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AMP‐activated protein kinase in BK‐channel regulation and protection against hearing loss following acoustic overstimulation
Author(s) -
Föller Michael,
Jaumann Mirko,
Dettling Juliane,
Saxena Ambrish,
Pakladok Tatsiana,
Munoz Carlos,
Ruth Peter,
Sopjani Mentor,
Seebohm Guiscard,
Rüttiger Lukas,
Knipper Marlies,
Lang Florian
Publication year - 2012
Publication title -
the faseb journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.709
H-Index - 277
eISSN - 1530-6860
pISSN - 0892-6638
DOI - 10.1096/fj.12-208132
Subject(s) - stimulation , audiology , hearing loss , chemistry , medicine
The energy‐sensing AMP‐activated serine/threonine protein kinase (AMPK) confers cell survival in part by stimulation of cellular energy production and limitation of cellular energy utilization. AMPK‐sensitive functions further include activities of epithelial Na + channel ENaC and voltage‐gated K + channel KCNE1/KCNQ1. AMPK is activated by an increased cytosolic Ca 2+ concentration. The present study explored whether AMPK regulates the Ca 2+ ‐sensitive large conductance and voltage‐gated potassium (BK) channel. cRNA encoding BK channel was injected into Xenopus oocytes with and without additional injection of wild‐type AMPK (AMPKα1+AMPKβ1+AMPKγ1), constitutively active AMPK γR70Q , or inactive AMPK αK45R . BK‐channel activity was determined utilizing the 2‐electrode voltage‐clamp. Moreover, BK‐channel protein abundance in the cell membrane was determined by confocal immunomicroscopy. As BK channels are expressed in outer hair cells (OHC) of the inner ear and lack of BK channels increases noise vulnerability, OHC BK‐channel expression was examined by immunohistochemistry and hearing function analyzed by auditory brain stem response measurements in AMPK α 1‐deficient mice ( ampk –/– ) and in wild‐type mice ( ampk +/+ ). As a result, coexpression of AMPK or AMPK γR70Q but not of AMPK αK45R significantly enhanced BK‐channel‐mediated currents and BK‐channel protein abundance in the oocyte cell membrane. BK‐channel expression in the inner ear was lower in ampk –/– mice than in ampk +/+ mice. The hearing thresholds prior to and immediately after an acoustic overexposure were similar in ampk –/– and ampk +/+ mice. However, the recovery from the acoustic trauma was significantly impaired in ampk –/– mice compared to ampk +/+ mice. In summary, AMPK is a potent regulator of BK channels. It may thus participate in the signaling cascades that protect the inner ear from damage following acoustic overstimulation.—Föller, M., Jaumann, M., Dettling, J., Saxena, A., Pakladok, T., Munoz, C., Ruth, P., Sopjani, M., Seebohm, G., Rüttiger, L., Knipper, M., Lang, F. AMP‐activated protein kinase in BK‐channel regulation and protection against hearing loss following acoustic overstimulation. FASEB J. 26, 4243–4253 (2012). www.fasebj.org