Evidence map›Paper›PMID 22028793›Full record

ArticlePloS one2011

The expression and function of fatty acid transport protein-2 and -4 in the murine placenta.

Takuya Mishima, Jeffrey H Miner, Mayumi Morizane, Andreas Stahl, Yoel Sadovsky

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

32 citing papers in PubMed, 67 citations in OpenAlex.

  1. Review
  2. The role of candidate transport proteins in β-cell long-chain fatty acid uptake: Where are we now?Diabetic medicine : a journal of the British Diabetic Association · 2023
    Review
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  12. Fatty acid transporting proteins: Roles in brain development, aging, and stroke.Prostaglandins, leukotrienes, and essential fatty acids · 2018
    Review
  13. Article
  14. [Expression of FABP7 in mouse placenta tissue and human trophoblast HTR-8/Svneo cells].Nan fang yi ke da xue xue bao = Journal of Southern Medical University · 2017
    Article
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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

5 authors at 4 institutions in 1 country.

Takuya MishimaDepartment of Obstetrics, Gynecology and Reproductive Sciences, Magee-Womens Research Institute, University of Pittsburgh, Pittsburgh, Pennsylvania, United States of America.
Jeffrey H Miner
Mayumi Morizane
Andreas Stahl
Yoel Sadovsky
Magee-Womens Research Institute · USUniversity of California, Berkeley · USUniversity of Pittsburgh · USWashington University in St. Louis · US

Funding

Regulation of Trophoblast Differentiation and FunctionR01ES011597 · NIEHS · WASHINGTON UNIVERSITY · PI SADOVSKY, YOEL · 2001 to 2011
$3.1M
Role of FATP4 in Skin DevelopmentR01AR049269 · NIAMS · WASHINGTON UNIVERSITY · PI MINER, JEFFREY H · 2003 to 2012
$2.4M
NIAMS NIH HHS R01 AR049269NIAMS NIH HHS R01AR049269NIEHS NIH HHS R01 ES011597NIEHS NIH HHS R01ES011597
6 · The paper itself

Abstract

backgroundThe uptake and trans-placental trafficking of fatty acids from the maternal blood into the fetal circulation are essential for embryonic development, and involve several families of proteins. Fatty acid transport proteins (FATPs) uniquely transport fatty acids into cells. We surmised that placental FATPs are germane for fetal growth, and are regulated during hypoxic stress, which is associated with reduced fat supply to the fetus. METHODOLOGY/PRINCIPAL

findingsUsing cultured primary term human trophoblasts we found that FATP2, FATP4 and FATP6 were highly expressed in trophoblasts. Hypoxia enhanced the expression of trophoblastic FATP2 and reduced the expression of FATP4, with no change in FATP6. We also found that Fatp2 and Fatp4 are expressed in the mouse amnion and placenta, respectively. Mice deficient in Fatp2 or Fatp4 did not deviate from normal Mendelian distribution, with both embryos and placentas exhibiting normal weight and morphology, triglyceride content, and expression of genes related to fatty acid mobilization. CONCLUSIONS/SIGNIFICANCE: We conclude that even though hypoxia regulates the expression of FATP2 and FATP4 in human trophoblasts, mouse Fatp2 and Fatp4 are not essential for intrauterine fetal growth.

Indexed as

Gene Expression RegulationAnimalsCell HypoxiaCoenzyme A LigasesFatty Acid Transport ProteinsFemaleHumansMiceMutationPlacentaPregnancyTrophoblastsCoenzyme A LigasesFATP2 protein, mouseFatty Acid Transport ProteinsSlc27a4 protein, mouse

Identifiers

PMID22028793
PMCPMC3197585
OpenAlexW2133849172

What OpenQuestion holds

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LicenceCC BY
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.