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A large, functionally and structurally heterogeneous group of transmembrane proteins can undergo cleavage and release of their extracellular domain into the medium.

This proteolytic process is often referred to as “ectodomain shedding” and affects a large set of otherwise unrelated cell surface molecules such as growth factors, growth factor receptors, ectoenzymes, and cell adhesion molecules.

1), a disintegrin-like domain, a Cys-rich moiety, the transmembrane segment, and the intracellular domain.

The trimeric pro-TNFα consists of intracellular segments, transmembrane segments, 26–28 residue spacers forming a stalk, and the compact trimeric TNFα cone (28).

The review begins with established markers of EC injury, commonly soluble markers such as intercellular adhesion molecule-1 (ICAM-1), vascular cell adhesion molecule-1 (VCAM-1), E-selectin, von Willebrand factor (v WF), etc., pointing out that many of these are in fact mixtures of true soluble molecules with membrane-bound forms, i.e., EMP.

Assays of EMP from different labs are reviewed and standardization of assay is recommended.

Certain EMP bind to and activate monocytes; EMP-monocyte conjugates were found to be a marker of inflammatory disease such as multiple sclerosis (MS), and to enhance transendothelial migration of leukocytes in vitro.

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ABSTRACT Endothelial microparticles (EMP) are small vesicles released from disturbed endothelial cells (EC).

Owing to the central importance of EC injury in thrombotic and inflammatory conditions, assay of EMP as a marker of EC disturbance has come under intensive development by several laboratories.

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