| Literature DB >> 11435462 |
T Usui1, M Hara, H Satoh, N Moriyama, H Kagaya, S Amano, T Oshika, Y Ishii, N Ibaraki, C Hara, M Kunimi, E Noiri, K Tsukamoto, J Inatomi, H Kawakami, H Endou, T Igarashi, A Goto, T Fujita, M Araie, G Seki.
Abstract
Proximal renal tubular acidosis associated with ocular abnormalities such as band keratopathy, glaucoma, and cataracts is caused by mutations in the Na(+)-HCO(3)(-) cotransporter (NBC-1). However, the mechanism by which NBC-1 inactivation leads to such ocular abnormalities remains to be elucidated. By immunological analysis of human and rat eyes, we demonstrate that both kidney type (kNBC-1) and pancreatic type (pNBC-1) transporters are present in the corneal endothelium, trabecular meshwork, ciliary epithelium, and lens epithelium. In the human lens epithelial (HLE) cells, RT-PCR detected mRNAs of both kNBC-1 and pNBC-1. Although a Na(+)-HCO(3)-cotransport activity has not been detected in mammalian lens epithelia, cell pH (pH(i)) measurements revealed the presence of Cl(-)-independent, electrogenic Na(+)-HCO(3)-cotransport activity in HLE cells. In addition, up to 80% of amiloride-insensitive pH(i) recovery from acid load in the presence of HCO(3)(-)/CO(2) was inhibited by adenovirus-mediated transfer of a specific hammerhead ribozyme against NBC-1, consistent with a major role of NBC-1 in overall HCO(3)-transport by the lens epithelium. These results indicate that the normal transport activity of NBC-1 is indispensable not only for the maintenance of corneal and lenticular transparency but also for the regulation of aqueous humor outflow.Entities:
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Year: 2001 PMID: 11435462 PMCID: PMC209339 DOI: 10.1172/JCI11869
Source DB: PubMed Journal: J Clin Invest ISSN: 0021-9738 Impact factor: 14.808