Evidence map›Paper›PMID 26252772›Full record

ArticlePloS one2015

Promotion of Erythropoietic Differentiation in Hematopoietic Stem Cells by SOCS3 Knock-Down.

Yu-xiao Liu, Xing Dong, Feng Gong, Ning Su, Su-bo Li, Hai-tao Zhang, Jia-ling Liu, Jing-hui Xue, Shou-ping Ji, Zhi-wen Zhang

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.7field-weighted citation impact, top 28% 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

7 citing papers in PubMed, 8 citations in OpenAlex.

  1. RNA mNature · 2024
    Article
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  3. Indoxyl sulfate impairsExperimental biology and medicine (Maywood, N.J.) · 2022
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  4. Article
  5. 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

10 authors at 2 institutions in 1 country.

Yu-xiao LiuFirst Affiliated Hospital of Chinese PLA General Hospital, Beijing, China.
Xing DongThird Military Medical University, Chongqing, China; General Hospital of Beijing Military Command, Beijing, China.
Feng GongBeijing Institution of Transfusion Medicine, Beijing, China.
Ning SuFirst Affiliated Hospital of Chinese PLA General Hospital, Beijing, China.
Su-bo LiBeijing Institution of Transfusion Medicine, Beijing, China.
Hai-tao ZhangFirst Affiliated Hospital of Chinese PLA General Hospital, Beijing, China.
Jia-ling LiuFirst Affiliated Hospital of Chinese PLA General Hospital, Beijing, China.
Jing-hui XueFirst Affiliated Hospital of Chinese PLA General Hospital, Beijing, China.
Shou-ping JiBeijing Institution of Transfusion Medicine, Beijing, China.
Zhi-wen ZhangFirst Affiliated Hospital of Chinese PLA General Hospital, Beijing, China.
First Affiliated Hospital of Chinese PLA General Hospital · CNArmy Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Suppressor of cytokine signaling 3 (SOCS3) plays an important role in mice fetal liver erythropoiesis, but the roles of SOCS3 in human hematopoietic stem cells (HSCs) have not been well investigated. In the present study, lentiviral small interference RNA expression vectors (shRNA) of SOCS3 were constructed and stably transferred into HSCs. We found that SOCS3 knockdown induced erythroid expansion in HSCs. Conversely, Ectopic expression of SOCS3 in progenitor cells blocked erythroid expansion and erythroid colony formation of HSCs. To further explore the involved mechanism, we compared gene expression profiles of SOCS3-shRNA tranduced HSCs with that of control HSCs by whole genome microarrays. The results indicated that cell developmental process related genes, especially hematopoietic lineage-specific genes, associated with the responses to SOCS3 in HSCs.Downexpression of SOCS3 in HSCs or differentiated erythroid progenitor cells induced a transcriptional program enriched for erythroid development relative genes. Our results proved that SOCS3 down-expression induced lineage commitment towards erythroid progenitor cell fate by activation of erythroid-specific gene in HSCs and provided new insight into the mechanism of erythropoietic development.

Indexed as

Antigens, CD34Cell Culture TechniquesCell DifferentiationCell LineageCells, CulturedCell SeparationErythroid Precursor CellsFetal BloodFlow CytometryGene Expression ProfilingGene Expression RegulationGene Knockdown TechniquesGenome, HumanHematopoietic Stem CellsHemoglobinsHumansAntigens, CD34HemoglobinsRNA, Small InterferingSOCS3 protein, humanSuppressor of Cytokine Signaling 3 ProteinSuppressor of Cytokine Signaling Proteins

Identifiers

PMID26252772
PMCPMC4529111
OpenAlexW1200695084

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.