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Dihimo-γ-linolenic acid inhibits several key cellular processes associated with atherosclerosis
- Source :
- Biochimica et Biophysica Acta. Molecular Basis of Disease
- Publication Year :
- 2019
- Publisher :
- Elsevier, 2019.
-
Abstract
- Atherosclerosis and its complications are responsible for one in three global deaths. Nutraceuticals show promise in the prevention and treatment of atherosclerosis but require an indepth understanding of the mechanisms underlying their actions. A previous study showed that the omega-6 fatty acid, dihomo-γ-linolenic acid (DGLA), attenuated atherosclerosis in the apolipoprotein E deficient mouse model system. However, the mechanisms underlying such protective effects of DGLA are poorly understood and were therefore investigated. We show that DGLA attenuates chemokine-driven monocytic migration together with foam cell formation and the expression of key pro-atherogenic genes induced by three pro-inflammatory cytokines in human macrophages. The effect of DGLA on interferon-γ signaling was mediated via inhibition of signal transducer and activator of transcription-1 phosphorylation on serine 727. In relation to anti-foam cell action, DGLA inhibits modified LDL uptake by both macropinocytosis and receptor-mediated endocytosis, the latter by reduction in expression of two key scavenger receptors (SR-A and CD36), and stimulates cholesterol efflux from foam cells. DGLA also improves macrophage mitochondrial bioenergetic profile by decreasing proton leak. Gamma-linolenic acid and prostaglandin E1, upstream precursor and key metabolite respectively of DGLA, also acted in an anti-atherogenic manner. The actions of DGLA extended to other key atherosclerosis-associated cell types with attenuation of endothelial cell proliferation and migration of smooth muscle cells in response to platelet-derived growth factor. This study provides novel insights into the molecular mechanisms underlying the anti-atherogenic actions of DGLA and supports further assessments on its protective effects on plaque regression in vivo and in human trials.<br />Highlights • Dihomo-γ-linolenic acid (DGLA) attenuates atherosclerosis in a mouse model system. • The mechanisms underlying anti-atherogenic actions of DGLA are poorly understood. • DGLA inhibited atherogenic processes in three key cell types in this disease. • Mechanisms underlying such protective actions of DGLA were identified. • Studies inform on the beneficial anti-atherogenic actions of DGLA.
- Subjects :
- Lipopolysaccharides
0301 basic medicine
medicine.medical_treatment
CD36
Interleukin-1beta
NEFA, non esterified fatty acids
Cell
ICAM-1, intercellular adhesion molecule-1
030204 cardiovascular system & hematology
LY, lucifer yellow
TNF-α, tumour necrosis factor-α
VCAM-1, vascular cell adhesion molecule-1
Monocytes
PDGF, platelet-derived growth factor
Mice
chemistry.chemical_compound
8,11,14-Eicosatrienoic Acid
0302 clinical medicine
SR, scavenger receptor
Cell Movement
HASMC, human aortic smooth muscle cells
IFN-γ, interferon-γ
Foam cells
Cells, Cultured
Chemokine CCL2
FCCP, carbonyl cyanide-4-(trifluoromethoxy)phenylhydrazone
Foam cell
Mice, Knockout
HMDM, human monocyte-derived macrophages
AcLDL, acetylated LDL
biology
Chemistry
Intercellular Adhesion Molecule-1
MCP-1, monocyte chemotactic protein-1
Mitochondria
ECM, extracellular matrix
Cell biology
Endothelial stem cell
VSMC, vascular smooth muscle cells
medicine.anatomical_structure
PBMC, peripheral blood mononuclear cells
Smooth muscle cells
Cytokines
LPS, lipopolysaccharide
Molecular Medicine
medicine.symptom
FC, free cholesterol
STAT-1, signal transducer and activator of transcription-1
HUVEC, human umbilical cord endothelial cells
Inflammation
CVD, cardiovascular disease
Article
03 medical and health sciences
TBHP, tert-butyl hydroperoxide
PUFA, polyunsaturated fatty acid
medicine
Animals
Humans
DGLA, dihomo-γ-linolenic acid
oxLDL, oxidized LDL
Scavenger receptor
Molecular Biology
Cell Proliferation
LA, linoleic acid
ABC, ATP-binding cassette transporter
LXR, liver X receptors
Dihomo-γ-linolenic acid
GLA, gamma-linolenic acid
Macrophages
Growth factor
Atherosclerosis
CE, cholesteryl esters
IL, interleukin
030104 developmental biology
Gene Expression Regulation
Apo, apolipoprotein
RT-qPCR, real-time quantitative polymerase chain reaction
biology.protein
Gene expression
PGE1, prostaglandin E1
Subjects
Details
- Language :
- English
- ISSN :
- 09254439
- Database :
- OpenAIRE
- Journal :
- Biochimica et Biophysica Acta. Molecular Basis of Disease
- Accession number :
- edsair.doi.dedup.....2f07a18194f9f9cb47278ac22ed3a1ee