ReferenceID 2019

Alantolactone Enhances the Phagocytic Properties of Human Macrophages and Modulates Their Proinflammatory Functions

Front Pharmacol

Aim of the Study: Phagocytosis is a crucial element of innate immune defense involved in bacterial killing. The aim of our study was to evaluate the influence of alantolactone on phagocytosis and cytokines release by THP

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Reference Id
2019
Evidence Id
18609
Core Evidence Id
18609
Source Reference Id
4049
Herb2 Reference Id
HBREF004846
Subject Paper Key
HBIN028928_33013371
Pubmed Id
33013371
Doi
10.3389/fphar.2020.01339
Paper Title
Alantolactone Enhances the Phagocytic Properties of Human Macrophages and Modulates Their Proinflammatory Functions
Paper Abstract
Aim of the Study: Phagocytosis is a crucial element of innate immune defense involved in bacterial killing. The aim of our study was to evaluate the influence of alantolactone on phagocytosis and cytokines release by THP1-derived macrophages. We assessed whether antimicrobial compound alantolactone (a sesquiterpene lactone present in Inula helenium L.) is able to stimulate immune functions of macrophages by increase of S. aureus uptake, phagosome acidification and further stimulation of phago-lysosomes formation. Simultaneously, we tested influence of alantolactone on cytokines/chemokines production and p65 NF-kappaB concentration. The activity of alantolactone was compared with clarithromycin at concentration 20 microM. Methods: The cytotoxicity of alantolactone as well as S. aureus uptake, pH of phagosomes and phago-lysosomes fusion were analysed with flow cytometry. Reactive oxygen species and superoxide production were evaluated spectrophotometrically. The efficiency of phagocytosis was evaluated via quantifying viable bacteria (CFU). The effect on p65 protein concentration and cytokine production by macrophages were measured by enzyme-linked immunosorbent assay (ELISA). Results: Alantolactone enhanced phagocytosis via increase of S. aureus uptake, acidification of phagosomes, and later stimulation of phago-lysosomes fusion. Alantolactone treatment resulted in ROS and superoxide production decrease. Furthermore, alantolactone inhibited production of pro-inflammatory cytokines TNF-alpha, IL-1beta, IL-6, and IL-8 as well as decreased p65 concentration, the subunit responsible for NF-kappaB activation and cytokine production and simultaneously stimulated release of anti-inflammatory mediators (IL-10 and TGF-beta). Conclusion: Results of our study indicate that alantolactone enhances clearance of S. aureus, and simultaneously modulates immune response, preventing collateral damage of the surrounding tissues. Considering the importance of phagocytosis in the pathogen killing, alantolactone may have a great potential as the supportive treatment of S. aureus infections. Further in vivo studies are warranted to confirm this hypothesis.
Journal
Front Pharmacol
Publish Year
2020
Experiment Subject
Experiment Type
Cell Experiment
Phenotype Related
S. Aureus Infections
Paper Title Cn
Paper Title En
Alantolactone Enhances the Phagocytic Properties of Human Macrophages and Modulates Their Proinflammatory Functions
Bilingual Status
semi_complete