Application of the direct beta counter Matrix 96 for cytotoxic assays: Simultaneous processing and reading of 96 wells using a51Cr-retention assay

To assess the cytotoxic activity of immune cells, we have developed a⁵¹Cr-retention assay in which the radioactivity retained by⁵¹Cr-labeled target cells, following coincubation with cytotoxic cells, is monitored using the automated Matrix 96 beta counter. The Matrix 96 is designed for simultaneously counting 96 samples isolated from a 96-well microplate. It uses 96 uniform and independent detectors operating on the principle of avalanche gas ionization in the Geiger-Muller mode. Samples must be dry because the detectors are of the open-window type. Therefore, samples from the 96 wells of the microplate are simultaneously harvested onto a filter using the MicroMate 196, a 96-well cell harvester, dried and quantified in the Matrix 96. Usually the⁵¹Cr isotope is measured by the detection of gamma radiation in gamma counters. The Matrix 96, however, monitors Auger electrons, which are also emitted by⁵¹Cr. We have shown that the retention assay can be used to monitor the cytotoxic activity of activated lymphocytes including lymphokine-activated killer cells and tumor-infiltrating lymphocytes against various tumor cell lines. This assay is most suitable for experiments in which low E/T ratios are sufficient to detect highly cytotoxic cells, such as clone screening in cloning assays or in limiting-dilution analysis assays. These assays involve processing and reading large numbers of microplates. In this case, the retention assay monitored in the Matrix 96 will improve the work flow and decrease the amount of radioactive waste.This work was supported by the American Cancer Society grant IN-162-C     

Spatial relations between shrubs and Prosopis glandulosa canopies

Abstract. Prosopis glandulosa, an arborescent legume, may act as a nurse plant that facilitates the establishment of other woody species. We hypothesized that attenuation of radiant energy and increased soil nutrients beneath P. glandulosa canopies facilitate establishment of subordinate shrubs and shrub cluster development. We determined the spatial distribution pattern of shrubs under P. glandulosa at three locations in southern Texas. Density of Celtis pallida, Zanthoxylum fagara, and total woody plants were comparable among the four cardinal directions at each location, which countered the prediction that shrub density would be greater on the north side of P. glandulosa canopies if attenuation of solar energy was a factor in cluster development. Total woody plant density increased with increasing P. glandulosa basal diameter, canopy radius, and height only at one location. Total woody plant density decreased with increasing total N in the upper 15 cm of soil at two of the three locations. Late in shrub cluster development, extraction of N from the soil and incorporation of N into plant tissue in dense shrub clusters may operate to inhibit further increases in subordinate shrub density.