Evidence map›Paper›PMID 24372153›Full record

ArticleStem cells and development2014

Human and murine very small embryonic-like cells represent multipotent tissue progenitors, in vitro and in vivo.

Aaron M Havens, Hongli Sun, Yusuke Shiozawa, Younghun Jung, Jingcheng Wang, Anjali Mishra, Yajuan Jiang, David W O'Neill, Paul H Krebsbach, Denis O Rodgerson and 1 more

Abstract read
In one paragraph

Article in Stem cells and development, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers.

0numbers the graph read from it
0cells of the map it votes in
55citing 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

55 citing papers in PubMed.

  1. Trial
  2. Article
  3. Review
  4. Review
  5. Review
  6. Article
  7. Article
  8. CD34 positive cells as endothelial progenitor cells in biology and medicine.Frontiers in cell and developmental biology · 2023
    Review
  9. Article
  10. Article
  11. Article
  12. Human CD34Leukemia · 2022
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Review
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

11 authors.

Aaron M Havens1 Department of Periodontics and Oral Medicine, University of Michigan , School of Dentistry, Ann Arbor, Michigan.
Hongli Sun
Yusuke Shiozawa
Younghun Jung
Jingcheng Wang
Anjali Mishra
Yajuan Jiang
David W O'Neill
Paul H Krebsbach
Denis O Rodgerson
Russell S Taichman

Funding

Tissue Engineering and RegenerationT32DE007057 · NIDCR · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI DAVID H. KOHN · 1985 to 2026
$17.3M
FunctionalCharacterization of the Stem Cell NicheR01DK082481 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI KREBSBACH, PAUL HUGO, TAICHMAN, RUSSELL S · 2009 to 2012
$1.4M
Repair of Bone Defects with Human Autologous Pluripotent Very Small Embryonic likR44DE022493 · NIDCR · LISATA THERAPEUTICS INC · PI MCCAULEY, LAURIE K., RODGERSON, DENIS OVEREND · 2012 to 2012
$412k
NIAMS NIH HHS AR0568903NIDCR NIH HHS DE022493NIDCR NIH HHS T32 DE007057NIDDK NIH HHS DK082481
6 · The paper itself

Abstract

The purpose of this study was to determine the lineage progression of human and murine very small embryonic-like (HuVSEL or MuVSEL) cells in vitro and in vivo. In vitro, HuVSEL and MuVSEL cells differentiated into cells of all three embryonic germ layers. HuVSEL cells produced robust mineralized tissue of human origin compared with controls in calvarial defects. Immunohistochemistry demonstrated that the HuVSEL cells gave rise to neurons, adipocytes, chondrocytes, and osteoblasts within the calvarial defects. MuVSEL cells were also able to differentiate into similar lineages. First round serial transplants of MuVSEL cells into irradiated osseous sites demonstrated that ∼60% of the cells maintained their VSEL cell phenotype while other cells differentiated into multiple tissues at 3 months. Secondary transplants did not identify donor VSEL cells, suggesting limited self renewal but did demonstrate VSEL cell derivatives in situ for up to 1 year. At no point were teratomas identified. These studies show that VSEL cells produce multiple cellular structures in vivo and in vitro and lay the foundation for future cell-based regenerative therapies for osseous, neural, and connective tissue disorders.

Indexed as

AdipocytesAnimalsBiomarkersBone RegenerationCell DifferentiationCell LineageCells, CulturedCell SeparationCell SizeChondrocytesEmbryonic Stem CellsFemaleHumansMaleMiceMice, SCIDBiomarkers

Identifiers

PMID24372153
PMCPMC3967374

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.