Poster Session 3.N - Neurosciences
Tóth, Katalin Zsófia
Hun-Ren Research Centre for Natural Sciences
Katalin Zsófia Tóth1, Réka Bod1, Yossef Michaeli2, Orsolya Farkas3, Loránd Erőss4, László Entz4, Dániel Fabó4, István Ulbert1, Kinga Tóth1, Lucia Wittner1
1: HUN-REN Research Centre for Natural Sciences
2: Semmelweis University
3: Péter Pázmány Catholic University
4: Semmelweis University Clinics of Neurosurgery and Neurointervention
Introduction
Our understanding of how cortical microstructure relates to neuronal firing in the human brain remains limited, particularly across layers.
Aims
To investigate layer-specific relationships between neuronal density, inhibitory interneuron organization, and firing dynamics using combined in vivo and in vitro recordings.
Methods
Chronic intracortical recordings were obtained in vivo during wakefulness and sleep. Following surgical resection, acute in vitro recordings were performed on adjacent cortical tissue using identical 24-channel linear arrays (150 µm spacing). Histological analyses were conducted on tissue near in vivo recording sites and from distal regions used in vitro. Neuronal density was quantified using NeuN immunohistochemistry. Parvalbumin (PV) interneurons were additionally assessed for density and coverage (percentage area).
Results
NeuN-positive density was higher in supragranular than infragranular layers. In vivo, higher supragranular density was associated with increased firing rates, reduced burstiness, and more regular firing, whereas infragranular layers showed the opposite pattern. In vitro, these relationships were weaker, although supragranular density remained predictive. PV interneuron analysis revealed layer-dependent differences in inhibitory density and coverage. In patients with paired datasets, supragranular physiology was consistently predicted by anatomical measures, while infragranular in vivo activity was better explained by locally sampled anatomy.
Conclusion
Structure–function relationships in the human cortex are layer-dependent and differ between in vivo and in vitro conditions, shaped by both neuronal density and inhibitory organization.
Funding
This project was supported by the SE 250+ Excellence PhD Scholarship, the Hungarian Brain Research Program (NAP2022-I-2/2022), and the Pharmaceutical Research and Development Laboratory Project (PharmaLab, RRF-2.3.1-21-2022-00015). This work was further supported by OTKA K137886 and Advanced 150799.