Neurophysiology of the macaque fronto-parietal magnitude system

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Aufrufstatistik

URI: http://hdl.handle.net/10900/82646
http://nbn-resolving.de/urn:nbn:de:bsz:21-dspace-826467
http://dx.doi.org/10.15496/publikation-24037
Dokumentart: Dissertation
Date: 2020-04-28
Language: English
Faculty: 7 Mathematisch-Naturwissenschaftliche Fakultät
Department: Biologie
Advisor: Nieder, Andreas (Prof. Dr.)
Day of Oral Examination: 2018-04-27
DDC Classifikation: 570 - Life sciences; biology
Keywords: Nervenzelle , Zahlensystem , Gehirn , Primaten , Exekutive Funktionen , Elektrophysiologie
Other Keywords: Zahlen
rezeptives Feld
Präfrontalkortex
hintere Parietalrinde
non-human primate
prefrontal cortex
parietal cortex
numerosity
receptive field
License: Publishing license excluding print on demand
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Inhaltszusammenfassung:

Dissertation ist gesperrt bis 27. April 2020 !

Abstract:

In primates, the magnitude system resides in a fronto-parietal network. Single neurons in the monkey prefrontal cortex (PFC) and ventral intraparietal area (VIP) exhibit higher responses to a certain number of stimulus items regardless of their appearance or even sensory modality. Neuroimaging studies in humans show corresponding activation in human fronto-parietal areas during enumeration tasks. However, these areas are also involved in many other executive functions and, thus, the responses of single neurons within the network could be shaped by many factors. Understanding how information about magnitude develops within single neurons in this network was the objective of this thesis. This thesis includes five studies addressing various aspects of the primate frontoparietal magnitude system. First, we determined the role of behavioural relevance in shaping neuronal responses to number. Using enumerable coloured stimuli that naïve macaque monkeys discriminated based on their colour rather than number, we examined the selectivity of neuronal responses towards the number of stimuli. We simultaneously recorded single neurons in VIP and PFC. We compared these neurons to those recorded after a period of training for both monkeys, while they discriminated the stimuli based on number. In all the recording sessions, we also mapped the visual receptive fields (RF) of neurons using a passive fixation task. We created RF maps for a large number of spatially-selective neurons in each area and compared the RFs of pairs of neurons recorded at the same electrode tip. We then differentiated the extent of interaction between the RF and number selectivity in both areas. Neurons in both PFC and VIP were selective for number despite the monkeys being numerically-naïve and number being the behaviourally irrelevant stimulus feature. Post training, neurons in PFC were modulated by behavioural relevance and their selectivity for number became stronger as a result. VIP neurons did not show such an effect. We found that PFC RFs were predominantly contralateral and VIP RFs, foveal. Regardless of RF location and size, we observed heterogeneous and sometimes, inverted RFs in neurons adjacent to each other, more frequently in PFC than in VIP. Lastly, neurons in both PFC and VIP were strongly number-selective even when the number stimuli were shown outside their RFs. Our results provided valuable insight into the organisation of the magnitude system in primates. The presence of number-selective neuronal responses in numerically-naïve monkeys even when the number of stimuli was behaviourally irrelevant confirmed that our magnitude system processes magnitude spontaneously as a natural category. The strict spatiotopic organisation of RFs characteristic of early visual areas is progressively lower in VIP and PFC. Together, these results point to a hierarchy in the fronto-parietal areas we studied, with PFC located at the apex of the magnitude system and VIP upstream to it.

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