Evidence map›Paper›PMID 26042795›Full record

ArticleStem cell research2015

Chemically-defined albumin-free differentiation of human pluripotent stem cells to endothelial progenitor cells.

Xiaoping Bao, Xiaojun Lian, Kaitlin K Dunn, Mengxuan Shi, Tianxiao Han, Tongcheng Qian, Vijesh J Bhute, Scott G Canfield, Sean P Palecek

Abstract read
In one paragraph

Article in Stem cell research, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
–field-weighted citation impact
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

46 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Review
  9. Review
  10. Engineering approaches for cardiac organoid formation and their characterization.Translational research : the journal of laboratory and clinical medicine · 2022
    Review
  11. Article
  12. Stem cell-mediated angiogenesis in skin tissue engineering and wound healing.Wound repair and regeneration : official publication of the Wound Healing Society [and] the European Tissue Repair Society · 2022
    Review
  13. Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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

9 authors.

Xiaoping Bao *Department of Chemical & Biological Engineering, University of Wisconsin, Madison, WI 53706, USA.
Xiaojun Lian *Department of Chemical & Biological Engineering, University of Wisconsin, Madison, WI 53706, USA.
Kaitlin K DunnDepartment of Chemical & Biological Engineering, University of Wisconsin, Madison, WI 53706, USA.
Mengxuan ShiDepartment of Chemical & Biological Engineering, University of Wisconsin, Madison, WI 53706, USA.
Tianxiao HanDepartment of Chemical & Biological Engineering, University of Wisconsin, Madison, WI 53706, USA.
Tongcheng QianDepartment of Chemical & Biological Engineering, University of Wisconsin, Madison, WI 53706, USA.
Vijesh J BhuteDepartment of Chemical & Biological Engineering, University of Wisconsin, Madison, WI 53706, USA.
Scott G CanfieldDepartment of Chemical & Biological Engineering, University of Wisconsin, Madison, WI 53706, USA.
Sean P PalecekDepartment of Chemical & Biological Engineering, University of Wisconsin, Madison, WI 53706, USA.

Funding

Chemistry-Biology Interface Training ProgramT32GM008505 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI BLACKWELL, HELEN E. · 1993 to 2023
$9.8M
Regulating human pluripotent stem cell differentiation by colony confinementR01EB007534 · NIBIB · UNIVERSITY OF WISCONSIN-MADISON · PI PALECEK, SEAN P · 2007 to 2019
$4.1M
Shear regulated differentiation of hPSCs to brain endothelial cellsR21NS085351 · NINDS · UNIVERSITY OF WISCONSIN-MADISON · PI PALECEK, SEAN P · 2013 to 2014
$407k
NIBIB NIH HHS R01 EB007534NIGMS NIH HHS T32 GM008505NINDS NIH HHS R21 NS085351NINDS NIH HHS R21NS085351
6 · The paper itself

Abstract

Human pluripotent stem cell (hPSC)-derived endothelial cells and their progenitors are important for vascular research and therapeutic revascularization. Here, we report a completely defined endothelial progenitor differentiation platform that uses a minimalistic medium consisting of Dulbecco's modified eagle medium and ascorbic acid, lacking of albumin and growth factors. Following hPSC treatment with a GSK-3β inhibitor and culture in this medium, this protocol generates more than 30% multipotent CD34+ CD31+ endothelial progenitors that can be purified to >95% CD34+ cells via magnetic activated cell sorting (MACS). These CD34+ progenitors are capable of differentiating into endothelial cells in serum-free inductive media. These hPSC-derived endothelial cells express key endothelial markers including CD31, VE-cadherin, and von Willebrand factor (vWF), exhibit endothelial-specific phenotypes and functions including tube formation and acetylated low-density lipoprotein (Ac-LDL) uptake. This fully defined platform should facilitate production of proliferative, xeno-free endothelial progenitor cells for both research and clinical applications.

Indexed as

Cell DifferentiationAlbuminsAntigens, CDCulture MediaEndothelial Progenitor CellsHumansMultipotent Stem CellsPluripotent Stem CellsAlbuminsAntigens, CDCulture Media

Identifiers

PMID26042795
PMCPMC4516678

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.