Evidence map›Paper›PMID 21275830›Full record

ArticleTissue engineering. Part A2011

Characterization and in vivo testing of mesenchymal stem cells derived from human embryonic stem cells.

William Gruenloh, Amal Kambal, Claus Sondergaard, Jeannine McGee, Catherine Nacey, Stefanos Kalomoiris, Karen Pepper, Scott Olson, Fernando Fierro, Jan A Nolta

Abstract read
In one paragraph

Article in Tissue engineering. Part A, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing 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

48 citing papers in PubMed.

  1. Article
  2. Mesenchymal stem cell therapy for pulmonary hypertension: an update.Frontiers in bioengineering and biotechnology · 2025
    Review
  3. Review
  4. Article
  5. Article
  6. Ex Vivo Mesenchymal Stem Cell Therapy to Regenerate Machine Perfused Organs.International journal of molecular sciences · 2021
    Review
  7. Article
  8. Review
  9. Review
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  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

10 authors.

William GruenlohStem Cell Program, Division of Hematology/Oncology, Department of Internal Medicine, University of California, Davis, Sacramento, California 95817, USA.
Amal Kambal
Claus Sondergaard
Jeannine McGee
Catherine Nacey
Stefanos Kalomoiris
Karen Pepper
Scott Olson
Fernando Fierro
Jan A Nolta

Funding

Staff InvestigatorsP30CA093373 · NCI · UNIVERSITY OF CALIFORNIA DAVIS · PI Laura Marcu · 2002 to 2026
$84.9M
Immunodeficient Mouse Model of Stem Cell PlasticityR01DK061848 · NIDDK · WASHINGTON UNIVERSITY · PI NOLTA, JAN A. · 2001 to 2009
$2.7M
Functional dissection of human A-MSC vs BM-MSC phenotypeR01HL073256 · NHLBI · WASHINGTON UNIVERSITY · PI NOLTA, JAN A. · 2003 to 2010
$2.3M
EX VIVO STEM CELL MANIPULATION AND HUMAN HEMATOPOIESISR01DK053041 · NIDDK · WASHINGTON UNIVERSITY · PI NOLTA, JAN A. · 1998 to 2006
$1.6M
NCI NIH HHS P30 CA093373NHLBI NIH HHS R01HL073256NIDDK NIH HHS 2R01DK53041NIDDK NIH HHS 2R01DK61848
6 · The paper itself

Abstract

Mesenchymal stem cells (MSCs) have been shown to contribute to the recovery of tissues through homing to injured areas, especially to hypoxic, apoptotic, or inflamed areas and releasing factors that hasten endogenous repair. In some cases genetic engineering of the MSC is desired, since they are excellent delivery vehicles. We have derived MSCs from the human embryonic stem cell (hESC) line H9 (H9-MSCs). They expressed CD105, CD90, CD73, and CD146, and lacked expression of CD45, CD34, CD14, CD31, and HLA-DR, the hESC pluripotency markers SSEA-4 and Tra-1-81, and the hESC early differentiation marker SSEA-1. Marrow-derived MSCs showed a similar phenotype. H9-MSCs did not form teratoma in our initial studies, whereas the parent H9 line did so robustly. H9-MSCs differentiated into bone, cartilage, and adipocytes in vitro, and displayed increased migration under hypoxic conditions. Finally, using a hindlimb ischemia model, H9-MSCs were shown to home to the hypoxic muscle, but not the contralateral limb, by 48 h after IV injection. In summary, we have defined methods for differentiation of hESCs into MSCs and have defined their characteristics and in vivo migratory properties.

Indexed as

AnimalsCell Culture TechniquesCell DifferentiationCell HypoxiaCell LineCell LineageCell MovementCells, CulturedCell ShapeEmbryonic Stem CellsFlow CytometryHindlimbHumansIschemiaKaryotypingMesenchymal Stem Cells

Identifiers

PMID21275830
PMCPMC3099448

What OpenQuestion holds

Textmetadata
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.