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Jose-Manuel Alonso

Publications and source records attributed to Jose-Manuel Alonso.

4 recordsLinked to original sources

Functionally distinct inhibitory neurons at the first stage of visual cortical processing.

Here we explore inhibitory circuits at the thalamocortical stage of processing in layer 4 of the cat's visual cortex, focusing on the anatomy and physiology of the interneurons themselves. Our immediate aim was to explore the inhibitory mechanisms that contribute to orientation selectivity, perhaps the most dramatic response property to emerge across the thalamocortical synapse. The broader goal was to understand how inhibitory circuits operate. Using whole-cell recording in cats in vivo, we found that layer 4 contains two populations of inhibitory cells defined by receptive field class--simple and complex. The simple cells were selective for stimulus orientation, whereas the complex cells were not. Our observations help to explain how neurons become sensitive to stimulus orientation and maintain that selectivity as stimulus contrast changes. Overall, the work suggests that different sources of inhibition, either selective for specific features or broadly tuned, interact to provide appropriate representations of elements within the environment.

Animals↗

Two different types of Y cells in the cat lateral geniculate nucleus.

The Y pathway in the cat visual system is traditionally viewed as a single channel that originates in the retina. However, most Y cells from the contralateral retina diverge to innervate two different layers of the lateral geniculate nucleus, suggesting a possible channel split: YC (Y geniculate cell in layer C) and YA (Y geniculate cell in layer A). We tested the functional significance of this anatomical divergence by comparing the response properties of simultaneously recorded YC and YA geniculate cells with overlapping receptive fields. Our results demonstrate that YC and YA cells significantly differ in a large number of temporal and spatial parameters including response latency, response transiency, receptive-field size, and linearity of spatial summation. Furthermore, for some of these parameters, the differences between YC and YA cells are as pronounced as the differences between Y and X cells in layer A. These results along with results from previous studies strongly suggest that Y retinal afferents diverge into two separate channels at the level of the thalamus.

Action Potentials↗

Complex receptive fields in primary visual cortex.

In the early 1960s, Hubel and Wiesel reported the first physiological description of cells in cat primary visual cortex. They distinguished two main cell types: simple cells and complex cells. Based on their distinct response properties, they suggested that the two cell types could represent two consecutive stages in receptive-field construction. Since the 1960s, new experimental and computational evidence provided serious alternatives to this hierarchical model. Parallel models put forward the idea that both simple and complex receptive fields could be built in parallel by direct geniculate inputs. Recurrent models suggested that simple cells and complex cells may not be different cell types after all. To this day, a consensus among hierarchical, parallel, and recurrent models has been difficult to attain; however, the circuitry used by all models is becoming increasingly similar. The authors review theoretical and experimental evidence for each line of models emphasizing their strengths and weaknesses.

Animals↗

Neural connections and receptive field properties in the primary visual cortex.

A cubic millimeter of primary visual cortex contains about 100,000 neurons that are heavily interconnected by intrinsic and extrinsic afferents. The effort of many neuroanatomists over the past has revealed the general outline of these connections; however, their function remains a mystery. Recently, combined physiological and anatomical approaches are beginning to reveal the role of these connections in the generation of cortical receptive fields. A common theme emerges from all these studies: cortical connections are remarkably specific and this specificity is determined in great extent by the type of connection and the neuronal response properties. Feedforward connections follow relatively rigid rules of wiring selectively targeting neurons with receptive fields matched in position and contrast polarity (thalamus --> cortical layer 4) or position and orientation selectivity (layer 4 --> layers 2 + 3). In contrast, horizontal connections follow more flexible rules connecting distant cells that are not retinotopically aligned and neighboring cells with different orientation preferences. These differences in connectivity may give a hint on how visual stimuli are processed in the primary visual cortex. An attractive hypothesis is that local stimuli use the highly selective feedforward inputs to reliably drive cortical neurons while background stimuli modulate their activity through more flexible horizontal (and feedback) connections.

Animals↗