A shift in PKM2 oligomeric state instructs adipocyte inflammatory potential

Processes that promote white adipocyte inflammatory function remain incompletely defined. Here, we demonstrated that type I interferon-dependent (IFN-I-dependent) skewing of adipocyte glycolysis, nicotinamide adenine dinucleotide (NAD+) utilization, and pyruvate kinase isozyme M2 (PKM2) function may contribute to increased systemic and tissue inflammation and disease severity in obesity. Notably, chemical and/or genetic inhibition of glycolysis, the NAD+ salvage pathway, or PKM2 restricted IFN-I-dependent increase in adipocyte inflammatory cytokine production. Further, genetic or small molecule targeting of PKM2 function in vivo was sufficient to reduce systemic and tissue inflammation and metabolic disease severity in obese mice, in an adipocyte PKM2-dependent manner. Further, white adipose tissue of individuals living with obesity and metabolic disease, compared with metabolically healthy individuals with obesity, showed an increase in expression of inflammatory and metabolic genes, while small molecule targeting of PKM2 function contributed to reduced IFN-I-driven inflammatory cytokine production by primary human adipocytes. Together, our findings invoke the IFN-I/PKM2 axis as a potential target for modulating adipocyte dysregulated inflammation.

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Publication Details

Journal
JCI Insight
Published
2025-11-23
DOI
https://doi.org/10.1172/jci.insight.185914
Citations
1
Primary Topic
Adipokines, Inflammation, and Metabolic Diseases
Type
article
Field-Weighted Citation Impact
1.35
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article

A shift in PKM2 oligomeric state instructs adipocyte inflammatory potential

Jennifer L. Wayland, Traci E. Stankiewicz, Sara Szabo, Keisuke Sawada et al.
1 citations
JCI Insight
Adipokines, Inflammation, and Metabolic Diseases
1.35
article

A shift in PKM2 oligomeric state instructs adipocyte inflammatory potential

Jennifer L. Wayland, Traci E. Stankiewicz, Sara Szabo, Keisuke Sawada, Senad Divanovic, Miki Watanabe‐Chailland, Pablo C. Alarcon, Jessica Doll, Lindsey E. Romick‐Rosendale, Joan Sánchez-Gurmaches, Michael A. Helmrath, Maria E. Moreno‐Fernandez, Michelle S. M. A. Damen, Jung Seop Eom, Jarren R. Oates, Rajib Mukherjee, Hak‐Jae Chung, Calvin C. Chan, Cassidy J Ulanowicz
article en
1 citations

Abstract

Processes that promote white adipocyte inflammatory function remain incompletely defined. Here, we demonstrated that type I interferon-dependent (IFN-I-dependent) skewing of adipocyte glycolysis, nicotinamide adenine dinucleotide (NAD+) utilization, and pyruvate kinase isozyme M2 (PKM2) function may contribute to increased systemic and tissue inflammation and disease severity in obesity. Notably, chemical and/or genetic inhibition of glycolysis, the NAD+ salvage pathway, or PKM2 restricted IFN-I-dependent increase in adipocyte inflammatory cytokine production. Further, genetic or small molecule targeting of PKM2 function in vivo was sufficient to reduce systemic and tissue inflammation and metabolic disease severity in obese mice, in an adipocyte PKM2-dependent manner. Further, white adipose tissue of individuals living with obesity and metabolic disease, compared with metabolically healthy individuals with obesity, showed an increase in expression of inflammatory and metabolic genes, while small molecule targeting of PKM2 function contributed to reduced IFN-I-driven inflammatory cytokine production by primary human adipocytes. Together, our findings invoke the IFN-I/PKM2 axis as a potential target for modulating adipocyte dysregulated inflammation.

JCI InsightVol. 10(22)
Cincinnati Children's Hospital Medical Center (US), University of Cincinnati Medical Center (US)
Openalex Percentile: Top 14%
Adipokines, Inflammation, and Metabolic Diseases
1.35
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