Immunological characterization of two types of ionocytes in the inner ear epithelium of Pacific Chub Mackerel (Scomber japonicus)

The inner ear is essential for maintaining balance and hearing predator and prey in the environment. Each inner ear contains three CaCO 3 otolith polycrystals, which are calcified within an alkaline, K + -rich endolymph secreted by the surrounding epithelium. However, the underlying cellular mechani...

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Published inJournal of comparative physiology. B, Biochemical, systemic, and environmental physiology Vol. 190; no. 4; pp. 419 - 431
Main Authors Kwan, Garfield T., Smith, Taylor R., Tresguerres, Martin
Format Journal Article
LanguageEnglish
Published Berlin/Heidelberg Springer Berlin Heidelberg 01.07.2020
Springer Nature B.V
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Summary:The inner ear is essential for maintaining balance and hearing predator and prey in the environment. Each inner ear contains three CaCO 3 otolith polycrystals, which are calcified within an alkaline, K + -rich endolymph secreted by the surrounding epithelium. However, the underlying cellular mechanisms are poorly understood, especially in marine fish. Here, we investigated the presence and cellular localization of several ion-transporting proteins within the saccular epithelium of the Pacific Chub Mackerel ( Scomber japonicus ). Western blotting revealed the presence of Na + /K + -ATPase (NKA), carbonic anhydrase (CA), Na + -K + -2Cl − -co-transporter (NKCC), vacuolar-type H + -ATPase (VHA), plasma membrane Ca 2+ ATPase (PMCA), and soluble adenylyl cyclase (sAC). Immunohistochemistry analysis identified two distinct ionocytes types in the saccular epithelium: Type-I ionocytes were mitochondrion-rich and abundantly expressed NKA and NKCC in their basolateral membrane, indicating a role in secreting K + into the endolymph. On the other hand, Type-II ionocytes were enriched in cytoplasmic CA and VHA, suggesting they help transport HCO 3 − into the endolymph and remove H + . In addition, both types of ionocytes expressed cytoplasmic PMCA, which is likely involved in Ca 2+ transport and homeostasis, as well as sAC, an evolutionary conserved acid–base sensing enzyme that regulates epithelial ion transport. Furthermore, CA, VHA, and sAC were also expressed within the capillaries that supply blood to the meshwork area, suggesting additional mechanisms that contribute to otolith calcification. This information improves our knowledge about the cellular mechanisms responsible for endolymph ion regulation and otolith formation, and can help understand responses to environmental stressors such as ocean acidification.
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ISSN:0174-1578
1432-136X
DOI:10.1007/s00360-020-01276-3