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1.
Elife ; 72018 12 18.
Artículo en Inglés | MEDLINE | ID: mdl-30561325

RESUMEN

It is generally assumed that human intelligence relies on efficient processing by neurons in our brain. Although grey matter thickness and activity of temporal and frontal cortical areas correlate with IQ scores, no direct evidence exists that links structural and physiological properties of neurons to human intelligence. Here, we find that high IQ scores and large temporal cortical thickness associate with larger, more complex dendrites of human pyramidal neurons. We show in silico that larger dendritic trees enable pyramidal neurons to track activity of synaptic inputs with higher temporal precision, due to fast action potential kinetics. Indeed, we find that human pyramidal neurons of individuals with higher IQ scores sustain fast action potential kinetics during repeated firing. These findings provide the first evidence that human intelligence is associated with neuronal complexity, action potential kinetics and efficient information transfer from inputs to output within cortical neurons.


Asunto(s)
Encéfalo/fisiología , Inteligencia , Células Piramidales/fisiología , Potenciales de Acción , Adolescente , Adulto , Anciano , Simulación por Computador , Femenino , Humanos , Pruebas de Inteligencia , Masculino , Persona de Mediana Edad , Modelos Neurológicos , Adulto Joven
2.
Elife ; 52016 10 06.
Artículo en Inglés | MEDLINE | ID: mdl-27710767

RESUMEN

The advanced cognitive capabilities of the human brain are often attributed to our recently evolved neocortex. However, it is not known whether the basic building blocks of the human neocortex, the pyramidal neurons, possess unique biophysical properties that might impact on cortical computations. Here we show that layer 2/3 pyramidal neurons from human temporal cortex (HL2/3 PCs) have a specific membrane capacitance (Cm) of ~0.5 µF/cm2, half of the commonly accepted 'universal' value (~1 µF/cm2) for biological membranes. This finding was predicted by fitting in vitro voltage transients to theoretical transients then validated by direct measurement of Cm in nucleated patch experiments. Models of 3D reconstructed HL2/3 PCs demonstrated that such low Cm value significantly enhances both synaptic charge-transfer from dendrites to soma and spike propagation along the axon. This is the first demonstration that human cortical neurons have distinctive membrane properties, suggesting important implications for signal processing in human neocortex.


Asunto(s)
Potenciales de Acción/fisiología , Membrana Celular/fisiología , Potenciales Postsinápticos Excitadores/fisiología , Modelos Neurológicos , Neocórtex/fisiología , Células Piramidales/fisiología , Adulto , Anciano de 80 o más Años , Animales , Axones/fisiología , Axones/ultraestructura , Membrana Celular/ultraestructura , Dendritas/fisiología , Dendritas/ultraestructura , Femenino , Humanos , Masculino , Ratones , Microtomía , Persona de Mediana Edad , Neocórtex/citología , Técnicas de Placa-Clamp , Células Piramidales/ultraestructura , Lóbulo Temporal/citología , Lóbulo Temporal/fisiología
3.
Commun Integr Biol ; 4(4): 486-8, 2011 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-21966579

RESUMEN

Despite a long history of anatomical mapping of neuronal networks, we are only beginning to understand the detailed three-dimensional (3D) organization of the cortical micro-circuitry. This is in part due to the lack of complete reconstructions of individual cortical neurons. Morphological studies are either performed on incomplete cells in vitro, or when performed in vivo, lack the necessary cellular resolution. We recently reconstructed the in vivo axonal and dendritic morphology of two types of L(ayer) 5 neurons from vibrissal cortex. The 3D profiles of short-range as well as longrange projections indicate that L5 slender-tufted and L5 thick-tufted neurons represent very different building blocks of the cortical circuitry. In this addendum to Oberlaender et al. (PNAS 2011), we motivate our technical approach and the advancements this may give in reconstructing the cortical micro-circuitry.

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