Mechanical forces associated with blood flow play important roles in the acute control of vascular tone, the regulation of arterial structure and remodeling, and the localization of atherosclerotic lesions. Major regulation of the blood vessel responses occurs by the action of hemodynamic shear stresses on the endothelium. The transmission of hemodynamic forces throughout the endothelium and the mechanotransduction mechanisms that lead to biophysical, biochemical, and gene regulatory responses of endothelial cells to hemodynamic shear stresses are reviewed.

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Flow-mediated endothelial mechanotransduction

Antithrombotic therapy for venous thromboembolic disease.

Heparin and Low-Molecular-Weight Heparin Mechanisms of Action, Pharmacokinetics, Dosing, Monitoring, Efficacy, and Safety

Membranes are the most common cellular structures in both plants and animals. They are now recognized as being involved in almost all aspects of cellular activity ranging from motility and food entrapment in simple unicellular organisms, to energy transduction, immunorecognition, nerve conduction and biosynthesis in plants and higher organisms. This functional diversity is reflected in the wide variety of lipids and particularly of proteins that compose different membranes. An understanding of the physical principles that govern the molecular organization of membranes is essential for an understanding of their physiological roles since structure and function are much more interdependent in membranes than in, say, simple chemical reactions in solution. We must recognize, however, that the word ‘understanding’ means different things in different disciplines, and nowhere is this more apparent than in this multidisciplinary area where biology, chemistry and physics meet.

/pdf/physical-principles-of-membrane-organization-2enzb9mlqb.pdf

Physical principles of membrane organization.

Platelet-activating factor. Evidence for 1-O-alkyl-2-acetyl-sn-glyceryl-3-phosphorylcholine as the active component (a new class of lipid chemical mediators).

Properties of the factor Xa binding site on human platelets.

http://www.jbc.org/content/249/2/594.full.pdf

The Conversion of Prothrombin to Thrombin I. CHARACTERIZATION OF THE REACTION PRODUCTS FORMED DURING THE ACTIVATION OF BOVINE PROTHROMBIN

Fibrin II monomer has a dramatic inhibitory effect on the rate of heparin-catalyzed inactivation of human alpha-thrombin by antithrombin III. At 6 microM fibrin II monomer, equivalent to the concentration of fibrinogen in plasma, the second-order rate constant was reduced by a factor of 308--from 2.05 x 10(8) M-1.s-1 to 6.65 x 10(5) M-1.s-1. Fibrin II monomer minimally affected the uncatalyzed rate of thrombin inactivation showing a reduction in the second-order rate constant by a factor of only 1.6. Fibrinogen and the product of plasmin degradation of fibrinogen, fragment E, at 6 microM concentrations also decreased the second-order rate constant for heparin-catalyzed thrombin inactivation, but by factors of only 2.7 and 1.9, respectively. On the basis of these observations it is proposed that protection of thrombin from inactivation by heparin-antithrombin III by fibrin II monomer can explain the limited efficacy of heparin in preventing coronary reocclusion in patients treated with tissue plasminogen activator and other fibrinolytic agents.

https://www.pnas.org/content/pnas/86/10/3619.full.pdf

Fibrin monomer protects thrombin from inactivation by heparin-antithrombin III: implications for heparin efficacy

Publisher Summary Amino acid chromogenic and fluorogenic substrates have been used for many years for assaying proteases. The sensitivity of the assay procedures that employ these substrates and the convenience of spectrophotometric or fluorometric measurements has led to their widespread use. Most of the early amino acid chromogenic and fluorogenic substrates are highly selective for the primary specificity-determining (P1) amino acid; thus substrates such as benzoylarginine-p-nitroanilide, for assaying trypsin-like proteases, as well as aromatic amino acidp-nitrophenyl esters for chymotrypsin-like proteases, have been extensively investigated and employed for routine proteolytic enzyme assay. The recognition that both the selectivity of many proteases and their catalytic efficiency depend on interactions with subsite amino acids in the peptide substrate coupled with the availability of amino acid sequences around the cleavage sites in several zymogens of the coagulation and fibrinolytic systems has led to the synthesis and commercial availability of a variety of peptide chromogenic and fluorogenic substrates with much greater selectivity than the single amino acid chromogenic and fluorogenic substrates.

Craig M. Jackson

Papers

Properties of the factor Xa binding site on human platelets.

The Conversion of Prothrombin to Thrombin I. CHARACTERIZATION OF THE REACTION PRODUCTS FORMED DURING THE ACTIVATION OF BOVINE PROTHROMBIN

Fibrin monomer protects thrombin from inactivation by heparin-antithrombin III: implications for heparin efficacy

Assay of coagulation proteases using peptide chromogenic and fluorogenic substrates.

Prothrombin structure, activation, and biosynthesis