Article ID Journal Published Year Pages File Type
6087446 Clinical Immunology 2014 13 Pages PDF
Abstract

•Membrane lipids are altered during intestinal ischemia/reperfusion.•Eicosanoids are required but not sufficient for intestinal ischemia/reperfusion-induced injury.•Membrane lipid alterations result in neoantigen exposure to initiate injury in response to intestinal ischemia/reperfusion•Phospholipid scramblase 1 appears to induce intestinal lipid alterations during ischemia/reperfusion.

Ischemia, lack of blood flow, and reperfusion, return of blood flow, are a common phenomenon affecting millions of Americans each year. Roughly 30,000 Americans per year experience intestinal ischemia-reperfusion (IR), which is associated with a high mortality rate. Previous studies of the intestine established a role for neutrophils, eicosanoids, the complement system and naturally occurring antibodies in IR-induced pathology. Furthermore, data indicate involvement of a lipid or lipid-like moiety in mediating IR-induced damage. It has been proposed that antibodies recognize exposure of neo-antigens, triggering action of the complement cascade. While it is evident that the pathophysiology of IR-induced injury is complex and multi-factorial, we focus this review on the involvement of eicosanoids, phospholipids and neo-antigens in the early pathogenesis. Lipid changes occurring in response to IR, neo-antigens exposed and the role of a phospholipid transporter, phospholipid scramblase 1 will be discussed.

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