Table 1_cAMP-MFN2 signaling suppresses cochlear cell senescence and age-related hearing loss.xlsx

Introduction<p>Age-related hearing loss (presbycusis) is the most common sensory deficit in the elderly, yet it lacks effective pharmacological treatments. The decline of the cyclic AMP (cAMP) signaling pathway is implicated in aging, but its functional role in the auditory system remains larg...

Description complète

Enregistré dans:
Détails bibliographiques
Auteur principal: Yu Liu (6938) (author)
Autres auteurs: Jinyuan Cao (11506260) (author), Jie Cui (198388) (author), Haitong Chen (20830751) (author), Shujing Qin (11862449) (author), Qi Li (67548) (author), Zhongwu Su (499868) (author)
Publié: 2025
Sujets:
Tags: Ajouter un tag
Pas de tags, Soyez le premier à ajouter un tag!
_version_ 1849927624277622784
author Yu Liu (6938)
author2 Jinyuan Cao (11506260)
Jie Cui (198388)
Haitong Chen (20830751)
Shujing Qin (11862449)
Qi Li (67548)
Zhongwu Su (499868)
author2_role author
author
author
author
author
author
author_facet Yu Liu (6938)
Jinyuan Cao (11506260)
Jie Cui (198388)
Haitong Chen (20830751)
Shujing Qin (11862449)
Qi Li (67548)
Zhongwu Su (499868)
author_role author
dc.creator.none.fl_str_mv Yu Liu (6938)
Jinyuan Cao (11506260)
Jie Cui (198388)
Haitong Chen (20830751)
Shujing Qin (11862449)
Qi Li (67548)
Zhongwu Su (499868)
dc.date.none.fl_str_mv 2025-11-26T05:15:19Z
dc.identifier.none.fl_str_mv 10.3389/fimmu.2025.1715738.s003
dc.relation.none.fl_str_mv https://figshare.com/articles/dataset/Table_1_cAMP-MFN2_signaling_suppresses_cochlear_cell_senescence_and_age-related_hearing_loss_xlsx/30717773
dc.rights.none.fl_str_mv CC BY 4.0
info:eu-repo/semantics/openAccess
dc.subject.none.fl_str_mv Genetic Immunology
age-related hearing loss (ARHL)
cAMP
mitofusin2
mitochondrial dynamics
inflammation
dc.title.none.fl_str_mv Table 1_cAMP-MFN2 signaling suppresses cochlear cell senescence and age-related hearing loss.xlsx
dc.type.none.fl_str_mv Dataset
info:eu-repo/semantics/publishedVersion
dataset
description Introduction<p>Age-related hearing loss (presbycusis) is the most common sensory deficit in the elderly, yet it lacks effective pharmacological treatments. The decline of the cyclic AMP (cAMP) signaling pathway is implicated in aging, but its functional role in the auditory system remains largely unknown.</p>Methods<p>To investigate whether enhancing cAMP signaling could counteract presbycusis and elucidate the underlying molecular mechanism, we used a D-galactose-induced cellular senescence model and an in vivo aged mouse model. The effects of the cAMP analog dibutyryl-cAMP (dbcAMP) on cellular senescence, inflammation, mitochondrial function, and cochlear structure were evaluated. The role of Mitofusin-2 (MFN2) was further assessed using siRNA-mediated knockdown.</p>Results<p>dbcAMP potently suppressed cellular senescence and the associated inflammatory phenotype. In addition, cAMP treatment alleviated mitochondrial dysfunction, as indicated by improved mitochondrial bioenergetics and morphology. The anti-senescence effects of cAMP were significantly blunted upon siRNA-mediated knockdown of Mfn2, establishing MFN2 as a key, though perhaps not the sole, component of this protective pathway. Importantly, systemic administration of dbcAMP to aged mice significantly preserved hearing function and protected cochlear hair cells. This in vivo protection was accompanied by an upregulation of cochlear MFN2 and a coordinated suppression of senescence and inflammation markers.</p>Discussion<p>Our study reveals a critical protective role for the cAMP-MFN2 axis in auditory aging by suppressing cellular senescence. These findings identify this axis as a novel and promising therapeutic target for the treatment of age-related hearing loss.</p>
