Abstract
Leptin is associated with cardiometabolic complications of obesity, such as metabolic syndrome and atherosclerosis. In obese men, the presence of metabolic syndrome is associated with higher circulating leptin and interleukin (IL)-6 concentrations and increased monocyte cytokine production capacity. Here, we investigated the effects of leptin on monocyte function and systemic inflammatory markers in obese individuals. We specifically explored whether leptin can induce long-term changes in innate immune function by inducing innate immune memory (also called trained immunity). We exposed human primary monocytes for 24 h to relevant leptin concentrations in vitro and measured cytokine production. In addition, after removing leptin, we incubated monocytes for 5 d in culture medium, and we restimulated them on day 6 to assess cytokine production capacity, phagocytosis, and foam cell formation. Direct stimulation with leptin did not induce cytokine production, but exposure to 50 ng/mL leptin augmented lipopolysaccharide- and R848-induced tumor necrosis factor α (TNF-α) production after 1 wk. In a separate in vivo study in a cohort of 302 obese subjects (body mass index [BMI] >27 kg/m2, 55 to 81 yr), we measured circulating leptin, inflammatory markers, and cytokine production upon ex vivo stimulation of isolated peripheral blood mononuclear cells. Circulating leptin concentrations positively correlated with circulating IL-1β and IL-6, which was more pronounced in men than in women. Four single nucleotide polymorphisms in the leptin gene influenced circulating IL-6 concentrations in men, suggesting a direct effect of leptin on IL-6. In conclusion, in vitro, leptin does not directly stimulate monocytes to produce cytokines, yet induces long-term monocyte hyperresponsiveness, i.e. trained immunity. In obese subjects, leptin is associated with circulating IL-6 in a sex-dependent manner. The underlying mechanisms of the sex-specific effect of leptin on innate immune cells remain to be further investigated.
Original language | English |
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Pages (from-to) | 374–384 |
Number of pages | 11 |
Journal | Journal of Leukocyte Biology |
Volume | 115 |
Issue number | 2 |
Early online date | 30 Sept 2023 |
DOIs | |
Publication status | Published - Feb 2024 |
Externally published | Yes |
Bibliographical note
Publisher Copyright:© 2024 John Wiley and Sons Inc.. All rights reserved.
Funding
J.H.W.R., L.A.B.J., M.G.N., and N.P.R were supported by a CVON grant from the Dutch Heart Foundation and Dutch Cardiovascular Alliance (DCVA; CVON2018-27). N.P.R. was further supported by a grant of the ERA-CVD Joint Transnational Call 2018, which is supported by the Dutch Heart Foundation in the Hague (JTC2018, project MEMORY; 2018T093). S.B. was supported by the Dutch Heart Foundation in the Hague (Dekker grant 2018-T028). M.G.N. was further supported by a European Research Council Advanced Grant (FP/2007-2013/ERC grant 2012-322698) and a Spinoza Prize by NWO (NWO SPI 92-266).
Funders | Funder number |
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Dutch Heart Foundation in the Hague | 2018T093, JTC2018, 2018-T028 |
Dutch Cardiovascular Alliance | CVON2018-27 |
European Research Council | FP/2007-2013/ERC, 2012-322698 |
Hartstichting | |
Nederlandse Organisatie voor Wetenschappelijk Onderzoek | SPI 92-266 |
Keywords
- adipokines
- atherosclerosis
- cytokines
- metabolic syndrome