Evidence map›Paper›PMID 33656760›Full record

ArticleCell proliferation2021

Vitronectin-activated αvβ3 and αvβ5 integrin signalling specifies haematopoietic fate in human pluripotent stem cells.

Jun Shen, Yaoyao Zhu, Shuo Zhang, Shuzhen Lyu, Cuicui Lyu, Zicen Feng, Dixie L Hoyle, Zack Z Wang, Tao Cheng

Open access · goldAbstract read
In one paragraph

Article in Cell proliferation, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
3.4field-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

18 citing papers in PubMed, 37 citations in OpenAlex.

  1. Article
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  6. iScience · 2024
    Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Review
  12. CSK-mediated signalling by integrins in cancer.Frontiers in cell and developmental biology · 2023
    Review
  13. Article
  14. Article
  15. Article
  16. Review
  17. 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

9 authors at 5 institutions in 2 countries.

Jun ShenState Key Laboratory of Experimental Hematology, National Clinical Research Center for Blood Diseases, Institute of Hematology & Blood Diseases Hospital, Chinese Academy of Medical Science & Peking Union Medical College, Tianjin, China.ORCID https://orcid.org/0000-0002-8319-8213
Yaoyao ZhuState Key Laboratory of Experimental Hematology, National Clinical Research Center for Blood Diseases, Institute of Hematology & Blood Diseases Hospital, Chinese Academy of Medical Science & Peking Union Medical College, Tianjin, China.
Shuo ZhangState Key Laboratory of Experimental Hematology, National Clinical Research Center for Blood Diseases, Institute of Hematology & Blood Diseases Hospital, Chinese Academy of Medical Science & Peking Union Medical College, Tianjin, China.
Shuzhen LyuState Key Laboratory of Experimental Hematology, National Clinical Research Center for Blood Diseases, Institute of Hematology & Blood Diseases Hospital, Chinese Academy of Medical Science & Peking Union Medical College, Tianjin, China.
Cuicui LyuDepartment of Hematology, the First Central Hospital of Tianjin, Tianjin, China.
Zicen FengCenter of Reproductive Medicine, Tianjin Central Hospital of Gynaecology and Obstetrics, Tianjin, China.
Dixie L HoyleDivision of Hematology, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Zack Z WangDivision of Hematology, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Tao ChengState Key Laboratory of Experimental Hematology, National Clinical Research Center for Blood Diseases, Institute of Hematology & Blood Diseases Hospital, Chinese Academy of Medical Science & Peking Union Medical College, Tianjin, China.
Institute of Hematology & Blood Diseases Hospital · CNJohns Hopkins University · USPeking Union Medical College Hospital · CNTianjin Central Hospital of Gynecology Obstetrics · CNTianjin First Center Hospital · CN

Funding

Generation of engraftable HSPCs from hemogenic endothelial cellsR01DK106109 · NIDDK · JOHNS HOPKINS UNIVERSITY · PI WANG, ZACK Z. · 2016 to 2018
$875k
CAMS Innovation Fund for Medical Sciences 2016-I2M-1-017CAMS Innovation Fund for Medical Sciences 2019-I2M-1-006National Institute of Diabetes and Digestive and Kidney Disease R01DK106109National Key Research and Development Program of China Stem Cell and Translational Research 2016YFA0100600National Key Research and Development Program of China Stem Cell and Translational Research 2017YFA0103102National Key Research and Development Program of China Stem Cell and Translational Research 2017YFA0103400National Key Research and Development Program of China Stem Cell and Translational Research 2019YFA0110204National Natural Science Foundation of China 81421002National Natural Science Foundation of China 81900186National Natural Science Foundation of China 82000118NIDDK NIH HHS R01 DK106109NIH HHS
6 · The paper itself

Abstract

objectivesVitronectin (VTN) has been widely used for the maintenance and expansion of human pluripotent stem cells (hPSCs) as feeder-free conditions. However, the effect of VTN on hPSC differentiation remains unclear. Here, we investigated the role of VTN in early haematopoietic development of hPSCs. MATERIALS AND

methodsA chemically defined monolayer system was applied to study the role of different matrix or basement membrane proteins in haematopoietic development of hPSCs. The role of integrin signalling in VTN-mediated haematopoietic differentiation was investigated by integrin antagonists. Finally, small interfering RNA was used to knock down integrin gene expression in differentiated cells.

resultsWe found that the haematopoietic differentiation of hPSCs on VTN was far more efficient than that on Matrigel that is also often used for hPSC culture. VTN promoted the fate determination of endothelial-haematopoietic lineage during mesoderm development to generate haemogenic endothelium (HE). Moreover, we demonstrated that the signals through αvβ3 and αvβ5 integrins were required for VTN-promoted haematopoietic differentiation. Blocking αvβ3 and αvβ5 integrins by the integrin antagonists impaired the development of HE, but not endothelial-to-haematopoietic transition (EHT). Finally, both αvβ3 and αvβ5 were confirmed acting synergistically for early haematopoietic differentiation by knockdown the expression of αv, β3 or β5.

conclusionThe established VTN-based monolayer system of haematopoietic differentiation of hPSCs presents a valuable platform for further investigating niche signals involved in human haematopoietic development.

Indexed as

Cell AdhesionCell DifferentiationCell LineGene Expression RegulationHematopoietic Stem CellsHomeodomain ProteinsHumansIntegrin alphaVbeta3MesodermPluripotent Stem CellsReceptors, VitronectinRNA InterferenceRNA, Small InterferingSignal TransductionSnake VenomsVitronectinCilengitideHomeodomain ProteinsIntegrin alphaVbeta3integrin alphaVbeta5MIXL1 protein, humanReceptors, VitronectinRNA, Small InterferingSnake VenomsVitronectinextracellular matrixhaematopoietic differentiationhuman pluripotent stem cellsintegrinvitronectin

Identifiers

PMID33656760
PMCPMC8016644
OpenAlexW3135218296

What OpenQuestion holds

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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.