Castelo Janire, Araujo-Aris Sarai, Barriales Diego, Tanner Pasco Samuel, Seoane Iratxe, Peña-Cearra Ainize, Palacios Ainhoa, Simó Carolina, Garcia-Cañas Virginia, Khamwong Muthita, Martín-Ruiz Itziar, Gonzalez-Lopez Monika, Barcena Laura, Martín Rodríguez José Ezequiel, Lavín José Luís, Gutiez Naiara, Marcos Raquel, Atondo Estibaliz, Cobela Arantza, Plaza-Vinuesa Laura, Plata Adrián, Santos-Fernandez Eneko, Fernandez-Tejada Alberto, Villarán Mari Carmen, Mancheño José Miguel, Maria Flores Juana, María Aransay Ana, Pellón Aize, de Las Rivas Blanca, Muñoz Rosario, Margolles Abelardo, Ruas-Madiedo Patricia, Victoria Selma Maria, Gomez de Agüero Mercedes, Abecia Leticia, Anguita Juan, Rodríguez Héctor
CIC bioGUNE, Basque Research and Technology Alliance (BRTA), Derio, Spain.
Department of Immunology, Microbiology and Parasitology, Faculty of Medicine and Nursing, University of the Basque Country (UPV/EHU), Bilbao, Spain.
Gut Microbes. 2024 Jan-Dec;16(1):2438829. doi: 10.1080/19490976.2024.2438829. Epub 2024 Dec 15.
Phloroglucinol is a key byproduct of gut microbial metabolism that has been widely used as a treatment for irritable bowel syndrome. Here, we demonstrate that phloroglucinol tempers macrophage responses to pro-inflammatory pathogens and stimuli. , phloroglucinol administration decreases gut and extraintestinal inflammation in murine models of inflammatory bowel disease and systemic infection. The metabolite induces modest modifications in the microbiota. However, the presence of an active microbiota is required to preserve its anti-inflammatory activity. Remarkably, the protective effect of phloroglucinol lasts partially at least 6 months. Single-cell transcriptomic analysis of bone marrow progenitors demonstrates the capacity of the metabolite to induce long-lasting innate immune training in hematopoietic lineages, at least partially through the participation of the receptor and transcription factor, aryl hydrocarbon receptor (AhR). Phloroglucinol induces alterations in metabolic and epigenetic pathways that are most prevalent in upstream progenitors as hallmarks of central trained immunity. These data identify phloroglucinol as a dietary-derived compound capable of inducing central trained immunity and modulating the response of the host to inflammatory insults.
间苯三酚是肠道微生物代谢的一种关键副产物,已被广泛用作治疗肠易激综合征的药物。在此,我们证明间苯三酚可调节巨噬细胞对促炎性病原体和刺激的反应。此外,在炎性肠病和全身感染的小鼠模型中,给予间苯三酚可减轻肠道和肠外炎症。该代谢产物会引起微生物群的适度改变。然而,需要有活性的微生物群来维持其抗炎活性。值得注意的是,间苯三酚的保护作用至少部分持续6个月。对骨髓祖细胞进行单细胞转录组分析表明,该代谢产物能够在造血谱系中诱导持久的先天性免疫训练,至少部分是通过芳烃受体(AhR)这一受体和转录因子的参与实现的。间苯三酚会诱导代谢和表观遗传途径发生改变,这些改变在上游祖细胞中最为普遍,是中枢训练性免疫的标志。这些数据表明间苯三酚是一种源自饮食的化合物,能够诱导中枢训练性免疫并调节宿主对炎症刺激的反应。