Abstract
Cell adhesion under flow is a central function of the microcirculation during inflammation, hemostasis, and immune regulation. This special issue of Microcirculation explores the common and distinct mechanisms that myeloid cells, lymphocytes, platelets, and sickle erythrocytes use to adhere to microvascular endothelium and the underlying basement membrane structures. A common theme in these processes is the need for rapid integrin activation, often initiated by binding of ligands to their cognate G protein–coupled receptors, followed by adhesion strengthening associated with integrin redistribution and outside-in signaling. These elements have been identified for all cells tested except sickle erythrocytes.
Acknowledgements
Declaration of interest: The author reports no financial conflicts of interest. The author alone is responsible for the content and writing of this paper.