Literature DB >> 12208541

Aquaporin-2 expression in the mammalian cochlea and investigation of its role in Meniere's disease.

Anand N Mhatre1, Jussi Jero, Ilaria Chiappini, Giulia Bolasco, Maurizio Barbara, Anil K Lalwani.   

Abstract

The expression pattern of aquaporin-2 (AQP2), a vasopressin regulated member of the aquaporin gene family, in the cochlea and its potential role in Meniere's disease was investigated. RT-PCR screen of multiple rat tissues identified AQP2 transcripts in the cochlea, testis and kidney and an absence of tissue-specific splice variants. The level of AQP2 transcript in the cochlea was 10-fold lower relative to its expression in the testis and kidney. Western blot analysis demonstrated a single, 29 kDa band in the membrane fractions from cochlea, testis and the kidney. In the rat and mouse cochlea, AQP2 was expressed in the structures bordering the endolymph, including Reissner's membrane, the organ of Corti, inner and outer sulcus cells and the spiral limbus. A mutation screen of AQP2 in 12 individuals with Meniere's disease did not identify any sequence alterations or mutations within the four coding exons of AQP2 and their intron-exon junctions. The physiological role of AQP2 in water transport and its expression pattern in the cochlea suggests an important role for AQP2 in fluid homeostasis of the inner ear; however, its role in the pathogenesis in Meniere's disease remains to be established.

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Year:  2002        PMID: 12208541     DOI: 10.1016/s0378-5955(02)00452-5

Source DB:  PubMed          Journal:  Hear Res        ISSN: 0378-5955            Impact factor:   3.208


  13 in total

Review 1.  Aquaporin-mediated fluid regulation in the inner ear.

Authors:  Eric Beitz; Hans-Peter Zenner; Joachim E Schultz
Journal:  Cell Mol Neurobiol       Date:  2003-06       Impact factor: 5.046

Review 2.  [Aquaporine. Discovery, function, and significance for otorhinolaryngology].

Authors:  H Löwenheim; B Hirt
Journal:  HNO       Date:  2004-08       Impact factor: 1.284

Review 3.  Genetic disorders of transporters/channels in the inner ear and their relation to the kidney.

Authors:  Theo A Peters; Leo A H Monnens; Cor W R J Cremers; Jo H A J Curfs
Journal:  Pediatr Nephrol       Date:  2004-09-09       Impact factor: 3.714

4.  Sequence variants in host cell factor C1 are associated with Ménière's disease.

Authors:  Jeffrey T Vrabec; Liqian Liu; Bingshan Li; Suzanne M Leal
Journal:  Otol Neurotol       Date:  2008-06       Impact factor: 2.311

5.  Quantitative Analysis of Aquaporin Expression Levels during the Development and Maturation of the Inner Ear.

Authors:  Takushi Miyoshi; Taro Yamaguchi; Kiyokazu Ogita; Yasuko Tanaka; Ken-Ichi Ishibashi; Hiroaki Ito; Taisuke Kobayashi; Takayuki Nakagawa; Juichi Ito; Koichi Omori; Norio Yamamoto
Journal:  J Assoc Res Otolaryngol       Date:  2016-12-21

6.  The Polymorphic Analysis of the Human Potassium Channel KCNE Gene Family in Meniere's Disease-A Preliminary Study.

Authors:  Qingqing Dai; Dan Wang; Hong Zheng
Journal:  J Int Adv Otol       Date:  2019-04       Impact factor: 1.017

7.  Molecular biology of hearing.

Authors:  Timo Stöver; Marc Diensthuber
Journal:  GMS Curr Top Otorhinolaryngol Head Neck Surg       Date:  2012-04-26

8.  Genetics of recurrent vertigo and vestibular disorders.

Authors:  Irene Gazquez; Jose A Lopez-Escamez
Journal:  Curr Genomics       Date:  2011-09       Impact factor: 2.236

Review 9.  Aquaporins in development -- a review.

Authors:  Huishu Liu; E Marelyn Wintour
Journal:  Reprod Biol Endocrinol       Date:  2005-05-11       Impact factor: 5.211

Review 10.  The genetics of Ménière's disease.

Authors:  Giuseppe Chiarella; C Petrolo; E Cassandro
Journal:  Appl Clin Genet       Date:  2015-01-08
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