Mitogen-activated protein kinases (MAPK) p38 and c-Jun N-terminal kinases (JNKs) are activated during the cellular response to stress signals. Their activity is regulated by the MAPK-phosphatase 1 (DUSP1), a key component of the anti-inflammatory response. Stress kinases are well-described elements of the response to otic injury and the otoprotective potential of JNK inhibitors is being tested in clinical trials. In contrast, there are no studies exploring the role of DUSP1 in hearing and hearing loss. Here we show that Dusp1 expression is age-regulated in the mouse cochlea. Dusp1 gene knock-out caused premature progressive hearing loss, as confirmed by auditory evoked responses in Dusp1-/- mice. Hearing loss correlated with cell death in hair cells, degeneration of spiral neurons and increased macrophage infiltration. Dusp1-/- mouse cochleae showed imbalanced redox status and deregulated expression of cytokines. These data suggest that DUSP1 is essential for cochlear homeostasis in the response to stress during ageing.

[Usage Notes] Cochlear gene expression, MKPs and MAPK Figure1 - Source Data 1.xlsx Hearing measurements of wild type and Mkp1 deficient mice Figure2 - Source Data 1.xlsx Cochlear gene expression, cell markers Figure3 - Source Data 1.xlsx Cochlear gene expression, oxidative stress markers Figure5 - Source Data 1.xlsx Cochlear gene expression, inflammation markers Figure6 - Source Data 1.xlsx

Peer reviewed