Literature DB >> 20012478

How is the highly positive endocochlear potential formed? The specific architecture of the stria vascularis and the roles of the ion-transport apparatus.

Hiroshi Hibino1, Fumiaki Nin, Chizuru Tsuzuki, Yoshihisa Kurachi.   

Abstract

Cochlear endolymph, an extracellular solution containing 150 mM K(+), exhibits a positive potential of +80 mV. This is called the endocochlear potential (EP) and is essential for audition. The mechanism responsible for formation of the EP has been an enigma for the half century since its first measurement. A key element is the stria vascularis, which displays a characteristic tissue structure and expresses multiple ion-transport apparatus. The stria comprises two epithelial layers: a layer of marginal cells and one composed of intermediate and basal cells. Between the two layers lies an extracellular space termed the intrastrial space (IS), which is thus surrounded by the apical membranes of intermediate cells and the basolateral membranes of marginal cells. The fluid in the IS exhibits a low concentration of K(+) and a positive potential similar to the EP. We have demonstrated that the IS is electrically isolated from the neighboring extracellular fluids, perilymph, and endolymph, which allows the IS to sustain its positive potential. This IS potential is generated by K(+) diffusion across the apical membranes of intermediate cells, where inwardly rectifying Kir4.1 channels are localized. The low K(+) concentration in the IS, which is mandatory for the large K(+)-diffusion potential, is maintained by Na(+),K(+)-ATPases and Na(+),K(+),2Cl(-)-cotransporters expressed at the basolateral membranes of marginal cells. An additional K(+)-diffusion potential formed by KCNQ1/KCNE1-K(+) channels at the apical membranes of marginal cells also contributes to the EP. Therefore, the EP depends on an electrically isolated space and two K(+)-diffusion potentials in the stria vascularis.

Entities:  

Mesh:

Substances:

Year:  2009        PMID: 20012478     DOI: 10.1007/s00424-009-0754-z

Source DB:  PubMed          Journal:  Pflugers Arch        ISSN: 0031-6768            Impact factor:   3.657


  116 in total

1.  mRNA encoding 'ClC-K1, a kidney Cl(-)- channel' is expressed in marginal cells of the stria vascularis of rat cochlea: its possible contribution to Cl(-) currents.

Authors:  M Ando; S Takeuchi
Journal:  Neurosci Lett       Date:  2000-04-28       Impact factor: 3.046

2.  Compartmentalization established by claudin-11-based tight junctions in stria vascularis is required for hearing through generation of endocochlear potential.

Authors:  Shin-ichiro Kitajiri; Tatsuo Miyamoto; Akihito Mineharu; Noriyuki Sonoda; Kyoko Furuse; Masaki Hata; Hiroyuki Sasaki; Yoshiaki Mori; Takahiro Kubota; Juichi Ito; Mikio Furuse; Shoichiro Tsukita
Journal:  J Cell Sci       Date:  2004-10-01       Impact factor: 5.285

3.  Cellular localization of rat Isk protein in the stria vascularis by immunohistochemical observation.

Authors:  M Sakagami; K Fukazawa; T Matsunaga; H Fujita; N Mori; T Takumi; H Ohkubo; S Nakanishi
Journal:  Hear Res       Date:  1991-11       Impact factor: 3.208

Review 4.  Comparison of ion transport mechanisms between vestibular dark cells and strial marginal cells.

Authors:  P Wangemann
Journal:  Hear Res       Date:  1995-10       Impact factor: 3.208

5.  Novel structures in marginal and intermediate cells presumably relate to functions of apical versus basal strial strata.

Authors:  Samuel S Spicer; Bradley A Schulte
Journal:  Hear Res       Date:  2005-02       Impact factor: 3.208

6.  Targeted mutagenesis of the POU-domain gene Brn4/Pou3f4 causes developmental defects in the inner ear.

Authors:  D Phippard; L Lu; D Lee; J C Saunders; E B Crenshaw
Journal:  J Neurosci       Date:  1999-07-15       Impact factor: 6.167

7.  Mice lacking the basolateral Na-K-2Cl cotransporter have impaired epithelial chloride secretion and are profoundly deaf.

Authors:  M Flagella; L L Clarke; M L Miller; L C Erway; R A Giannella; A Andringa; L R Gawenis; J Kramer; J J Duffy; T Doetschman; J N Lorenz; E N Yamoah; E L Cardell; G E Shull
Journal:  J Biol Chem       Date:  1999-09-17       Impact factor: 5.157

8.  Altered cochlear fibrocytes in a mouse model of DFN3 nonsyndromic deafness.

Authors:  O Minowa; K Ikeda; Y Sugitani; T Oshima; S Nakai; Y Katori; M Suzuki; M Furukawa; T Kawase; Y Zheng; M Ogura; Y Asada; K Watanabe; H Yamanaka; S Gotoh; M Nishi-Takeshima; T Sugimoto; T Kikuchi; T Takasaka; T Noda
Journal:  Science       Date:  1999-08-27       Impact factor: 47.728

9.  Seizures, sensorineural deafness, ataxia, mental retardation, and electrolyte imbalance (SeSAME syndrome) caused by mutations in KCNJ10.

