Articles producció científica> Enginyeria Electrònica, Elèctrica i Automàtica

Dysfunctional LAT2 amino acid transporter is associated with cataract in mouse and humans

  • Dades identificatives

    Identificador: imarina:5764110
    Autors:
    Knopfel, Emilia BoiadjievaVilches, ClaraCamargo, Simone M RErrasti-Murugarren, EkaitzStaubli, AndrinaMayayo, ClaraMunier, Francis LMiroshnikova, NataliyaPoncet, NadegeJunza, AlexandraBhattacharya, Shomi SPrat, EstherBerry, VanitaBerger, WolfgangHeon, EliseMoore, Anthony TYanes, OscarNunes, VirginiaPalacin, ManuelVerrey, FrancoisKloeckener-Gruissem, Barbara
    Resum:
    © 2007 - 2019 Frontiers Media S.A. All Rights Reserved. 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.
  • Altres:

    Autor segons l'article: Knopfel, Emilia Boiadjieva; Vilches, Clara; Camargo, Simone M R; Errasti-Murugarren, Ekaitz; Staubli, Andrina; Mayayo, Clara; Munier, Francis L; Miroshnikova, Nataliya; Poncet, Nadege; Junza, Alexandra; Bhattacharya, Shomi S; Prat, Esther; Berry, Vanita; Berger, Wolfgang; Heon, Elise; Moore, Anthony T; Yanes, Oscar; Nunes, Virginia; Palacin, Manuel; Verrey, Francois; Kloeckener-Gruissem, Barbara
    Departament: Enginyeria Electrònica, Elèctrica i Automàtica
    Autor/s de la URV: Junza Martínez, Alexandra / Yanes Torrado, Óscar
    Paraules clau: Unclassified drug Tat1 protein Slc7a8 gene Senile cataract Risk factor Patient screen Ocular tissues Nonhuman Mouse model Mouse Male Major clinical study Lens epithelium Lat2 protein Human cell Human Gene mutation Gene expression Gene Female Essential amino acid Disease association Controlled study Congenital cataract Ciliary body epithelium Cataract Article Animal tissue Animal model Animal experiment Amino acid transporters lat2 and tat1 Amino acid transporter Amino acid transport ocular tissues mouse model gene expression cataract amino acid transporters lat2 and tat1
    Resum: © 2007 - 2019 Frontiers Media S.A. All Rights Reserved. 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.
    Àrees temàtiques: Zootecnia / recursos pesqueiros Saúde coletiva Química Psicología Physiology (medical) Physiology Odontología Nutrição Medicina veterinaria Medicina iii Medicina ii Medicina i Interdisciplinar Farmacia Ensino Engenharias iv Educação física Ciências biológicas iii Ciências biológicas ii Ciências biológicas i Ciências ambientais Ciências agrárias i Ciência de alimentos Biotecnología Astronomia / física Administração pública e de empresas, ciências contábeis e turismo
    Accès a la llicència d'ús: https://creativecommons.org/licenses/by/3.0/es/
    ISSN: 1664042X
    Adreça de correu electrònic de l'autor: oscar.yanes@urv.cat alexandra.junza@urv.cat
    Identificador de l'autor: 0000-0003-3695-7157 0000-0001-7205-0419
    Data d'alta del registre: 2024-10-12
    Versió de l'article dipositat: info:eu-repo/semantics/publishedVersion
    Enllaç font original: https://www.frontiersin.org/articles/10.3389/fphys.2019.00688/full
    URL Document de llicència: https://repositori.urv.cat/ca/proteccio-de-dades/
    Referència a l'article segons font original: Frontiers In Physiology. 10 (JUN): 688-
    Referència de l'ítem segons les normes APA: Knopfel, Emilia Boiadjieva; Vilches, Clara; Camargo, Simone M R; Errasti-Murugarren, Ekaitz; Staubli, Andrina; Mayayo, Clara; Munier, Francis L; Miros (2019). Dysfunctional LAT2 amino acid transporter is associated with cataract in mouse and humans. Frontiers In Physiology, 10(JUN), 688-. DOI: 10.3389/fphys.2019.00688
    DOI de l'article: 10.3389/fphys.2019.00688
    Entitat: Universitat Rovira i Virgili
    Any de publicació de la revista: 2019
    Tipus de publicació: Journal Publications
  • Paraules clau:

    Physiology,Physiology (Medical)
    Unclassified drug
    Tat1 protein
    Slc7a8 gene
    Senile cataract
    Risk factor
    Patient screen
    Ocular tissues
    Nonhuman
    Mouse model
    Mouse
    Male
    Major clinical study
    Lens epithelium
    Lat2 protein
    Human cell
    Human
    Gene mutation
    Gene expression
    Gene
    Female
    Essential amino acid
    Disease association
    Controlled study
    Congenital cataract
    Ciliary body epithelium
    Cataract
    Article
    Animal tissue
    Animal model
    Animal experiment
    Amino acid transporters lat2 and tat1
    Amino acid transporter
    Amino acid transport
    ocular tissues
    mouse model
    gene expression
    cataract
    amino acid transporters lat2 and tat1
    Zootecnia / recursos pesqueiros
    Saúde coletiva
    Química
    Psicología
    Physiology (medical)
    Physiology
    Odontología
    Nutrição
    Medicina veterinaria
    Medicina iii
    Medicina ii
    Medicina i
    Interdisciplinar
    Farmacia
    Ensino
    Engenharias iv
    Educação física
    Ciências biológicas iii
    Ciências biológicas ii
    Ciências biológicas i
    Ciências ambientais
    Ciências agrárias i
    Ciência de alimentos
    Biotecnología
    Astronomia / física
    Administração pública e de empresas, ciências contábeis e turismo
  • Documents:

  • Cerca a google

    Search to google scholar