Evidence map›Paper›PMID 30540809›Full record

ArticlePloS one2018

A transient DMSO treatment increases the differentiation potential of human pluripotent stem cells through the Rb family.

Jingling Li, Cyndhavi Narayanan, Jing Bian, Danielle Sambo, Thomas Brickler, Wancong Zhang, Sundari Chetty

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 1 pooled it
1.3field-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, 1 synthesis or guideline pooled it, 27 citations in OpenAlex.

  1. Pooled it
  2. Autologous cord bloodWorld journal of clinical pediatrics · 2025
    Trial
  3. Article
  4. RosetteArraybioRxiv : the preprint server for biology · 2024
    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

7 authors at 1 institution in 1 country.

Jingling LiDepartment of Psychiatry and Behavioral Sciences, Stanford University School of Medicine, Stanford, California, United States of America.
Cyndhavi NarayananDepartment of Psychiatry and Behavioral Sciences, Stanford University School of Medicine, Stanford, California, United States of America.ORCID 0000-0001-8662-599X
Jing BianDepartment of Psychiatry and Behavioral Sciences, Stanford University School of Medicine, Stanford, California, United States of America.
Danielle SamboDepartment of Psychiatry and Behavioral Sciences, Stanford University School of Medicine, Stanford, California, United States of America.
Thomas BricklerDepartment of Psychiatry and Behavioral Sciences, Stanford University School of Medicine, Stanford, California, United States of America.
Wancong ZhangDepartment of Psychiatry and Behavioral Sciences, Stanford University School of Medicine, Stanford, California, United States of America.
Sundari ChettyDepartment of Psychiatry and Behavioral Sciences, Stanford University School of Medicine, Stanford, California, United States of America.ORCID 0000-0003-1940-9538
Stanford University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The propensity for differentiation varies substantially across human pluripotent stem cell (hPSC) lines, greatly restricting the use of hPSCs for cell replacement therapy or disease modeling. Here, we investigate the underlying mechanisms and demonstrate that activation of the retinoblastoma (Rb) pathway in a transient manner is important for differentiation. In prior work, we demonstrated that pre-treating hPSCs with dimethylsulfoxide (DMSO) before directed differentiation enhanced differentiation potential across all three germ layers. Here, we show that exposure to DMSO improves the efficiency of hPSC differentiation through Rb and by repressing downstream E2F-target genes. While transient inactivation of the Rb family members (including Rb, p107, and p130) suppresses DMSO's capacity to enhance differentiation across all germ layers, transient expression of a constitutively active (non-phosphorylatable) form of Rb increases the differentiation efficiency similar to DMSO. Inhibition of downstream targets of Rb, such as E2F signaling, also promotes differentiation of hPSCs. More generally, we demonstrate that the duration of Rb activation plays an important role in regulating differentiation capacity.

Indexed as

AminopyridinesCell Culture TechniquesCell DifferentiationCell LineDimethyl SulfoxideE2F Transcription FactorsGene Knockdown TechniquesGerm LayersHumansHydroxyquinolinesPluripotent Stem CellsRetinoblastoma-Like Protein p107Retinoblastoma-Like Protein p130Retinoblastoma ProteinSignal TransductionTime FactorsAminopyridinesDimethyl SulfoxideE2F Transcription FactorsHLM006474HydroxyquinolinesRetinoblastoma-Like Protein p107Retinoblastoma-Like Protein p130Retinoblastoma Protein

Identifiers

PMID30540809
PMCPMC6291069
OpenAlexW2904775560

What OpenQuestion holds

Textmetadata
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.