---
_id: '1183'
abstract:
- lang: eng
  text: Autism spectrum disorders (ASD) are a group of genetic disorders often overlapping
    with other neurological conditions. We previously described abnormalities in the
    branched-chain amino acid (BCAA) catabolic pathway as a cause of ASD. Here, we
    show that the solute carrier transporter 7a5 (SLC7A5), a large neutral amino acid
    transporter localized at the blood brain barrier (BBB), has an essential role
    in maintaining normal levels of brain BCAAs. In mice, deletion of Slc7a5 from
    the endothelial cells of the BBB leads to atypical brain amino acid profile, abnormal
    mRNA translation, and severe neurological abnormalities. Furthermore, we identified
    several patients with autistic traits and motor delay carrying deleterious homozygous
    mutations in the SLC7A5 gene. Finally, we demonstrate that BCAA intracerebroventricular
    administration ameliorates abnormal behaviors in adult mutant mice. Our data elucidate
    a neurological syndrome defined by SLC7A5 mutations and support an essential role
    for the BCAA in human brain function.
acknowledgement: "This work was supported by NICHD (P01HD070494) and SFARI (grant
  275275) to J.G.G., and FWF (SFB35_3523) to G.N.\r\nWe thank A.C. Manzano, Mike Liu,
  and F. Marr for technical assistance, and R. Shigemoto and the IST Austria Electron
  Microscopy (EM) Facility for assistance. We acknowledge support from CIDR for genome-wide
  SNP analysis (X01HG008823) and Broad Institute Center for Mendelian Disorders (UM1HG008900
  to D. MacArthur), the Yale Center for Mendelian Disorders (U54HG006504 to M.G.),
  the Gregory M. Kiez and Mehmet Kutman Foundation (M.G.), Italian Ministry of Instruction
  University and Research (PON01_00937 to C.I.), and NIH (R01-GM108911 to A.S.). This
  work was supported by NICHD (P01HD070494) and SFARI (grant 275275) to J.G.G., and
  FWF (SFB35_3523) to G.N.\r\n\r\n#EMFacility"
article_processing_charge: No
article_type: original
author:
- first_name: Dora-Clara
  full_name: Tarlungeanu, Dora-Clara
  id: 2ABCE612-F248-11E8-B48F-1D18A9856A87
  last_name: Tarlungeanu
- first_name: Elena
  full_name: Deliu, Elena
  id: 37A40D7E-F248-11E8-B48F-1D18A9856A87
  last_name: Deliu
  orcid: 0000-0002-7370-5293
- first_name: Christoph
  full_name: Dotter, Christoph
  id: 4C66542E-F248-11E8-B48F-1D18A9856A87
  last_name: Dotter
  orcid: 0000-0002-9033-9096
- first_name: Majdi
  full_name: Kara, Majdi
  last_name: Kara
- first_name: Philipp
  full_name: Janiesch, Philipp
  last_name: Janiesch
- first_name: Mariafrancesca
  full_name: Scalise, Mariafrancesca
  last_name: Scalise
- first_name: Michele
  full_name: Galluccio, Michele
  last_name: Galluccio
- first_name: Mateja
  full_name: Tesulov, Mateja
  last_name: Tesulov
- first_name: Emanuela
  full_name: Morelli, Emanuela
  id: 3F4D1282-F248-11E8-B48F-1D18A9856A87
  last_name: Morelli
- first_name: Fatma
  full_name: Sönmez, Fatma
  last_name: Sönmez
- first_name: Kaya
  full_name: Bilgüvar, Kaya
  last_name: Bilgüvar
- first_name: Ryuichi
  full_name: Ohgaki, Ryuichi
  last_name: Ohgaki
- first_name: Yoshikatsu
  full_name: Kanai, Yoshikatsu
  last_name: Kanai
- first_name: Anide
  full_name: Johansen, Anide
  last_name: Johansen
- first_name: Seham
  full_name: Esharif, Seham
  last_name: Esharif
- first_name: Tawfeg
  full_name: Ben Omran, Tawfeg
  last_name: Ben Omran
- first_name: Meral
  full_name: Topcu, Meral
  last_name: Topcu
- first_name: Avner
  full_name: Schlessinger, Avner
  last_name: Schlessinger
- first_name: Cesare
  full_name: Indiveri, Cesare
  last_name: Indiveri
- first_name: Kent
  full_name: Duncan, Kent
  last_name: Duncan
- first_name: Ahmet
  full_name: Caglayan, Ahmet
  last_name: Caglayan
- first_name: Murat
  full_name: Günel, Murat
  last_name: Günel
- first_name: Joseph
  full_name: Gleeson, Joseph
  last_name: Gleeson
- first_name: Gaia
  full_name: Novarino, Gaia
  id: 3E57A680-F248-11E8-B48F-1D18A9856A87
  last_name: Novarino
  orcid: 0000-0002-7673-7178
citation:
  ama: Tarlungeanu D-C, Deliu E, Dotter C, et al. Impaired amino acid transport at
    the blood brain barrier is a cause of autism spectrum disorder. <i>Cell</i>. 2016;167(6):1481-1494.
