» Articles » PMID: 34133413

Neuronal Selectivity to Complex Vocalization Features Emerges in the Superficial Layers of Primary Auditory Cortex

Overview
Journal PLoS Biol
Specialty Biology
Date 2021 Jun 16
PMID 34133413
Citations 8
Authors
Affiliations
Soon will be listed here.
Abstract

Early in auditory processing, neural responses faithfully reflect acoustic input. At higher stages of auditory processing, however, neurons become selective for particular call types, eventually leading to specialized regions of cortex that preferentially process calls at the highest auditory processing stages. We previously proposed that an intermediate step in how nonselective responses are transformed into call-selective responses is the detection of informative call features. But how neural selectivity for informative call features emerges from nonselective inputs, whether feature selectivity gradually emerges over the processing hierarchy, and how stimulus information is represented in nonselective and feature-selective populations remain open question. In this study, using unanesthetized guinea pigs (GPs), a highly vocal and social rodent, as an animal model, we characterized the neural representation of calls in 3 auditory processing stages-the thalamus (ventral medial geniculate body (vMGB)), and thalamorecipient (L4) and superficial layers (L2/3) of primary auditory cortex (A1). We found that neurons in vMGB and A1 L4 did not exhibit call-selective responses and responded throughout the call durations. However, A1 L2/3 neurons showed high call selectivity with about a third of neurons responding to only 1 or 2 call types. These A1 L2/3 neurons only responded to restricted portions of calls suggesting that they were highly selective for call features. Receptive fields of these A1 L2/3 neurons showed complex spectrotemporal structures that could underlie their high call feature selectivity. Information theoretic analysis revealed that in A1 L4, stimulus information was distributed over the population and was spread out over the call durations. In contrast, in A1 L2/3, individual neurons showed brief bursts of high stimulus-specific information and conveyed high levels of information per spike. These data demonstrate that a transformation in the neural representation of calls occurs between A1 L4 and A1 L2/3, leading to the emergence of a feature-based representation of calls in A1 L2/3. Our data thus suggest that observed cortical specializations for call processing emerge in A1 and set the stage for further mechanistic studies.

Citing Articles

Dissociable Roles of the Auditory Midbrain and Cortex in Processing the Statistical Features of Natural Sound Textures.

Peng F, Harper N, Mishra A, Auksztulewicz R, Schnupp J J Neurosci. 2024; 44(10).

PMID: 38267259 PMC: 10919253. DOI: 10.1523/JNEUROSCI.1115-23.2023.


Age-related changes in the primary auditory cortex of newborn, adults and aging bottlenose dolphins () are located in the upper cortical layers.

Graic J, Corain L, Finos L, Vadori V, Grisan E, Gerussi T Front Neuroanat. 2024; 17:1330384.

PMID: 38250022 PMC: 10796513. DOI: 10.3389/fnana.2023.1330384.


Large-scale single-neuron speech sound encoding across the depth of human cortex.

Leonard M, Gwilliams L, Sellers K, Chung J, Xu D, Mischler G Nature. 2023; 626(7999):593-602.

PMID: 38093008 PMC: 10866713. DOI: 10.1038/s41586-023-06839-2.


Adaptive mechanisms facilitate robust performance in noise and in reverberation in an auditory categorization model.

Parida S, Liu S, Sadagopan S Commun Biol. 2023; 6(1):456.

PMID: 37130918 PMC: 10154343. DOI: 10.1038/s42003-023-04816-z.


Quantitative models of auditory cortical processing.

Sadagopan S, Kar M, Parida S Hear Res. 2023; 429:108697.

PMID: 36696724 PMC: 9928778. DOI: 10.1016/j.heares.2023.108697.


References
1.
Hromadka T, DeWeese M, Zador A . Sparse representation of sounds in the unanesthetized auditory cortex. PLoS Biol. 2008; 6(1):e16. PMC: 2214813. DOI: 10.1371/journal.pbio.0060016. View

2.
Agamaite J, Chang C, Osmanski M, Wang X . A quantitative acoustic analysis of the vocal repertoire of the common marmoset (Callithrix jacchus). J Acoust Soc Am. 2015; 138(5):2906-28. PMC: 4644241. DOI: 10.1121/1.4934268. View

3.
Winter P, Funkenstein H . The effect of species-specific vocalization on the discharge of auditory cortical cells in the awake squirrel monkey. (Saimiri sciureus). Exp Brain Res. 1973; 18(5):489-504. DOI: 10.1007/BF00234133. View

4.
Chechik G, Anderson M, Bar-Yosef O, Young E, Tishby N, Nelken I . Reduction of information redundancy in the ascending auditory pathway. Neuron. 2006; 51(3):359-68. DOI: 10.1016/j.neuron.2006.06.030. View

5.
Sheinberg D, Logothetis N . Noticing familiar objects in real world scenes: the role of temporal cortical neurons in natural vision. J Neurosci. 2001; 21(4):1340-50. PMC: 6762229. View