Unraveling the molecular landscape of lead-induced cochlear synaptopathy: a quantitative proteomics analysis.

cochlear synaptopathy cochlear synaptosomes hearing loss lead-induced ototoxicity synaptic vesicle cycle

Journal

Frontiers in cellular neuroscience
ISSN: 1662-5102
Titre abrégé: Front Cell Neurosci
Pays: Switzerland
ID NLM: 101477935

Informations de publication

Date de publication:
2024
Historique:
received: 27 03 2024
accepted: 03 07 2024
medline: 6 8 2024
pubmed: 6 8 2024
entrez: 6 8 2024
Statut: epublish

Résumé

Exposure to heavy metal lead can cause serious health effects such as developmental neurotoxicity in infants, cognitive impairment in children, and cardiovascular and nephrotoxic effects in adults. Hearing loss is one of the toxic effects induced by exposure to lead. Previous studies demonstrated that exposure to lead causes oxidative stress in the cochlea and disrupts ribbon synapses in the inner hair cells. This study investigated the underlying mechanism by evaluating the changes in the abundance of cochlear synaptosomal proteins that accompany lead-induced cochlear synaptopathy and hearing loss in mice. Young-adult CBA/J mice were given lead acetate in drinking water for 28 days. Lead exposure significantly increased the hearing thresholds, particularly at the higher frequencies in both male and female mice, but it did not affect the activity of outer hair cells or induce hair cell loss. However, lead exposure decreased wave-I amplitude, suggesting lead-induced cochlear synaptopathy. In agreement, colocalization of pre- and post-synaptic markers indicated that lead exposure decreased the number of paired synapses in the basal turn of the cochlea. Proteomics analysis indicated that lead exposure increased the abundance of 352 synaptic proteins and decreased the abundance of 394 synaptic proteins in the cochlea. Bioinformatics analysis indicated that proteins that change in abundance are highly enriched in the synaptic vesicle cycle pathway. Together, these results suggest that outer hair cells are not the primary target in lead-induced ototoxicity, that lead-induced cochlear synaptopathy is more pronounced in the basal turn of the cochlea, and that synaptic vesicle cycle signaling potentially plays a critical role in lead-induced cochlear synaptopathy.

Identifiants

pubmed: 39104440
doi: 10.3389/fncel.2024.1408208
pmc: PMC11298392
doi:

Types de publication

Journal Article

Langues

eng

Pagination

1408208

Informations de copyright

Copyright © 2024 Bhatia, Mehmood, Doyon-Reale, Rosati, Stemmer and Jamesdaniel.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Auteurs

Pankaj Bhatia (P)

Institute of Environmental Health Sciences, Wayne State University, Detroit, MI, United States.

Shomaila Mehmood (S)

Institute of Environmental Health Sciences, Wayne State University, Detroit, MI, United States.

Nicole Doyon-Reale (N)

Institute of Environmental Health Sciences, Wayne State University, Detroit, MI, United States.

Rita Rosati (R)

Institute of Environmental Health Sciences, Wayne State University, Detroit, MI, United States.

Paul M Stemmer (PM)

Institute of Environmental Health Sciences, Wayne State University, Detroit, MI, United States.

Samson Jamesdaniel (S)

Institute of Environmental Health Sciences, Wayne State University, Detroit, MI, United States.
Department of Family Medicine and Public Health Sciences, Wayne State University, Detroit, MI, United States.

Classifications MeSH