December 2002
Volume 43, Issue 13
Free
ARVO Annual Meeting Abstract  |   December 2002
Functional and Molecular Characterization of Taurine Transporter, TAUT, at the Inner Blood-retinal Barrier
Author Affiliations & Notes
  • K Hosoya
    Dept Pharmaceutical Sci Toayama Med & Pharm Univ Toyama Japan
  • I Isobe
    Dept Pharmaceutical Sci Toayama Med & Pharm Univ Toyama Japan
  • YS Kang
    New Industry Creation Hatchery Center
    Tohoku Univ Sendai Japan
  • S Ohtsuki
    Graduate School of Pharmaceutical Sciences
    Tohoku Univ Sendai Japan
  • T Terasaki
    New Industry Creation Hatchery Center
    Tohoku Univ Sendai Japan
  • M TomiCREST of Japan Science and Technology Corporation
    Dept Pharmaceutical Sci Toayama Med & Pharm Univ Toyama Japan
  • Footnotes
    Commercial Relationships   K. Hosoya, None; I. Isobe, None; Y.S. Kang, None; S. Ohtsuki, None; T. Terasaki, None; M. Tomi, None. Grant Identification: Support: Grant-in-Aid from the Ministry of Education, Science, Sports, and Culture, Japan
Investigative Ophthalmology & Visual Science December 2002, Vol.43, 3262. doi:
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      K Hosoya, I Isobe, YS Kang, S Ohtsuki, T Terasaki, M TomiCREST of Japan Science and Technology Corporation; Functional and Molecular Characterization of Taurine Transporter, TAUT, at the Inner Blood-retinal Barrier . Invest. Ophthalmol. Vis. Sci. 2002;43(13):3262.

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      © ARVO (1962-2015); The Authors (2016-present)

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Abstract

Abstract: : Purpose: Taurine, the most abundant amino acid in the retina, may play a role in osmoregulating and modulating antioxidant. The purpose of this study was to characterize taurine transport and regulation of taurine transporter (TAUT) at the inner blood-retinal barrier (iBRB). Methods: The conditionally immortalized retinal capillary endothelial cell line (TR-iBRB) was used as an in vitro model for the iBRB. TR-iBRB cells were cultured at 33C and [3H]taurine uptake was measured at 37C. The quantitative real-time PCR was performed to determine the mRNA level in the cells. Results: RT-PCR and Western blot analysis indicated that TAUT is expressed in TR-iBRB cells. [3H]Taurine uptake by TR-iBRB cells was a temperature-, Na+-, and Cl- -dependent manner. It was concentration-dependent with a Km of 22.2 µM and inhibited by ß-alanine, hypotaurine, and taurocyamine. The quantitative real-time PCR revealed an increase of TAUT under the hypertonic conditions. Conclusion: TAUT mediates taurine transport at the iBRB and is regulated under pathological conditions.

Keywords: 595 taurine • 556 retina: neurochemistry • 446 ion transporters 
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