The Role of Senescence-Associated Interferon in Age-Related Inflammation

TL;DR

This study shows that senescent monocytes contribute to age-related inflammation through interferon signaling, and targeting these cells could reduce harmful immune responses in older individuals.

Contribution

The study identifies senescence-associated interferon signaling as a novel driver of inflammaging and potential therapeutic target.

Findings

Senescent monocytes show increased interferon-related proteins and reduced inflammatory responses with targeted interventions.

Proteomic analysis of circulating monocytes identified 27 senescence-associated proteins linked to systemic inflammation markers like CRP.

Senescent monocytes exhibit a heightened cytokine response to LPS, contributing to inflammaging and immune hyperactivation.

Abstract

Inflammaging, age-related deterioration of immune function, features persistent inflammation alongside an exacerbated immune response to pathogens. Senescent monocytes accumulate with age and release harmful proteins, potentially driving hyperinflammation. This study explores how senescent monocytes contribute to inflammaging and evaluates therapeutic interventions targeting these cells. Using an irradiation-induced senescence model in THP-1 monocytes, we analyzed the proteomic changes via data-independent acquisition (DIA) mass spectrometry. We assessed the impact of senescence on pathogen response by measuring LPS-induced inflammatory cytokines in senescent and non-senescent cells using a Mesoscale kit. Additionally, we tested various compounds for their ability to modulate inflammation and evaluated inflammatory signatures in monocytes. Finally, we examined proteomic profiles of circulating monocytes from 94 individuals aged 22-89 in the Genetic and Epigenetic Signatures of Translational Aging Laboratory Testing (GESTALT) study of aging to identify clinical associations between senescence and IFN signatures and aging phenotypes in vivo. Senescent THP-1 monocytes exhibited significant proteome remodeling, with increased 359 IFN-related proteins, including STAT1, OAS1, OAS2, MX1, and ISG15, while 1355 decreased proteins. Moreover, when stimulated with LPS, senescent monocytes exhibited a highly potentiated inflammatory cytokine response, including interleukins and IFN-ƴ, driving inflammaging and susceptibility. Notably, interventions targeting senescence or IFN signaling reduced these inflammatory responses. Further, the proteomic analysis of circulating monocytes in the GESTALT cohort showed that 27 senescence-associated proteins, correlated with CRP, were identified as potential biomarkers, highlighting systemic inflammation. These findings highlight senescence-associated IFN signaling as a key driver of inflammaging and suggest potential therapeutic strategies to mitigate age-related immune dysregulation.