Inclisiran inhibits oxidized low-density lipoprotein-induced foam cell formation in Raw264.7 macrophages via activating the PPARγ pathway
Abstract
Proprotein convertase subtilisin kexin type 9 (PCSK9) is a well-known proprotein convertase that influences foam cell formation and modulates atherosclerosis. Inclisiran is a novel chemosynthetic small interfering RNA that inhibits PCSK9 synthesis. This study aimed to explore the effect of inclisiran on oxidized low-density lipoprotein (ox-LDL)-induced foam cell formation in Raw264.7 macrophages and to investigate the underlying mechanisms. Raw264.7 cells were treated with ox-LDL to induce the formation of macrophage-derived foam cells. Oil Red O staining and high-performance liquid chromatography were performed to detect lipid accumulation and cholesterol levels. Dil-ox-LDL uptake assay, CCK-8, RT-qPCR, and Western blotting analysis were performed to examine ox-LDL uptake, cell viability, and expression of scavenger receptor-related factors. Inclisiran reduced lipid accumulation in ox-LDL-treated macrophages in a dose-dependent manner. Inclisiran significantly inhibited the levels of total cholesterol, free cholesterol, and cholesterol ester in the supernatant of Raw264.7 cells. Inclisiran reduced ox-LDL uptake and increased Raw264.7 cell viability. Meanwhile, inclisiran downregulated the expression of SR-A, LOX-1, and CD36 and upregulated SR-BI, ApoE, and ABCA1. Furthermore, inclisiran increased PPARγ activity and decreased NF-κB activity. An inhibitor of PPARγ (T0070907) reversed the beneficial effects of inclisiran on ox-LDL uptake, NF-κB inactivation, and cytokine expres…
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Through intracellular PCSK9 reduction, inclisiran enhances liver cell LDL receptor recycling, which results in higher receptor density and improved removal of blood LDL particles.
“Through intracellular PCSK9 reduction Inclisiran enhances liver cell LDL receptor recycling which results in higher receptor density and improved removal of blood LDL particles [9, 67].”
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References 47 · Cited by 16
- Authors
- Wang, Z., Chen, X., Liu, J., Wang, Y., & Zhang, S.
- Affiliations
- Shandong University (CN)
- Weihai Municipal Hospital (CN)
- Emergency Department, Qingdao Municipal Hospital (Group), Qingdao NO.9 People’s Hospital, Qingdao, P.R. China
- Corresponding author
- Wang, Yingcui
- Zhang, Suhua
- Venue
- Autoimmunity
- Publisher
- Informa UK Limited
- Published
- 2022-03-15
- Volume
- 55
- Issue
- 4
- Pages
- 223-232
- ISSN
- 0891-6934 (ISSN-L)
- 1607-842X
- OpenAlex
- W4221046064
- Cited by
- 16
- References
- 47
- Citations by year
- 2026: 3 · 2025: 3 · 2024: 4 · 2023: 3 · 2022: 3
- FWCI
- 3.11
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Autoimmunity (publishedVersion)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion)
- Topics
- Health Sciences › Medicine › Surgery › Cholesterol and Lipid Metabolism
- Life Sciences › Immunology and Microbiology › Immunology › Atherosclerosis and Cardiovascular Diseases
- Health Sciences › Medicine › Surgery › Lipoproteins and Cardiovascular Health
- Keywords
- inclisiran, PCSK9 inhibition, oxidized LDL, foam cell formation, macrophages, PPARγ, NF-κB, scavenger receptors, cholesterol accumulation, atherosclerosis, siRNA
- MeSH terms
- Proprotein Convertase 9, Cholesterol, Foam Cells, Humans, Lipoproteins, LDL, Macrophages, NF-kappa B, RNA, Small Interfering, PPAR gamma, Atherosclerosis
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