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Palmitic but Not Oleic Acid Induces Pro-Inflammatory Dysfunction of Human Endothelial Cells from Different Vascular
Daria Shishkova1, Victoria Markova1, Yulia Yurieva1
1Department of Experimental Medicine, Research Institute for Complex Issues of Cardiovascular Diseases, 6 Barbarash Boulevard, 650002 Kemerovo, Russia.
Palmitic acid (PA) causes significant cell damage and inflammation in human aortic valve and saphenous vein endothelial cells (ECs). Oleic acid (OA) has milder effects, and internal thoracic artery ECs show the most resistance to both fatty acids.
Area of Science:
- Cardiovascular Biology
- Cellular Biology
- Nutritional Science
Background:
- Palmitic acid (PA) and oleic acid (OA) are common dietary fatty acids with distinct properties.
- Endothelial cells (ECs) form the inner lining of blood vessels and play a crucial role in vascular health.
- The differential responses of ECs from various vascular beds to PA and OA are not well understood.
Purpose of the Study:
- To investigate the distinct cytotoxic and pro-inflammatory effects of PA and OA on human ECs from different vascular origins.
- To compare the susceptibility of aortic valve, saphenous vein, internal thoracic artery, and microvascular ECs to these fatty acids.
Main Methods:
- Primary human aortic valve (HAVEC), saphenous vein (HSaVEC), internal thoracic artery (HITAEC), and microvascular (HMVEC) ECs were treated with albumin-bound PA or OA for 24 hours.
- Cytotoxicity was assessed, and gene expression of cell adhesion molecules and pro-inflammatory cytokines was analyzed.
- Release of key inflammatory mediators like interleukin-6 and -8 was measured.
Main Results:
- PA induced significant cytotoxicity and elevated expression of adhesion molecules (VCAM1, ICAM1, SELE, SELP) and pro-inflammatory cytokines in ECs.
- HAVEC and HSaVEC were most susceptible to PA, showing increased interleukin-6 and -8 release.
- OA exhibited mild-to-moderate cytotoxicity in HAVEC and HMVEC without widespread EC activation, while HITAEC demonstrated resistance to both fatty acids.
Conclusions:
- Significant heterogeneity exists in the response of ECs from different vascular beds to palmitic acid.
- Palmitic acid poses a greater risk for endothelial dysfunction compared to oleic acid, particularly in certain vascular ECs.
- Understanding these differential responses is crucial for assessing the vascular impact of dietary fatty acids.
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