Loss of mir146b with aging contributes to inflammation and mitochondrial dysfunction in thioglycollate-elicited peritoneal macrophages

Andrea C. Santeford, Aaron Y. Lee, Abdoulaye Sene, Lynn M. Hassman, Alexey A. Sergushichev, Ekaterina Loginicheva, Maxim N. Artyomov, Phillip A. Ruzycki, Rajendra S. Apte

Research output: Contribution to journalArticlepeer-review

Abstract

Macrophages undergo programmatic changes with age leading to altered cytokine polarization and immune dysfunction, shifting these critical immune cells from protective sentinels to disease promoters. The molecular mechanisms underlying macrophage inflammaging are poorly understood. Using an unbiased RNA-seq approach, we identified Mir146b as a microRNA whose expression progressively and unidirectionally declined with age in thioglycollate-elicited murine macrophages. Mir146b deficiency led to altered macrophage cytokine expression and reduced mitochondrial metabolic activity, two hallmarks of cellular aging. Single cell RNA sequencing identified patterns of altered inflammation and interferon gamma signaling in Mir146b deficient macrophages. Identification of Mir146b as a potential regulator of macrophage aging provides novel insights into immune dysfunction associated with aging.

Original languageEnglish
Article numbere66703
JournaleLife
Volume10
DOIs
StatePublished - Aug 2021

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