Early retinal deprivation crossmodally alters nascent subplate circuits and activity in the auditory cortex during the precritical period

Author:

Mukherjee Didhiti1ORCID,Xue Binghan2ORCID,Chen Chih-Ting1ORCID,Chang Minzi1ORCID,Kao Joseph P Y34ORCID,Kanold Patrick O125ORCID

Affiliation:

1. Department of Biomedical Engineering, Johns Hopkins University , Baltimore, MD 21205 , United States

2. Department of Biology, University of Maryland , College Park, MD 20742 , United States

3. Department of Physiology , Center for Biomedical Engineering and Technology, , Baltimore, MD 21201 , United States

4. University of Maryland School of Medicine , Center for Biomedical Engineering and Technology, , Baltimore, MD 21201 , United States

5. Kavli Neuroscience Discovery Institute, Johns Hopkins University , Baltimore, MD 21205 , United States

Abstract

Abstract Sensory perturbation in one modality results in the adaptive reorganization of neural pathways within the spared modalities, a phenomenon known as “crossmodal plasticity,” which has been examined during or after the classic “critical period.” Because peripheral perturbations can alter the auditory cortex (ACX) activity and functional connectivity of the ACX subplate neurons (SPNs) even before the critical period, called the precritical period, we investigated if retinal deprivation at birth crossmodally alters the ACX activity and SPN circuits during the precritical period. We deprived newborn mice of visual inputs after birth by performing bilateral enucleation. We performed in vivo widefield imaging in the ACX of awake pups during the first two postnatal weeks to investigate cortical activity. We found that enucleation alters spontaneous and sound-evoked activities in the ACX in an age-dependent manner. Next, we performed whole-cell patch clamp recording combined with laser scanning photostimulation in ACX slices to investigate circuit changes in SPNs. We found that enucleation alters the intracortical inhibitory circuits impinging on SPNs, shifting the excitation-inhibition balance toward excitation and this shift persists after ear opening. Together, our results indicate that crossmodal functional changes exist in the developing sensory cortices at early ages before the onset of the classic critical period.

Funder

National Institutes of Health

Publisher

Oxford University Press (OUP)

Subject

Cellular and Molecular Neuroscience,Cognitive Neuroscience

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