Evidence map›Paper›PMID 25761365›Full record

ArticleFASEB journal : official publication of the Federation of American Societies for Experimental Biology2015

Integration of computational modeling with membrane transport studies reveals new insights into amino acid exchange transport mechanisms.

Kate L Widdows, Nuttanont Panitchob, Ian P Crocker, Colin P Please, Mark A Hanson, Colin P Sibley, Edward D Johnstone, Bram G Sengers, Rohan M Lewis, Jocelyn D Glazier

Abstract read
In one paragraph

Article in FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

14 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Homocysteine Metabolism in Pregnancy and Developmental Impacts.Frontiers in cell and developmental biology · 2022
    Review
  5. Article
  6. Review
  7. Article
  8. Blood flow and transport in the human placenta.Annual review of fluid mechanics · 2019
    Article
  9. Review
  10. Article
  11. Treating the dysfunctional placenta.The Journal of endocrinology · 2017
    Review
  12. Article
  13. Phenylalanine transfer across the isolated perfused human placenta: an experimental and modeling investigation.American journal of physiology. Regulatory, integrative and comparative physiology · 2016
    Article
  14. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Kate L Widdows*Maternal and Fetal Health Research Centre, Institute of Human Development, University of Manchester, Manchester, United Kingdom; St. Mary's Hospital and Central Manchester University Hospitals National Health Service Foundation Trust, Manchester Academic Health Science Centre, Manchester, United Kingdom; Bioengineering Science Research Group, Faculty of Engineering and the Environment, University of Southampton, Southampton, United Kingdom; Mathematical Institute, Oxford University, Oxford, United Kingdom; and Faculty of Medicine, and Institute for Life Sciences, University of Southampton, Southampton, United Kingdom.
Nuttanont Panitchob*Maternal and Fetal Health Research Centre, Institute of Human Development, University of Manchester, Manchester, United Kingdom; St. Mary's Hospital and Central Manchester University Hospitals National Health Service Foundation Trust, Manchester Academic Health Science Centre, Manchester, United Kingdom; Bioengineering Science Research Group, Faculty of Engineering and the Environment, University of Southampton, Southampton, United Kingdom; Mathematical Institute, Oxford University, Oxford, United Kingdom; and Faculty of Medicine, and Institute for Life Sciences, University of Southampton, Southampton, United Kingdom.
Ian P Crocker*Maternal and Fetal Health Research Centre, Institute of Human Development, University of Manchester, Manchester, United Kingdom; St. Mary's Hospital and Central Manchester University Hospitals National Health Service Foundation Trust, Manchester Academic Health Science Centre, Manchester, United Kingdom; Bioengineering Science Research Group, Faculty of Engineering and the Environment, University of Southampton, Southampton, United Kingdom; Mathematical Institute, Oxford University, Oxford, United Kingdom; and Faculty of Medicine, and Institute for Life Sciences, University of Southampton, Southampton, United Kingdom.
Colin P Please*Maternal and Fetal Health Research Centre, Institute of Human Development, University of Manchester, Manchester, United Kingdom; St. Mary's Hospital and Central Manchester University Hospitals National Health Service Foundation Trust, Manchester Academic Health Science Centre, Manchester, United Kingdom; Bioengineering Science Research Group, Faculty of Engineering and the Environment, University of Southampton, Southampton, United Kingdom; Mathematical Institute, Oxford University, Oxford, United Kingdom; and Faculty of Medicine, and Institute for Life Sciences, University of Southampton, Southampton, United Kingdom.
Mark A Hanson*Maternal and Fetal Health Research Centre, Institute of Human Development, University of Manchester, Manchester, United Kingdom; St. Mary's Hospital and Central Manchester University Hospitals National Health Service Foundation Trust, Manchester Academic Health Science Centre, Manchester, United Kingdom; Bioengineering Science Research Group, Faculty of Engineering and the Environment, University of Southampton, Southampton, United Kingdom; Mathematical Institute, Oxford University, Oxford, United Kingdom; and Faculty of Medicine, and Institute for Life Sciences, University of Southampton, Southampton, United Kingdom.
Colin P Sibley*Maternal and Fetal Health Research Centre, Institute of Human Development, University of Manchester, Manchester, United Kingdom; St. Mary's Hospital and Central Manchester University Hospitals National Health Service Foundation Trust, Manchester Academic Health Science Centre, Manchester, United Kingdom; Bioengineering Science Research Group, Faculty of Engineering and the Environment, University of Southampton, Southampton, United Kingdom; Mathematical Institute, Oxford University, Oxford, United Kingdom; and Faculty of Medicine, and Institute for Life Sciences, University of Southampton, Southampton, United Kingdom.
Edward D Johnstone*Maternal and Fetal Health Research Centre, Institute of Human Development, University of Manchester, Manchester, United Kingdom; St. Mary's Hospital and Central Manchester University Hospitals National Health Service Foundation Trust, Manchester Academic Health Science Centre, Manchester, United Kingdom; Bioengineering Science Research Group, Faculty of Engineering and the Environment, University of Southampton, Southampton, United Kingdom; Mathematical Institute, Oxford University, Oxford, United Kingdom; and Faculty of Medicine, and Institute for Life Sciences, University of Southampton, Southampton, United Kingdom.
Bram G Sengers*Maternal and Fetal Health Research Centre, Institute of Human Development, University of Manchester, Manchester, United Kingdom; St. Mary's Hospital and Central Manchester University Hospitals National Health Service Foundation Trust, Manchester Academic Health Science Centre, Manchester, United Kingdom; Bioengineering Science Research Group, Faculty of Engineering and the Environment, University of Southampton, Southampton, United Kingdom; Mathematical Institute, Oxford University, Oxford, United Kingdom; and Faculty of Medicine, and Institute for Life Sciences, University of Southampton, Southampton, United Kingdom.
Rohan M Lewis*Maternal and Fetal Health Research Centre, Institute of Human Development, University of Manchester, Manchester, United Kingdom; St. Mary's Hospital and Central Manchester University Hospitals National Health Service Foundation Trust, Manchester Academic Health Science Centre, Manchester, United Kingdom; Bioengineering Science Research Group, Faculty of Engineering and the Environment, University of Southampton, Southampton, United Kingdom; Mathematical Institute, Oxford University, Oxford, United Kingdom; and Faculty of Medicine, and Institute for Life Sciences, University of Southampton, Southampton, United Kingdom rohan.lewis@soton.ac.uk.
Jocelyn D Glazier*Maternal and Fetal Health Research Centre, Institute of Human Development, University of Manchester, Manchester, United Kingdom; St. Mary's Hospital and Central Manchester University Hospitals National Health Service Foundation Trust, Manchester Academic Health Science Centre, Manchester, United Kingdom; Bioengineering Science Research Group, Faculty of Engineering and the Environment, University of Southampton, Southampton, United Kingdom; Mathematical Institute, Oxford University, Oxford, United Kingdom; and Faculty of Medicine, and Institute for Life Sciences, University of Southampton, Southampton, United Kingdom.

