Evidence map›Paper›PMID 19564394›Full record

ArticleThe Journal of physiology2009

Homocysteine transport by systems L, A and y+L across the microvillous plasma membrane of human placenta.

Eleni Tsitsiou, Colin P Sibley, Stephen W D'Souza, Otilia Catanescu, Donald W Jacobsen, Jocelyn D Glazier

Open access · greenAbstract read
In one paragraph

Article in The Journal of physiology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.9field-weighted citation impact, top 15% of its field
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

19 citing papers in PubMed, 39 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Homocysteine Metabolism in Pregnancy and Developmental Impacts.Frontiers in cell and developmental biology · 2022
    Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. Integration of computational modeling with membrane transport studies reveals new insights into amino acid exchange transport mechanisms.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2015
    Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Methionine, homocysteine, one carbon metabolism and fetal growth.Reviews in endocrine & metabolic disorders · 2012
    Review
  16. Review
  17. Review
  18. Article
  19. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 4 institutions in 2 countries.

Eleni TsitsiouMaternal and Fetal Health Research Group, University of Manchester, St Mary's Hospital, Hathersage Road, Manchester M13 0JH, UK.
Colin P Sibley
Stephen W D'Souza
Otilia Catanescu
Donald W Jacobsen
Jocelyn D Glazier
St Mary's Hospital · GBCase Western Reserve University · USCleveland Clinic Lerner College of Medicine · USManchester Academic Health Science Centre · GB

Funding

Homocysteine: Vascular Biochemistry and MetabolismR37HL052234 · NHLBI · CLEVELAND CLINIC LERNER COM-CWRU · PI JACOBSEN, DONALD WELDON · 2006 to 2010
$1.9M
HOMOCYSTEINE--VASCULAR BIOCHEMISTRY AND METABOLISMR01HL052234 · NHLBI · CLEVELAND CLINIC LERNER COL/MED-CWRU · PI JACOBSEN, DONALD WELDON · 1995 to 2005
$1.8M
Medical Research Council G0500647NHLBI NIH HHS HL52234NHLBI NIH HHS R01 HL052234NHLBI NIH HHS R37 HL052234
6 · The paper itself

Abstract

Elevated maternal plasma levels of homocysteine (Hcy) are associated with pregnancy complications and adverse neonatal outcomes, suggesting placental transport of Hcy may impact on fetal development. However, such transport mechanisms have not been defined. In this study we characterise Hcy transport mechanisms across the microvillous plasma membrane (MVM) of the syncytiotrophoblast, the transporting epithelium of human placenta. Three candidate transport systems, systems L, A and y(+)L, were examined utilising competitive inhibition to investigate the effects of Hcy on the uptake of well-characterised radiolabelled substrates for each system into isolated MVM vesicles, and that of model substrates on 10 microm [(35)S]l-Hcy uptake. System L activity was inhibited by both l-Hcy and dl-Hcy, comparable to model substrates including 2-aminobicyclo[2.2.1]heptane-2-carboxylic acid (BCH). System L constituted the major transport mechanism, with significant BCH inhibition (69%) of [(35)S]l-Hcy uptake. System A activity was also inhibited by l-Hcy and dl-Hcy with a smaller contribution (21%) to [(35)S]l-Hcy uptake. Inhibition by l-Hcy and dl-Hcy of system y(+)L activity was Na(+) sensitive with a significant inhibition constant (K(i)) shift observed following K(+) replacement; l-arginine reduced [(35)S]l-Hcy uptake by 19%. Kinetic modelling of [(35)S]l-Hcy uptake resolved two, Na(+)-independent, transport components (K(m) 72 microm and 9.7 mm). This study provides evidence for the involvement of systems L, A and y(+)L in placental Hcy transport. Such transport, by competing with endogenous amino acids for transporter activity, could have major implications for syncytiotrophoblast metabolism and function as well as fetal development.

Indexed as

Amino Acid Transport System AAmino Acid Transport System y+Amino Acid Transport System y+LBiological Transport, ActiveCell MembraneFemaleHomocysteineHumansIn Vitro TechniquesMicrovilliPlacentaAmino Acid Transport System AAmino Acid Transport System y+Amino Acid Transport System y+LHomocysteine

Identifiers

PMID19564394
PMCPMC2756434
OpenAlexW2154691274

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.