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Suppressed expression of LDHB promotes age-related hearing loss via aerobic glycolysis.

Chunjie TianYeon Ju KimSai HaliOak-Sung ChooJin-Sol LeeSeo-Kyung JungYoun-Uk ChoiChan Bae ParkYun-Hoon Choung
Published in: Cell death & disease (2020)
Age-dependent decrease of mitochondrial energy production and cellular redox imbalance play significant roles in age-related hearing loss (ARHL). Lactate dehydrogenase B (LDHB) is a key glycolytic enzyme that catalyzes the interconversion of pyruvate and lactate. LDH activity and isoenzyme patterns are known to be changed with aging, but the role of LDHB in ARHL has not been studied yet. Here, we found that LDHB knockout mice showed hearing loss at high frequencies, which is the typical feature of ARHL. LDHB knockdown caused downregulation of mitochondrial functions in auditory cell line, University of Bristol/organ of Corti 1 (UB/OC1) with decreased NAD+ and increased hypoxia inducing factor-1α. LDHB knockdown also enhanced the death of UB/OC1 cells with ototoxic gentamicin treatment. On the contrary, the induction of LDHB expression caused enhanced mitochondrial functions, including changes in mitochondrial respiratory subunits, mitochondrial membrane potentials, ATP, and the NAD+/NADH ratio. Thus, we concluded that suppression of LDHB activity may be closely related with the early onset or progression of ARHL.
Keyphrases
  • hearing loss
  • early onset
  • oxidative stress
  • poor prognosis
  • late onset
  • cell proliferation
  • signaling pathway
  • cell cycle arrest
  • deep learning
  • cell death
  • working memory
  • combination therapy
  • long non coding rna