Authors:  Ute I Scholl; Murim Choi; Tiewen Liu; Vincent T Ramaekers; Martin G Häusler; Joanne Grimmer; Sheldon W Tobe; Anita Farhi; Carol Nelson-Williams; Richard P Lifton
Journal:  Proc Natl Acad Sci U S A       Date:  2009-03-16       Impact factor: 11.205

10.  Connexin30 (Gjb6)-deficiency causes severe hearing impairment and lack of endocochlear potential.

Authors:  Barbara Teubner; Vincent Michel; Jörg Pesch; Jürgen Lautermann; Martine Cohen-Salmon; Goran Söhl; Klaus Jahnke; Elke Winterhager; Claus Herberhold; Jean-Pierre Hardelin; Christine Petit; Klaus Willecke
Journal:  Hum Mol Genet       Date:  2003-01-01       Impact factor: 6.150

View more
  53 in total

1.  Deficiency of sphingomyelin synthase-1 but not sphingomyelin synthase-2 causes hearing impairments in mice.

Authors:  Mei-Hong Lu; Makoto Takemoto; Ken Watanabe; Huan Luo; Masataka Nishimura; Masato Yano; Hidekazu Tomimoto; Toshiro Okazaki; Yuichi Oike; Wen-Jie Song
Journal:  J Physiol       Date:  2012-05-28       Impact factor: 5.182

2.  Computational model of a circulation current that controls electrochemical properties in the mammalian cochlea.

Authors:  Fumiaki Nin; Hiroshi Hibino; Shingo Murakami; Toshihiro Suzuki; Yasuo Hisa; Yoshihisa Kurachi
Journal:  Proc Natl Acad Sci U S A       Date:  2012-05-22       Impact factor: 11.205

3.  The mechanism underlying maintenance of the endocochlear potential by the K+ transport system in fibrocytes of the inner ear.

Authors:  Naoko Adachi; Takamasa Yoshida; Fumiaki Nin; Genki Ogata; Soichiro Yamaguchi; Toshihiro Suzuki; Sizuo Komune; Yasuo Hisa; Hiroshi Hibino; Yoshihisa Kurachi
Journal:  J Physiol       Date:  2013-07-08       Impact factor: 5.182

4.  Precise toxigenic ablation of intermediate cells abolishes the "battery" of the cochlear duct.

Authors:  Hyo Jeong Kim; Michael Anne Gratton; Jeong-Han Lee; Maria Cristina Perez Flores; Wenying Wang; Karen J Doyle; Friedrich Beermann; Michael A Crognale; Ebenezer N Yamoah
Journal:  J Neurosci       Date:  2013-09-04       Impact factor: 6.167

Review 5.  Regulation of sodium transport in the inner ear.

Authors:  Sung Huhn Kim; Daniel C Marcus
Journal:  Hear Res       Date:  2011-05-18       Impact factor: 3.208

6.  Functional expression of P2X4 receptor in capillary endothelial cells of the cochlear spiral ligament and its role in regulating the capillary diameter.

Authors:  T Wu; M Dai; X R Shi; Z G Jiang; A L Nuttall
Journal:  Am J Physiol Heart Circ Physiol       Date:  2011-04-01       Impact factor: 4.733

Review 7.  Form and function of the mammalian inner ear.

Authors:  Eric G Ekdale
Journal:  J Anat       Date:  2015-04-25       Impact factor: 2.610

8.  Adaptation of Cochlear Amplification to Low Endocochlear Potential.

Authors:  Yi Wang; Elika Fallah; Elizabeth S Olson
Journal:  Biophys J       Date:  2019-03-30       Impact factor: 4.033

9.  Regulation of membrane KCNQ1/KCNE1 channel density by sphingomyelin synthase 1.

Authors:  Meikui Wu; Makoto Takemoto; Makoto Taniguchi; Toru Takumi; Toshiro Okazaki; Wen-Jie Song
Journal:  Am J Physiol Cell Physiol       Date:  2016-05-18       Impact factor: 4.249

10.  Cell-type-specific roles of Na+/K+ ATPase subunits in Drosophila auditory mechanosensation.

Authors:  Madhuparna Roy; Elena Sivan-Loukianova; Daniel F Eberl
Journal:  Proc Natl Acad Sci U S A       Date:  2012-12-17       Impact factor: 11.205

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.