Evidence map›Paper›PMID 28320871›Full record

ArticleMolecular and cellular biology2017

Essential Roles of L-Type Amino Acid Transporter 1 in Syncytiotrophoblast Development by Presenting Fusogenic 4F2hc.

Ryuichi Ohgaki, Takahiro Ohmori, Saori Hara, Saya Nakagomi, Masami Kanai-Azuma, Kazuko Kaneda-Nakashima, Suguru Okuda, Shushi Nagamori, Yoshikatsu Kanai

Open access · bronzeAbstract read
In one paragraph

Article in Molecular and cellular biology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
3.9field-weighted citation impact, top 7% 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

39 citing papers in PubMed, 61 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Review
  18. Review
  19. Article
  20. 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

9 authors at 2 institutions in 1 country.

Ryuichi OhgakiDepartment of Bio-system Pharmacology, Graduate School of Medicine, Osaka University, Suita, Osaka, Japan.
Takahiro OhmoriDepartment of Bio-system Pharmacology, Graduate School of Medicine, Osaka University, Suita, Osaka, Japan.
Saori HaraDepartment of Bio-system Pharmacology, Graduate School of Medicine, Osaka University, Suita, Osaka, Japan.
Saya NakagomiDepartment of Bio-system Pharmacology, Graduate School of Medicine, Osaka University, Suita, Osaka, Japan.
Masami Kanai-AzumaCenter of Experimental Animals, Tokyo Medical and Dental University, Tokyo, Japan.
Kazuko Kaneda-NakashimaDepartment of Bio-system Pharmacology, Graduate School of Medicine, Osaka University, Suita, Osaka, Japan.
Suguru OkudaDepartment of Bio-system Pharmacology, Graduate School of Medicine, Osaka University, Suita, Osaka, Japan.
Shushi NagamoriDepartment of Bio-system Pharmacology, Graduate School of Medicine, Osaka University, Suita, Osaka, Japan.
Yoshikatsu KanaiDepartment of Bio-system Pharmacology, Graduate School of Medicine, Osaka University, Suita, Osaka, Japan ykanai@pharma1.med.osaka-u.ac.jp.
Osaka University · JPTokyo Medical and Dental University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The layers of the epithelial syncytium, i.e., syncytiotrophoblasts, differentiate from chorionic trophoblasts via cell fusion and separate maternal and fetal circulations in hemochorial placentas. L-type amino acid transporter 1 (LAT1) and its covalently linked ancillary subunit 4F2hc are colocalized on both maternal and fetal surfaces of syncytiotrophoblasts, implying their roles in amino acid transfer through the placental barrier. In this study, LAT1 knockout, in addition, revealed a novel role of LAT1 in syncytiotrophoblast development. LAT1 at midgestation was selectively expressed in trophoblastic lineages in the placenta, exclusively as a LAT1-4F2hc heterodimer. In LAT1 homozygous knockout mice, chorionic trophoblasts remained largely mononucleated, and the layers of syncytiotrophoblasts were almost completely absent. The amount of 4F2hc protein, which possesses a fusogenic function in trophoblastic cells, as well as in virus-infected cells, was drastically reduced by LAT1 knockout, with less affecting the mRNA level. Knockdown of LAT1 in trophoblastic BeWo cells also reduced 4F2hc protein and suppressed forskolin-induced cell fusion. These results demonstrate a novel fundamental role of LAT1 to support the protein expression of 4F2hc via a chaperone-like function in chorionic trophoblasts and to promote syncytiotrophoblast formation by contributing to cell fusion in the developing placenta.

Indexed as

AnimalsApoptosisCell FusionCell LineCell LineageCell ProliferationColforsinCrosses, GeneticEmbryo LossFemaleFusion Regulatory Protein 1, Heavy ChainGene DeletionGene Knockdown TechniquesGene TargetingHomozygoteHumansColforsinFusion Regulatory Protein 1, Heavy ChainLarge Neutral Amino Acid-Transporter 14F2 antigenamino acid transportercell fusionplacentasyncytiotrophoblast

Identifiers

PMID28320871
PMCPMC5440655
OpenAlexW2602229331

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.