eu_rights_str_mv openAccess
id Manara_d26506e0f922a58fb0ddef88291ef9c9
identifier_str_mv 10.3389/fimmu.2025.1715738.s003
network_acronym_str Manara
network_name_str ManaraRepo
oai_identifier_str oai:figshare.com:article/30717773
publishDate 2025
repository.mail.fl_str_mv
repository.name.fl_str_mv
repository_id_str
rights_invalid_str_mv CC BY 4.0
spelling Table 1_cAMP-MFN2 signaling suppresses cochlear cell senescence and age-related hearing loss.xlsxYu Liu (6938)Jinyuan Cao (11506260)Jie Cui (198388)Haitong Chen (20830751)Shujing Qin (11862449)Qi Li (67548)Zhongwu Su (499868)Genetic Immunologyage-related hearing loss (ARHL)cAMPmitofusin2mitochondrial dynamicsinflammationIntroduction<p>Age-related hearing loss (presbycusis) is the most common sensory deficit in the elderly, yet it lacks effective pharmacological treatments. The decline of the cyclic AMP (cAMP) signaling pathway is implicated in aging, but its functional role in the auditory system remains largely unknown.</p>Methods<p>To investigate whether enhancing cAMP signaling could counteract presbycusis and elucidate the underlying molecular mechanism, we used a D-galactose-induced cellular senescence model and an in vivo aged mouse model. The effects of the cAMP analog dibutyryl-cAMP (dbcAMP) on cellular senescence, inflammation, mitochondrial function, and cochlear structure were evaluated. The role of Mitofusin-2 (MFN2) was further assessed using siRNA-mediated knockdown.</p>Results<p>dbcAMP potently suppressed cellular senescence and the associated inflammatory phenotype. In addition, cAMP treatment alleviated mitochondrial dysfunction, as indicated by improved mitochondrial bioenergetics and morphology. The anti-senescence effects of cAMP were significantly blunted upon siRNA-mediated knockdown of Mfn2, establishing MFN2 as a key, though perhaps not the sole, component of this protective pathway. Importantly, systemic administration of dbcAMP to aged mice significantly preserved hearing function and protected cochlear hair cells. This in vivo protection was accompanied by an upregulation of cochlear MFN2 and a coordinated suppression of senescence and inflammation markers.</p>Discussion<p>Our study reveals a critical protective role for the cAMP-MFN2 axis in auditory aging by suppressing cellular senescence. These findings identify this axis as a novel and promising therapeutic target for the treatment of age-related hearing loss.</p>2025-11-26T05:15:19ZDatasetinfo:eu-repo/semantics/publishedVersiondataset10.3389/fimmu.2025.1715738.s003https://figshare.com/articles/dataset/Table_1_cAMP-MFN2_signaling_suppresses_cochlear_cell_senescence_and_age-related_hearing_loss_xlsx/30717773CC BY 4.0info:eu-repo/semantics/openAccessoai:figshare.com:article/307177732025-11-26T05:15:19Z
spellingShingle Table 1_cAMP-MFN2 signaling suppresses cochlear cell senescence and age-related hearing loss.xlsx
Yu Liu (6938)
Genetic Immunology
age-related hearing loss (ARHL)
cAMP
mitofusin2
mitochondrial dynamics
inflammation
status_str publishedVersion
title Table 1_cAMP-MFN2 signaling suppresses cochlear cell senescence and age-related hearing loss.xlsx
title_full Table 1_cAMP-MFN2 signaling suppresses cochlear cell senescence and age-related hearing loss.xlsx
title_fullStr Table 1_cAMP-MFN2 signaling suppresses cochlear cell senescence and age-related hearing loss.xlsx
title_full_unstemmed Table 1_cAMP-MFN2 signaling suppresses cochlear cell senescence and age-related hearing loss.xlsx
title_short Table 1_cAMP-MFN2 signaling suppresses cochlear cell senescence and age-related hearing loss.xlsx
title_sort Table 1_cAMP-MFN2 signaling suppresses cochlear cell senescence and age-related hearing loss.xlsx
topic Genetic Immunology
age-related hearing loss (ARHL)
cAMP
mitofusin2
mitochondrial dynamics
inflammation