Affiliation:
1. Laboratorio de Neuroinmunobiología, Departamento de Medicina Molecular y Bioprocesos, Instituto de Biotecnología Universidad Nacional Autónoma de México Cuernavaca, Morelos Mexico
Abstract
AbstractBackgroundInflammation in adipose tissue, resulting from imbalanced caloric intake and energy expenditure, contributes to the metabolic dysregulation observed in obesity. The production of inflammatory cytokines, such as IL‐1β and IL‐18, plays a key role in this process. While IL‐1β promotes insulin resistance and diabetes, IL‐18 regulates energy expenditure and food intake. Previous studies have suggested that caspase‐1, activated by the Nlrp3 inflammasome in response to lipid excess, mediates IL‐1β production, whereas activated by the Nlrp1b inflammasome in response to energy excess, mediates IL‐18 production. However, this has not been formally tested.MethodsWild‐type and caspase‐1‐deficient Balb/c mice, carrying the Nlrp1b1 allele, were fed with regular chow or a high‐fat diet for twelve weeks. Food intake and mass gain were recorded weekly. At the end of the twelve weeks, glucose tolerance and insulin resistance were evaluated. Mature IL‐18 protein levels and the inflammatory process in the adipose tissue were determined. Fasting lipid and cytokine levels were quantified in the sera of the different experimental groups.ResultsWe found that IL‐18 production in adipose tissue is independent of caspase‐1 activity, regardless of the metabolic state, while Nlrp3‐mediated IL‐1β production remains caspase‐1 dependent. Additionally, caspase‐1 null Balb/c mice did not develop metabolic abnormalities in response to energy excess from the high‐fat diet.ConclusionOur findings suggest that IL‐18 production in the adipose tissue is independent of Nlrp3 inflammasome and caspase‐1 activation, regardless of caloric food intake. In contrast, Nlrp3‐mediated IL‐1β production is caspase‐1 dependent. These results provide new insights into the mechanisms underlying cytokine production in the adipose tissue during both homeostatic conditions and metabolic stress, highlighting the distinct roles of caspase‐1 and the Nlrp inflammasomes in regulating inflammatory responses.