Probing blood cell mechanics of hematologic processes at the single micron level.

Blood cells circulate in a dynamic fluidic environment, and during hematologic processes such as hemostasis, thrombosis, and inflammation, blood cells interact biophysically with a myriad of vascular matrices-blood clots and the subendothelial matrix. While it is known that adherent cells physiologically respond to the mechanical properties of their underlying matrices, how blood cells interact with their mechanical microenvironment of vascular matrices remains poorly understood. To that end, we developed microfluidic systems that achieve high fidelity, high resolution, single-micron PDMS features that mimic the physical geometries of vascular matrices. With these electron beam lithography (EBL)-based microsystems, the physical interactions of individual blood cells with the mechanical properties of the matrices can be directly visualized. We observe that the physical presence of the matrix, in and of itself, mediates hematologic processes of the three major blood cell types: platelets, erythrocytes, and leukocytes. First, we find that the physical presence of single micron micropillars creates a shear microgradient that is sufficient to cause rapid, localized platelet adhesion and aggregation that leads to complete microchannel occlusion; this response is enhanced with the presence of fibrinogen or collagen on the micropillar surface. Second, we begin to describe the heretofore unknown biophysical parameters for the formation of schistocytes, pathologic erythrocyte fragments associated with various thrombotic microangiopathies (poorly understood, yet life-threatening blood disorders associated with microvascular thrombosis). Finally, we observe that the physical interactions with a vascular matrix is sufficient to cause neutrophils to form procoagulant neutrophil extracellular trap (NET)-like structures. By combining electron beam lithography (EBL), photolithography, and soft lithography, we thus create microfluidic devices that provide novel insight into the response of blood cells to the mechanical microenvironment of vascular matrices and have promise as research-enabling and diagnostic platforms.

Effects of dietary inclusion of cornelian cherry (Cornus mas L.) fruit on body weight, insulin level and glycemic status of hamsters.

The aim of present experiment was to investigate the effect of dietary supplemented CCF on body weight, serum glucose and insulin in healthy condition. In present experiment, 36 one-month-old male hamsters (94 +/- 1 g) were divided into four groups; group 1 (control): fed basal diets without fruit supplementation, group 2: fed daily 5 g CCF only at first daily meal, group 3: fed daily 10 g CCF, at first and second daily meals and group 4: fed daily 15 g CCF, at first, second and third daily meals, for 20 days. Dietary CCF caused significant decreases in final body weight. Based on serum biochemical analysis, a significant glucose decrease in groups fed only one supplemented meal and it's correlated with elevation of insulin level. Supplementation of CCF (two or three times daily) was not efficient for more hypoglycemic effect and there was no significant difference with glucose level of control group. Also, there was no any difference between insulin levels of group 2 and 3, whereas there was considerable elevation in insulin level for groups fed CCF in comparison with control rate. It was concluded that supplemented cornelian cherry fruit for one, two or three daily meal can decreases weight gain and for only one daily meal can cause considerable hypoglycemic effect, whereas supplemented for two or three times daily was not more efficient that may be due to glycemic regulation of healthy animals.