Mechanosensing at the vascular interface

JM Tarbell, SI Simon, FRE Curry - Annual review of biomedical …, 2014 - annualreviews.org
JM Tarbell, SI Simon, FRE Curry
Annual review of biomedical engineering, 2014annualreviews.org
Mammals are endowed with a complex set of mechanisms that sense mechanical forces
imparted by blood flow to endothelial cells (ECs), smooth muscle cells, and circulating blood
cells to elicit biochemical responses through a process referred to as mechanotransduction.
These biochemical responses are critical for a host of other responses, including regulation
of blood pressure, control of vascular permeability for maintaining adequate perfusion of
tissues, and control of leukocyte recruitment during immunosurveillance and inflammation …
Mammals are endowed with a complex set of mechanisms that sense mechanical forces imparted by blood flow to endothelial cells (ECs), smooth muscle cells, and circulating blood cells to elicit biochemical responses through a process referred to as mechanotransduction. These biochemical responses are critical for a host of other responses, including regulation of blood pressure, control of vascular permeability for maintaining adequate perfusion of tissues, and control of leukocyte recruitment during immunosurveillance and inflammation. This review focuses on the role of the endothelial surface proteoglycan/glycoprotein layer—the glycocalyx (GCX)—that lines all blood vessel walls and is an agent in mechanotransduction and the modulation of blood cell interactions with the EC surface. We first discuss the biochemical composition and ultrastructure of the GCX, highlighting recent developments that reveal gaps in our understanding of the relationship between composition and spatial organization. We then consider the roles of the GCX in mechanotransduction and in vascular permeability control and review the prominent interaction of plasma-borne sphingosine-1 phosphate (S1P), which has been shown to regulate both the composition of the GCX and the endothelial junctions. Finally, we consider the association of GCX degradation with inflammation and vascular disease and end with a final section on future research directions.
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