Summary
Saccharomyces cerevisiae responds to environ‐mental stimuli such as an exposure
to pheromone or to hexoses after carbon source limitation with a transient elevation
of cytosolic calcium (TECC) response. In this study, we examined whether hexose transport
and phosphorylation are necessary for the TECC response. We found that a mutant strain
lacking most of the known hexose transporters was unable to carry out the TECC response
when exposed to glucose. A mutant strain that lacked the ability to phosphorylate
glucose was unable to respond to glucose addition, but displayed a normal TECC response
after the addition of galactose. These results indicate that hexose uptake and phosphorylation
are required to trigger the hexose‐induced TECC response. We also found that the
TECC response was significantly smaller than normal when the level of environmental
calcium was reduced, and was abolished in a mid1 mutant that lacked a subunit of the high‐affinity calcium channel of the yeast plasma membrane. These results indicate that most or all of the TECC response is mediated by an influx of calcium from the extracellular space. Our results indicate that this transient increase in plasma membrane calcium permeability may be linked to the accumulation of Glc‐1‐P (or a related glucose metabolite) in yeast.
The measurement of CD42a- and PAC1-positive microparticles may provide important additional information which can help to improve the early instalment of antifungal therapy of severe septic patients.
Genetic variants in CYP2C19 have a gene-dose effect on post-clopidogrel platelet reactivity, with homozygote LOF carriers having the highest risk for HTPR and for adverse ischemic events. Neither ABCB1 nor PON-1 genotypes significantly influenced platelet reactivity or outcome.
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