Document Type
Article
Publication Date
2-3-2021
Abstract
In obesity, adipose tissue derived inflammation is associated with unfavorable metabolic consequences. Uremic inflammation is prevalent and contributes to detrimental outcomes. However, the contribution of adipose tissue inflammation in uremia has not been characterized. We studied the contribution of adipose tissue to uremic inflammation in-vitro, in-vivo and in human samples. Exposure to uremic serum resulted in activation of inflammatory pathways including NFκB and HIF1, upregulation of inflammatory cytokines/chemokines and catabolism with lipolysis, and lactate production. Also, co-culture of adipocytes with macrophages primed by uremic serum resulted in higher inflammatory cytokine expression than adipocytes exposed only to uremic serum. Adipose tissue of end stage renal disease subjects revealed increased macrophage infiltration compared to controls after BMI stratification. Similarly, mice with kidney disease recapitulated the inflammatory state observed in uremic patients and additionally demonstrated increased peripheral monocytes and inflammatory polarization of adipose tissue macrophages (ATMS). In contrast, adipose tissue in uremic IL-6 knock out mice showed reduced ATMS density compared to uremic wild-type controls. Differences in ATMS density highlight the necessary role of IL-6 in macrophage infiltration in uremia. Uremia promotes changes in adipocytes and macrophages enhancing production of inflammatory cytokines. We demonstrate an interaction between uremic activated macrophages and adipose tissue that augments inflammation in uremia.
Recommended Citation
Martos-Rus, Cristina; Katz-Greenberg, Goni; Lin, Zhao; Serrano, Eurico; Menezes, Diana Whitaker; Domingo-Vidal, Marina; Roche, Megan; Ramaswamy, Kavitha; Hooper, D. Craig; Falkner, Bonita; and Martinez Cantarin, Maria P, "Macrophage and adipocyte interaction as a source of inflammation in kidney disease" (2021). Kimmel Cancer Center Faculty Papers. Paper 75.
https://jdc.jefferson.edu/kimmelccfp/75
Creative Commons License
This work is licensed under a Creative Commons Attribution 4.0 License.
PubMed ID
33536542
Language
English
Comments
This article is the author’s final published version in Scientific Reports, Volume 11, Issue 1, December 2021, Article number 2974.
The published version is available at https://doi.org/10.1038/s41598-021-82685-4. Copyright © Martos-Rus et al.