Dysfunctional LAT2 Amino Acid Transporter Is Associated With Cataract in Mouse and Humans.

Détails

ID Serval
serval:BIB_33A831DC88A0
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Titre
Dysfunctional LAT2 Amino Acid Transporter Is Associated With Cataract in Mouse and Humans.
Périodique
Frontiers in physiology
Auteur(s)
Knöpfel E.B., Vilches C., Camargo SMR, Errasti-Murugarren E., Stäubli A., Mayayo C., Munier F.L., Miroshnikova N., Poncet N., Junza A., Bhattacharya S.S., Prat E., Berry V., Berger W., Heon E., Moore A.T., Yanes Ó., Nunes V., Palacín M., Verrey F., Kloeckener-Gruissem B.
ISSN
1664-042X (Print)
ISSN-L
1664-042X
Statut éditorial
Publié
Date de publication
2019
Peer-reviewed
Oui
Volume
10
Pages
688
Langue
anglais
Notes
Publication types: Journal Article
Publication Status: epublish
Résumé
Cataract, the loss of ocular lens transparency, accounts for ∼50% of worldwide blindness and has been associated with water and solute transport dysfunction across lens cellular barriers. We show that neutral amino acid antiporter LAT2 (Slc7a8) and uniporter TAT1 (Slc16a10) are expressed on mouse ciliary epithelium and LAT2 also in lens epithelium. Correspondingly, deletion of LAT2 induced a dramatic decrease in lens essential amino acid levels that was modulated by TAT1 defect. Interestingly, the absence of LAT2 led to increased incidence of cataract in mice, in particular in older females, and a synergistic effect was observed with simultaneous lack of TAT1. Screening SLC7A8 in patients diagnosed with congenital or age-related cataract yielded one homozygous single nucleotide deletion segregating in a family with congenital cataract. Expressed in HeLa cells, this LAT2 mutation did not support amino acid uptake. Heterozygous LAT2 variants were also found in patients with cataract some of which showed a reduced transport function when expressed in HeLa cells. Whether heterozygous LAT2 variants may contribute to the pathology of cataract needs to be further investigated. Overall, our results suggest that defects of amino acid transporter LAT2 are implicated in cataract formation, a situation that may be aggravated by TAT1 defects.
Mots-clé
amino acid transporters LAT2 and TAT1, cataract, gene expression, mouse model, ocular tissues, patient screen
Pubmed
Web of science
Open Access
Oui
Création de la notice
01/07/2019 16:14
Dernière modification de la notice
20/08/2019 13:19
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