Abstract

Major factors leading to the development of atherosclerosis are a high cholesterol (Chol) level in the blood and oxidative stress. Both promote the formation of Chol microcrystals in blood vessel walls. Deposition of Chol microcrystals in arterial intima causes inflammation, which initiates and accompanies the atherosclerotic process in all its phases. One of the possible sources of Chol in the blood vessel walls is oxidized low-density lipoproteins—this atherosclerotic plaque formation pathway has already been described in the literature. Here, we hypothesize that initiation of the atherosclerotic process may involve Chol domains in the plasma membranes of arterial cells. Increased Chol content and the presence of polyunsaturated phospholipids in these membranes together with oxidative stress (phospholipid peroxidation) may lead to the formation of pure Chol bilayer domains that, with further peroxidation and increased Chol content, may collapse in the form of Chol seed crystals. Independent of their origin, Chol microcrystals activate inflammasomes, thereby stimulate immune responses, and initiate inflammation that may lead to the development of atherosclerosis. This new, hypothetical pathway has not yet been investigated in depth; however, data from the literature and our own results support its feasibility.

Highlights

  • Biological and clinical research indicates a fundamental and initiating role of inflammation in atherosclerosis [1, 2]

  • In experiments on germ-free mice fed on a highcholesterol diet leading to atherosclerosis development, Duewell et al [8] showed that detection of Chol microcrystals in early atherosclerotic lesions coincided with the appearance of inflammatory cells

  • The formation of Chol bilayer domains (CBD) precedes the formation of Chol crystals

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Summary

Introduction

Biological and clinical research indicates a fundamental and initiating role of inflammation in atherosclerosis [1, 2]. Independent of the pathway of Chol microcrystals formation in vascular wall, the crystals can activate inflammasomes and induce inflammation, which may lead to the development of atherosclerosis. When the Chol content in the phospholipid bilayer further increases and exceeds the Chol solubility threshold [17, 18, 20, 30, 31], Chol crystals form, presumably outside the membrane [31,32,33].

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