    doi:<a href="https://doi.org/10.1016/j.cell.2016.11.013">10.1016/j.cell.2016.11.013</a>
  apa: Tarlungeanu, D.-C., Deliu, E., Dotter, C., Kara, M., Janiesch, P., Scalise,
    M., … Novarino, G. (2016). Impaired amino acid transport at the blood brain barrier
    is a cause of autism spectrum disorder. <i>Cell</i>. Cell Press. <a href="https://doi.org/10.1016/j.cell.2016.11.013">https://doi.org/10.1016/j.cell.2016.11.013</a>
  chicago: Tarlungeanu, Dora-Clara, Elena Deliu, Christoph Dotter, Majdi Kara, Philipp
    Janiesch, Mariafrancesca Scalise, Michele Galluccio, et al. “Impaired Amino Acid
    Transport at the Blood Brain Barrier Is a Cause of Autism Spectrum Disorder.”
    <i>Cell</i>. Cell Press, 2016. <a href="https://doi.org/10.1016/j.cell.2016.11.013">https://doi.org/10.1016/j.cell.2016.11.013</a>.
  ieee: D.-C. Tarlungeanu <i>et al.</i>, “Impaired amino acid transport at the blood
    brain barrier is a cause of autism spectrum disorder,” <i>Cell</i>, vol. 167,
    no. 6. Cell Press, pp. 1481–1494, 2016.
  ista: Tarlungeanu D-C, Deliu E, Dotter C, Kara M, Janiesch P, Scalise M, Galluccio
    M, Tesulov M, Morelli E, Sönmez F, Bilgüvar K, Ohgaki R, Kanai Y, Johansen A,
    Esharif S, Ben Omran T, Topcu M, Schlessinger A, Indiveri C, Duncan K, Caglayan
    A, Günel M, Gleeson J, Novarino G. 2016. Impaired amino acid transport at the
    blood brain barrier is a cause of autism spectrum disorder. Cell. 167(6), 1481–1494.
  mla: Tarlungeanu, Dora-Clara, et al. “Impaired Amino Acid Transport at the Blood
    Brain Barrier Is a Cause of Autism Spectrum Disorder.” <i>Cell</i>, vol. 167,
    no. 6, Cell Press, 2016, pp. 1481–94, doi:<a href="https://doi.org/10.1016/j.cell.2016.11.013">10.1016/j.cell.2016.11.013</a>.
  short: D.-C. Tarlungeanu, E. Deliu, C. Dotter, M. Kara, P. Janiesch, M. Scalise,
    M. Galluccio, M. Tesulov, E. Morelli, F. Sönmez, K. Bilgüvar, R. Ohgaki, Y. Kanai,
    A. Johansen, S. Esharif, T. Ben Omran, M. Topcu, A. Schlessinger, C. Indiveri,
    K. Duncan, A. Caglayan, M. Günel, J. Gleeson, G. Novarino, Cell 167 (2016) 1481–1494.
date_created: 2018-12-11T11:50:35Z
date_published: 2016-12-01T00:00:00Z
date_updated: 2024-03-25T23:30:07Z
day: '01'
ddc:
- '576'
- '616'
department:
- _id: GaNo
doi: 10.1016/j.cell.2016.11.013
file:
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  creator: system
  date_created: 2018-12-12T10:13:44Z
  date_updated: 2020-07-14T12:44:37Z
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  file_name: IST-2017-771-v1+1_Tarlungeanu_et_al._Final_edited.pdf
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file_date_updated: 2020-07-14T12:44:37Z
has_accepted_license: '1'
intvolume: '       167'
issue: '6'
language:
- iso: eng
month: '12'
oa: 1
oa_version: Submitted Version
page: 1481 - 1494
project:
- _id: 25473368-B435-11E9-9278-68D0E5697425
  call_identifier: FWF
  grant_number: F03523
  name: Transmembrane Transporters in Health and Disease
publication: Cell
publication_status: published
publisher: Cell Press
publist_id: '6170'
pubrep_id: '771'
quality_controlled: '1'
related_material:
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  - id: '395'
    relation: dissertation_contains
    status: public
scopus_import: '1'
status: public
title: Impaired amino acid transport at the blood brain barrier is a cause of autism
  spectrum disorder
type: journal_article
user_id: 8b945eb4-e2f2-11eb-945a-df72226e66a9
volume: 167
year: '2016'
...
