A new flow through instrument that simultaneously measures cell volume (resistance pulse technique) and cell fluorescence in the same orifice will be described. The fluorescence pulses of the hydrodynamically focussed cells are picked up by the optics via the axial direction (principle of Dittrich and Goehde, Z Naturforsch 24b:360, 1969).
In a previous clinical study it was found that patients with coronary heart disease and diabetics with peripheral artery disease often have an elevated erythrocyte aggregation value (AW) and that there is a positive correlation between AW and the number of risk factors found in a subject. In the present investigation we studied the relationship between AW and the serum concentration of high density lipoprotein cholesterol (HDL-C), which is known to be inversely associated with coronary heart disease (CHD) incidence. We found highly significant negative correlations between AW and HDL-C both in a subsample of the study population of a cross-sectional epidemiologic study on CHD risk factors (First Survey of the MONICA Project Augsburg) and in male patients with angiographically confirmed CHD. Correlation coefficients were -0.233 for normal men (P less than 0.01, n = 136), -0.261 for normal women (P less than 0.01, n = 117), and -0.745 for CHD patients (P less than 0.01, n = 14). The results support the concept that the erythrocyte aggregation value as an indicator of cardiovascular risk is consistent with established risk factor associations.
The effects of lymphokines on guinea pig peritoneal macrophages were measured via flow cytometry utilizing the three-parameter FLUVO-METRICELL flow cytometer. On the basis of cell volume three distinct macrophage populations could be distinguished. Three to 5 min after starting the incubation with lymphokines a hyperpolarization of all three macrophage populations took place which was followed by depolarization. After 60 min the transmembrane potential reached again its control values. The negative charge density of the cell membrane decreased shortly after beginning of the incubation to 70-80% of the initial value and then remained unchanged for the following 120 min. The phagocytic activity of the macrophages was diminished during the depolarisation phase but increased over control values after restoration of the transmembrane potential.
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