Sadagurski Lab

Neuroinflammation | Metabolism | Environmental Stressors & Aging

Microglia Mediate Metabolic Dysfunction From Common Air Pollutants Through NF-κB Signaling


Journal article


L. Debarba, Hashan Jayarathne, L. Stilgenbauer, Ana L Terra Dos Santos, L. Koshko, S. Scofield, R. Sullivan, A. Mandal, U. Klueh, M. Sadagurski
Diabetes, 2024

Semantic Scholar DOI PubMedCentral PubMed
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APA   Click to copy
Debarba, L., Jayarathne, H., Stilgenbauer, L., Santos, A. L. T. D., Koshko, L., Scofield, S., … Sadagurski, M. (2024). Microglia Mediate Metabolic Dysfunction From Common Air Pollutants Through NF-κB Signaling. Diabetes.


Chicago/Turabian   Click to copy
Debarba, L., Hashan Jayarathne, L. Stilgenbauer, Ana L Terra Dos Santos, L. Koshko, S. Scofield, R. Sullivan, A. Mandal, U. Klueh, and M. Sadagurski. “Microglia Mediate Metabolic Dysfunction From Common Air Pollutants Through NF-ΚB Signaling.” Diabetes (2024).


MLA   Click to copy
Debarba, L., et al. “Microglia Mediate Metabolic Dysfunction From Common Air Pollutants Through NF-ΚB Signaling.” Diabetes, 2024.


BibTeX   Click to copy

@article{l2024a,
  title = {Microglia Mediate Metabolic Dysfunction From Common Air Pollutants Through NF-κB Signaling},
  year = {2024},
  journal = {Diabetes},
  author = {Debarba, L. and Jayarathne, Hashan and Stilgenbauer, L. and Santos, Ana L Terra Dos and Koshko, L. and Scofield, S. and Sullivan, R. and Mandal, A. and Klueh, U. and Sadagurski, M.}
}

Abstract

The prevalence of type 2 diabetes (T2D) poses a significant health challenge, yet the contribution of air pollutants to T2D epidemics remains under-studied. Several studies demonstrated a correlation between exposure to volatile organic compounds (VOCs) in indoor/outdoor environments and T2D. Here, we conducted the first meta-analysis, establishing a robust association between exposure to benzene, a prevalent airborne VOC, and insulin resistance in humans across all ages. We used a controlled benzene exposure system, continuous glucose monitoring approach, and indirect calorimetry in mice, to investigate the underlying mechanisms. Following exposure, disruptions in energy homeostasis, accompanied by modifications in the hypothalamic transcriptome and alterations in insulin and immune signaling, were observed exclusively in males, leading to a surge in blood glucose levels. In agreement, RNA sequencing of microglia revealed increased expression of genes associated with immune response and NF-κB signaling. Selective ablation of IKKβ in immune cells (Cx3cr1GFPΔIKK) or exclusively in microglia (Tmem119ERΔIKK) in adult mice alleviated benzene-induced gliosis, restored energy homeostasis and hypothalamic gene expression, and protected against hyperglycemia. We conclude that the microglial NF-κB pathway plays a critical role in chemical-induced metabolic disturbances, revealing a vital pathophysiological mechanism linking exposure to airborne toxicants and the onset of metabolic diseases. Article Highlights The first meta-analysis, establishing a robust association between exposure to benzene, a prevalent airborne volatile organic compound, and insulin resistance in humans across all ages. Short-term benzene exposure in male mice results in hyperglycemia and disruptions in energy balance. Acute benzene exposure triggers hypothalamic insulin resistance and provokes an inflammatory shift in the microglial transcriptome. The microglial NF-κB pathway is critical in mediating hyperglycemia and metabolic dysregulation induced by benzene exposure.


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