Light paths in retinal vessel oxymetry.

The oxygen utilization and, therefore, the metabolic state, of a distinctive area of the retina may be calculated from the diameter of the supplying artery and vein, the haemoglobin oxygenation, and the velocity of the blood. The first two parameters can be determined by imaging spectrometry at the patients ocular fundus. However, the reflected light emerging from a vessel followed different pathways through the ocular fundus layers and the vessel embedded in the retina. The contribution of the single pathways to the vessel reflection profile is investigated by a Monte Carlo simulation. Considering retinal vessels with diameters of 25-200 microm we found the reflection from a thin vessel to be determined by the single and double transmission of light at 560 nm. The backscattering from the blood column determines the reflectance in the case of a thick vessel. However, both components are in the same order of magnitude. This has to be considered in the calculation of the oxygen saturation of blood in retinal vessels from their reflection spectra.

Microcell-mediated transfer of chromosome 4 into HeLa cells suppresses telomerase activity.

Telomerase activity can be detected in most human cancers and immortal cell lines. In contrast, the lack of telomerase activity in normal diploid fibroblasts has been correlated with progressive reduction of telomere lengths to critically short sizes followed by the cessation of cell division and the onset of senescence. Several investigators have provided evidence for the localization of a telomerase suppressor gene on chromosome 3. The aim of our study was to determine whether other chromosomes are involved in telomerase repression. Beside human chromosome 3 (serving as positive control), chromosomes 4, 6, and 11 were introduced into HeLa cells via microcell-mediated chromosome transfer. Telomerase activity from different hybrid cell lysates was determined at an early time point after fusion using a Telomerase ELISA kit. Strong repression of telomerase activity was only found in a subset of HeLa hybrids in which chromosome 3 or chromosome 4 had been introduced. Telomerase suppression induced by chromosome 3 or 4 transfer was paralleled by a high frequency (30% or 43%, respectively) of a senescent-like phenotype. Chromosomes 6 and 11, the functional loss of which is also implicated in cervical cancer, had no effect. These results indicate that normal human chromosomes 3 and 4 carry a gene or genes that suppress telomerase activity and induce cellular senescence in HeLa cells.

[An experimental study on the use of the Hilbert operator as a method of signal preprocessing for the determination of oxygen saturation in retinal vessels]. / Experimentelle Studie zur Anwendung des Hilbertoperators als Methode zur Signalvorverarbeitung für die Bestimmung der Sauerstoffsättigung in retinalen Gefässen.

For the non-invasive measurement of the oxygen saturation in human retinal vessels, the light reflected by a vessel and its surroundings is evaluated. Differences in the absorption and scattering properties of the optical media provide so-called vessel profiles, but the central vessel section is often disturbed by a regular reflex. In order to eliminate this reflex, a method based on the Hilbert transform is presented, which can be used for the determination of logarithmic differences between the reflected light on and that beside the vessel. The data for our investigations were produced by simulation of the radiation transport in multi-layered tissue. A linear regression between expected and measured values based on 40 pairs was used for the evaluation of the proposed method. A linear relationship was shown to exist.