Abstract
The cerebral cortex is organized in vertical columns that contain neurons with similar functions. The cellular micro-architecture of such columns is an essential determinant of brain dynamics and cortical information processing. However, a detailed understanding of columns is incomplete, even in the best studied cortical regions, and mostly restricted to the upper cortical layers. Here, we developed a two-photon Ca 2+ -imaging-based method for the serial functional mapping of all pyramidal layers of the mouse primary auditory cortex at single-neuron resolution in individual animals. We demonstrate that the best frequency-responsive neurons are organized in all-layers-crossing narrow columns, with fuzzy boundaries and a bandwidth of about one octave. This micro-architecture is, in many ways, different from what has been reported before, indicating the region and stimulus specificity of functional cortical columns in vivo. Tischbirek et al. report a two-photon Ca 2+ -imaging-based approach to map sensory-evoked neuronal activity from L2/3 to L6 of mouse cortex. In the primary auditory cortex, the authors identify functional microcolumns at cellular resolution that bring together large-scale tonotopy and locally heterogeneous frequency responses throughout all cortical layers.
Original language | English |
---|---|
Pages (from-to) | 1319-1326.e5 |
Journal | Cell Reports |
Volume | 27 |
Issue number | 5 |
DOIs | |
State | Published - 30 Apr 2019 |
Keywords
- calcium imaging
- cellular micro-architecture
- cortical column
- cortical layers
- mouse auditory cortex
- tonotopy
- two-photon microscopy
All Science Journal Classification (ASJC) codes
- General Biochemistry,Genetics and Molecular Biology