Microbial Interactions Laboratory, Faculty of Dentistry, Universidad Andrés Bello, Santiago 8370133, Chile.
Advanced Center for Chronic Diseases (ACCDiS), Faculty of Medicine, Universidad de Chile, Santiago 8380453, Chile.
Int J Mol Sci. 2024 Mar 23;25(7):3611. doi: 10.3390/ijms25073611.
Periodontitis, characterized by persistent inflammation in the periodontium, is intricately connected to systemic diseases, including oral cancer. Bacteria, such as and , play a pivotal role in periodontitis development because they contribute to dysbiosis and tissue destruction. Thus, comprehending the interplay between these bacteria and their impacts on inflammation holds significant relevance in clinical understanding and treatment advancement. In the present work, we explored, for the first time, their impacts on the expressions of pro-inflammatory mediators after infecting oral keratinocytes (OKs) with a co-culture of pre-incubated and . Our results show that the co-culture increases IL-1β, IL-8, and TNF-α expressions, synergistically augments IL-6, and translocates NF-kB to the cell nucleus. These changes in pro-inflammatory mediators-associated with chronic inflammation and cancer-correlate with an increase in cell migration following infection with the co-cultured bacteria or alone. This effect depends on TLR4 because TLR4 knockdown notably impacts IL-6 expression and cell migration. Our study unveils, for the first time, crucial insights into the outcomes of their co-culture on virulence, unraveling the role of bacterial interactions in polymicrobial diseases and potential links to oral cancer.
牙周炎的特征是牙周组织持续炎症,与包括口腔癌在内的系统性疾病有着错综复杂的联系。细菌,如 和 ,在牙周炎的发展中起着关键作用,因为它们导致了菌群失调和组织破坏。因此,理解这些细菌之间的相互作用及其对炎症的影响,在临床理解和治疗进展方面具有重要意义。在本工作中,我们首次探索了它们在将预先孵育的 和 共培养物感染口腔角质细胞(OK)后对促炎介质表达的影响。我们的结果表明,共培养物协同增加了 IL-6 的表达,并增加了 IL-1β、IL-8 和 TNF-α 的表达,同时将 NF-kB 易位到细胞核。这些与慢性炎症和癌症相关的促炎介质的变化,与感染共培养细菌或 单独感染后细胞迁移的增加相关。这种效应依赖于 TLR4,因为 TLR4 的敲低显著影响了 IL-6 的表达和细胞迁移。我们的研究首次揭示了它们共培养对毒力的重要结果,揭示了细菌相互作用在多微生物疾病中的作用以及与口腔癌的潜在联系。