Elevated levels of triglycerides and vldl-cholesterol provoke activation of nlrp1 inflammasome in endothelial cells
Abstract
Background Soluble stimuli present in the plasma of patients with peripheral arterial disease (PAD) are capable of directly stimulating intracellular signalling in endothelium. Oxidized-LDL (oxLDL) induces NLRP3 inflammasome activation in macrophages. However, it is not clear how lipid profile affect NLRP1 inflammasome gene expression in endothelial cells. In this study, the effect of cholesterol and TG of plasma of patients with PAD on NLRP1 inflammasome gene expression in human arterial endothelial cells (HAECS) was assessed. Methods We included 113 patients with symptomatic PAD. HAECs were stimulated for 2h using the plasma samples of the study participants. The NLRP1 quantification of the transcription was carried out on the 7500 real-time PCR system using the Taqman® Universal PCR Master Mix and Assays on demand. Relative quantification of the NLRP1 expression was carried out using the ΔΔCt (threshold cycle) comparative method. Results Plasma from patients with elevated VLDL-cholesterol levels (>33.6mg/dL, the median value of the sample) provoked a higher expression of NLRP1 inflammasome in HAECs (RQ=1.15±0.23 vs. 1.05±0.69; p=0.045), as well as plasma from patients with elevated TGs levels (>168mg/dL, the median value of the sample) (RQ=1.15±0.23 vs. 1.05±0.69; p=0.045). A positive correlation was found between NLRP1 inflammasome expression and VLDL-cholesterol plasma levels (r=0.4; p Conclusions Plasma TG and VLDL cholesterol of patients with atherosclerosis, manifeste…
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Sustained production of these cytokines perpetuates vascular inflammation and influences systemic immune responses, linking metabolic dyslipidemia to chronic inflammatory states that exacerbate atherogenesis.
“Moreover, the sustained production of these cytokines not only perpetuates vascular inflammation but also influences systemic immune responses, linking metabolic dyslipidemia to chronic inflammatory states that exacerbate atherogenesis [19–21].”
From Targeting triglycerides for cardiovascular risk reduction (2026) · cites this paper as [21]
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References 24 · Cited by 47
- Authors
- Bleda, S., de Haro, J., Varela, C., Ferruelo, A., & Acin, F.
- Affiliations
- Hospital Universitario de Getafe (ES)
- Corresponding author
- Bleda, Silvia
- Venue
- International Journal of Cardiology
- Publisher
- Elsevier BV
- Published
- 2016-10
- Volume
- 220
- Pages
- 52-55
- ISSN
- 0167-5273 (ISSN-L)
- OpenAlex
- W2465209004
- Cited by
- 47
- References
- 24
- Citations by year
- 2026: 2 · 2025: 2 · 2024: 3 · 2023: 10 · 2022: 3 · 2021: 6 · 2020: 5 · 2019: 5 · 2018: 4 · 2017: 5 · 2016: 2
- FWCI
- 2.77
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- International Journal of Cardiology (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Inflammasome and immune disorders
- Life Sciences › Immunology and Microbiology › Immunology › Atherosclerosis and Cardiovascular Diseases
- Health Sciences › Medicine › Surgery › Lipoproteins and Cardiovascular Health
- Keywords
- NLRP1 inflammasome, triglycerides, VLDL cholesterol, endothelial cells, peripheral arterial disease, atherosclerosis, plasma lipids, endothelial inflammation
- MeSH terms
- NLR Proteins, Aged, Cells, Cultured, Female, Humans, Male, Middle Aged, Triglycerides, Cholesterol, VLDL, Endothelial Cells, Adaptor Proteins, Signal Transducing, Apoptosis Regulatory Proteins, Peripheral Arterial Disease, Inflammasomes
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