Evidence map›Paper›PMID 18032696›Full record

ArticleMolecular endocrinology (Baltimore, Md.)2008

The membrane-spanning domain of CD98 heavy chain promotes alpha(v)beta3 integrin signals in human extravillous trophoblasts.

Maryam Kabir-Salmani, Michiko N Fukuda, Masami Kanai-Azuma, Nesar Ahmed, Shigetatsu Shiokawa, Yoshihiro Akimoto, Keiji Sakai, Seishi Nagamori, Yoshikatsu Kanai, Kazuhiro Sugihara and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Molecular endocrinology (Baltimore, Md.), 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

15 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Endothelial Cells Require CD98 for Efficient Angiogenesis-Brief Report.Arteriosclerosis, thrombosis, and vascular biology · 2016
    Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Review
  13. Critical growth factors and signalling pathways controlling human trophoblast invasion.The International journal of developmental biology · 2010
    Review
  14. Article
  15. 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

11 authors at 3 institutions in 3 countries.

Maryam Kabir-SalmaniDepartment of Obstetrics and Gynecology, Kyorin University School of Medicine, shinkawa 6-20-2, Mitaka-shi, Tokyo 181-8611, Japan.
Michiko N Fukuda
Masami Kanai-Azuma
Nesar Ahmed
Shigetatsu Shiokawa
Yoshihiro Akimoto
Keiji Sakai
Seishi Nagamori
Yoshikatsu Kanai
Kazuhiro Sugihara
Mitsutoshi Iwashita
Kyorin University · JPNational Institute of Genetic Engineering and Biotechnology · IRSanford Burnham Prebys Medical Discovery Institute · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

CD98 heavy chain (CD98hc) is expressed highly in developing human placental trophoblast. CD98hc is an amino acid transporter and is thought to function in cell fusion, adhesion, and invasion by interacting with integrins. In invasive extravillous trophoblast, alpha(v)beta(3) integrin is expressed in a temporally and spatially specific manner, which prompted us to investigate the potential role of CD98hc in signal transduction of alpha(v)beta(3) integrin. Immunocytochemistry of extravillous trophoblast derived from human placenta revealed that CD98hc colocalized with alpha(v)beta(3) integrin and with alpha(v)beta(3)-associated cytoplasmic proteins including paxillin, vinculin, and focal adhesion kinase. Coimmunoprecipitation of CD98hc and its mutants revealed that the transmembrane domain of CD98hc is necessary for the association of CD98hc with alpha(v)beta(3) integrin. When CD98hc negative liver cells (FLC4) were stably transfected with CD98hc and the extracellular domain of CD98hc was cross-linked by anti-CD98 antibody, FLC4 cells binding affinity to fibronectin and cell motility increased. The anti-CD98 antibody cross-linking promoted actin stress fiber formation and activation of signal transduction downstream of RhoA GTPase, and elevated the phosphorylation of focal adhesion kinase, paxillin, and protein kinase B. Pretreatment of transfected FLC4 cells with specific inhibitors for alpha(v)beta(3)integrin, phosphatidylinositol 3-kinase, and RhoA diminished these effects caused by anti-CD98 antibody cross-linking. These results suggest that notoriously invasive activity of extravillous trophoblast is mediated by CD98hc, which promotes alpha(v)beta(3) integrin-dependent signals.

Indexed as

Biosensing TechniquesCell AdhesionCell LineCell MovementFemaleFibronectinsFocal Adhesion Protein-Tyrosine KinasesFusion Regulatory Protein 1, Heavy ChainHumansIntegrin alphaVbeta3Microscopy, Phase-ContrastPaxillinPhosphatidylinositol 3-KinasesPhosphorylationPlacentaPregnancyFibronectinsFocal Adhesion Protein-Tyrosine KinasesFusion Regulatory Protein 1, Heavy ChainIntegrin alphaVbeta3PaxillinPhosphatidylinositol 3-KinasesrhoA GTP-Binding ProteinVinculin

Identifiers

PMID18032696
PMCPMC5419622
OpenAlexW2162610604

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.