Funding

Biotechnology and Biological Sciences Research Council BB/I011250/1Biotechnology and Biological Sciences Research Council BB/I011315/1British Heart Foundation
6 · The paper itself

Abstract

Uptake of system L amino acid substrates into isolated placental plasma membrane vesicles in the absence of opposing side amino acid (zero-trans uptake) is incompatible with the concept of obligatory exchange, where influx of amino acid is coupled to efflux. We therefore hypothesized that system L amino acid exchange transporters are not fully obligatory and/or that amino acids are initially present inside the vesicles. To address this, we combined computational modeling with vesicle transport assays and transporter localization studies to investigate the mechanisms mediating [(14)C]L-serine (a system L substrate) transport into human placental microvillous plasma membrane (MVM) vesicles. The carrier model provided a quantitative framework to test the 2 hypotheses that l-serine transport occurs by either obligate exchange or nonobligate exchange coupled with facilitated transport (mixed transport model). The computational model could only account for experimental [(14)C]L-serine uptake data when the transporter was not exclusively in exchange mode, best described by the mixed transport model. MVM vesicle isolates contained endogenous amino acids allowing for potential contribution to zero-trans uptake. Both L-type amino acid transporter (LAT)1 and LAT2 subtypes of system L were distributed to MVM, with L-serine transport attributed to LAT2. These findings suggest that exchange transporters do not function exclusively as obligate exchangers.

Indexed as

Computer SimulationModels, BiologicalAmino AcidsAmino Acid Transport System y+Biological TransportBlotting, WesternCarbon RadioisotopesCell MembraneFemaleFluorescent Antibody TechniqueFusion Regulatory Protein 1, Light ChainsHumansLarge Neutral Amino Acid-Transporter 1MicrovilliPlacentaPregnancyAmino AcidsAmino Acid Transport System y+Carbon RadioisotopesFusion Regulatory Protein 1, Light ChainsLarge Neutral Amino Acid-Transporter 1SerineSLC7A8 protein, humanantiportersfacilitated transportLAT2 (SLC7A8)overshoot phenomena

Identifiers

PMID25761365
PMCPMC4469330

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.