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Biomedical subjects

André J Noest

Publications and source records attributed to André J Noest.

2 recordsLinked to original sources

The time course of binocular rivalry reveals a fundamental role of noise.

When our two eyes view incongruent images, we experience binocular rivalry: An ongoing cycle of dominance periods of either image and transition periods when both are visible. Two key forces underlying this process are adaptation of and inhibition between the images' neural representations. Models based on these factors meet the constraints posed by data on dominance periods, but these are not very stringent. We extensively studied contrast dependence of dominance and transition durations and that of the occurrence of return transitions: Occasions when an eye loses and regains dominance without intervening dominance of the other eye. We found that dominance durations and the incidence of return transitions depend similarly on contrast; transition durations show a different dependence. Regarding dominance durations, we show that the widely accepted rule known as Levelt's second proposition is only valid in a limited contrast range; outside this range, the opposite of the proposition is true. Our data refute current models, based solely on adaptation and inhibition, as these cannot explain the long and reversible transitions that we find. These features indicate that noise is a crucial force in rivalry, frequently dominating the deterministic forces.

Adaptation, Physiological↗

Thymic selection does not limit the individual MHC diversity.

The number of different major histocompatibility (MHC) molecules expressed per individual is widely believed to represent a trade-off between maximizing the detection of foreign antigens, and minimizing the loss of T cell clones due to self-tolerance induction. Using a mathematical model we here show that this argument fails to explain why individuals typically express of the order of 1020 different MHC molecules. Expression of extra MHC types decreases the number of clones surviving negative selection, but increases the number of positively selected clones. Based on experimental parameter estimates, we show that the number of clones in the functional T cell repertoire would in fact increase if the MHC diversity within an individual were to exceed its normal value, until more than one hundred different MHC molecules would be expressed. Since additional MHC types also increase the number of presented pathogen peptides, resistance against pathogens only decreases at unrealistically high MHC diversities exceeding 1,500 different MHC molecules per individual.

Animals↗