دورية أكاديمية

The Prolonged Activation of the p65 Subunit of the NF-Kappa-B Nuclear Factor Sustains the Persistent Effect of Advanced Glycation End Products on Inflammatory Sensitization in Macrophages.

التفاصيل البيبلوغرافية
العنوان: The Prolonged Activation of the p65 Subunit of the NF-Kappa-B Nuclear Factor Sustains the Persistent Effect of Advanced Glycation End Products on Inflammatory Sensitization in Macrophages.
المؤلفون: Assis, Sayonara Ivana Santos de1 (AUTHOR) sayonara.assis@fm.usp.br, Amendola, Leonardo Szalo1 (AUTHOR) leonardo.szalo@usp.br, Okamoto, Maristela Mitiko2 (AUTHOR) mokamoto@icb.usp.br, Ferreira, Guilherme da Silva1 (AUTHOR) ferreira.gui@hotmail.com, Iborra, Rodrigo Tallada3 (AUTHOR) rodrigo.iborra@saojudas.br, Santos, Danielle Ribeiro1 (AUTHOR) danielleribeiro@usp.br, Santana, Monique de Fátima Mello1 (AUTHOR) moniquemelo4@usp.br, Santana, Kelly Gomes1 (AUTHOR) kelly.gomes@hc.fm.usp.br, Correa-Giannella, Maria Lucia4 (AUTHOR) maria.giannella@fm.usp.br, Barbeiro, Denise Frediani5 (AUTHOR) dfbarbeiro@usp.br, Soriano, Francisco Garcia5 (AUTHOR) gsoriano@usp.br, Machado, Ubiratan Fabres2 (AUTHOR) ubiratan@icb.usp.br, Passarelli, Marisa1,6 (AUTHOR) m.passarelli@fm.usp.br
المصدر: International Journal of Molecular Sciences. Mar2024, Vol. 25 Issue 5, p2713. 16p.
مصطلحات موضوعية: *ADVANCED glycation end-products, *RECEPTOR for advanced glycation end products (RAGE), *NF-kappa B, *MACROPHAGES
مستخلص: Advanced glycation end products (AGEs) prime macrophages for lipopolysaccharide (LPS)-induced inflammation. We investigated the persistence of cellular AGE-sensitization to LPS, considering the nuclear content of p50 and p65 nuclear factor kappa B (NFKB) subunits and the expression of inflammatory genes. Macrophages treated with control (C) or AGE-albumin were rested for varying intervals in medium alone before being incubated with LPS. Comparisons were made using one-way ANOVA or Student t-test (n = 6). AGE-albumin primed macrophages for increased responsiveness to LPS, resulting in elevated levels of TNF, IL-6, and IL-1beta (1.5%, 9.4%, and 5.6%, respectively), compared to C-albumin. TNF, IL-6, and IL-1 beta secretion persisted for up to 24 h even after the removal of AGE-albumin (area under the curve greater by 1.6, 16, and 5.2 times, respectively). The expressions of Il6 and RelA were higher 8 h after albumin removal, and Il6 and Abca1 were higher 24 h after albumin removal. The nuclear content of p50 remained similar, but p65 showed a sustained increase (2.9 times) for up to 24 h in AGE-albumin-treated cells. The prolonged activation of the p65 subunit of NFKB contributes to the persistent effect of AGEs on macrophage inflammatory priming, which could be targeted for therapies to prevent complications based on the AGE–RAGE–NFKB axis. [ABSTRACT FROM AUTHOR]
قاعدة البيانات: Academic Search Index
الوصف
تدمد:16616596
DOI:10.3390/ijms25052713