and its methyltransferase METTL3 are down-regulated in keratinocytes in inflammatory skin diseases. Inducible deletion of in murine keratinocytes results in spontaneous skin inflammation and increases susceptibility to cutaneous inflammation with activation of neutrophil recruitment. Therapeutically, restoration of mA alleviates the disease phenotypes in mice and suppresses inflammation in human biopsy specimens. We support a model in which mA modification stabilizes the mRNA of the lipid-metabolizing enzyme ELOVL6 via the mA reader IGF2BP3, leading to a rewiring of fatty acid metabolism with a reduction in palmitic acid accumulation and, consequently, suppressing neutrophil chemotaxis in cutaneous inflammation. Our findings highlight a previously unrecognized epithelial-intrinsic mA modification-lipid metabolism pathway that is essential for maintaining epidermal and immune homeostasis and lay the basis for potential therapeutic targeting of mA modulators to attenuate inflammatory skin diseases.