Evidence map›Paper›PMID 21511332›Full record

ArticlePlacenta2011

Oxygen levels that optimize TSC culture are identified by maximizing growth rates and minimizing stress.

S Zhou, Y Xie, E E Puscheck, D A Rappolee

Abstract read
In one paragraph

Article in Placenta, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
4.4field-weighted citation impact, top 6% 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

28 citing papers in PubMed, 40 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Hypoxia and Placental Development.Birth defects research · 2017
    Review
  11. Article
  12. Review
  13. Departure from optimal OThe Journal of reproduction and development · 2017
    Article
  14. HIF-KDM3A-MMP12 regulatory circuit ensures trophoblast plasticity and placental adaptations to hypoxia.Proceedings of the National Academy of Sciences of the United States of America · 2016
    Article
  15. Article
  16. Article
  17. Comparison of 2, 5, and 20 % O2 on the development of post-thaw human embryos.Journal of assisted reproduction and genetics · 2016
    Article
  18. Article
  19. Article
  20. Review
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

4 authors at 1 institution in 1 country.

S ZhouCS Mott Center for Human Growth and Development, Wayne State University School of Medicine, Detroit, MI 48201, USA.
Y Xie
E E Puscheck
D A Rappolee
Wayne State University · US

Funding

SIGNALING PATHWAYS MEDIATING TROPHOBLAST PROLIFERATIONR01HD040972 · NICHD · WAYNE STATE UNIVERSITY · PI RAPPOLEE, DANIEL ALLEN · 2001 to 2005
$1.4M
AMP-activated protein kinase management will improve oocyte cryopreservationR03HD061431 · NICHD · WAYNE STATE UNIVERSITY · PI RAPPOLEE, DANIEL ALLEN · 2009 to 2010
$152k
NICHD NIH HHS 1R03HD061431 01NICHD NIH HHS R01 HD040972NICHD NIH HHS R03 HD061431
6 · The paper itself

Abstract

Accumulating data suggest that 20% O(2) causes human and mouse placental trophoblast stem cell (TSC) differentiation and suppresses proliferation. We tested the hypotheses that phosphorylated stress-activated protein kinase (pSAPK) levels report the optimal O(2) level for TSC culture, and that pSAPK responds to contradictory signals. We tested the dose range of 0-20% O(2) (0, 0.5, 2, and 20%) on five effects in cultured TSC. The results showed 1) TSC accumulation rates were highest at 2% O(2), lower at 20% and lowest at 0-0.5%; 2) pSAPK protein levels were lowest at 2% O(2), higher at 20%, and highest at 0-0.5%; 3) Cleaved caspase 3, an apoptosis marker, increased at 0.5% O(2), and was highest at 0% O(2); 4) Three markers for multipotency were highest at 2 and 20% and significantly decreased at 0.5%-0%; 5) In contrast three differentiation markers were lowest at 2% and highest at 0.5%-0%. Thus, 2% O(2) is the optimum as defined by lowest pSAPK and differentiation markers and highest growth rate and multipotency markers, without appreciable apoptosis. In addition, two lines of evidence suggest that fibroblast growth factor (FGF)4 does not directly activate SAPK. SAPK activity increases transiently with FGF4 removal at 2% O(2), but SAPK activity decreases when O(2) is switched from 20% to 2% with FGF4 present. Thus, SAPK is activated by contradictory signals, but activity decreases when either signal is removed. Taken together, the findings suggest that pSAPK senses suboptimal signals during TSC culture and probably in vivo.

Indexed as

AnimalsBlotting, WesternCells, CulturedFibroblast Growth Factor 4MiceMitogen-Activated Protein Kinase 11OxygenStem CellsStress, PhysiologicalTrophoblastsFGF4 protein, humanFibroblast Growth Factor 4Mitogen-Activated Protein Kinase 11Oxygen

Identifiers

PMID21511332
PMCPMC3096684
OpenAlexW1982348840

What OpenQuestion holds

Textmetadata
LicenceTDM
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.