Evidence map›Paper›PMID 30340089›Full record

ArticleStem cell research2018

Derivation and characterization of putative craniofacial mesenchymal progenitor cells from human induced pluripotent stem cells.

Mohamed Jamal, Sara L Lewandowski, Matthew L Lawton, George T-J Huang, Laertis Ikonomou

Open access · goldAbstract read
In one paragraph

Article in Stem cell research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.3field-weighted citation impact, top 19% 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

11 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. The Progress of Stem Cell Technology for Skeletal Regeneration.International journal of molecular sciences · 2021
    Review
  10. Review
  11. 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

5 authors at 2 institutions in 1 country.

Mohamed JamalCenter for Regenerative Medicine, Boston University and Boston Medical Center, Boston, MA, USA.
Sara L LewandowskiCenter for Regenerative Medicine, Boston University and Boston Medical Center, Boston, MA, USA.
Matthew L LawtonCenter for Regenerative Medicine, Boston University and Boston Medical Center, Boston, MA, USA.
George T-J HuangDepartment of Bioscience Research, College of Dentistry, University of Tennessee Health Science Center, Memphis, TN, USA.
Laertis IkonomouCenter for Regenerative Medicine, Boston University and Boston Medical Center, Boston, MA, USA; Pulmonary Center, Boston University School of Medicine, Boston, MA, USA. Electronic address: laertis@bu.edu.
Boston University · USUniversity of Tennessee Health Science Center · US

Funding

Project-005UL1TR001430 · NCATS · BOSTON UNIVERSITY MEDICAL CAMPUS · PI BAIR-MERRITT, MEGAN H, CENTER, DAVID M. · 2015 to 2024
$52.3M
A National iPS Cell Network with Deep Phenotyping for Translational ResearchU01TR001810 · NCATS · BOSTON UNIVERSITY MEDICAL CAMPUS · PI GILAD, YOAV, KOTTON, DARRELL N. · 2016 to 2020
$4.4M
NRSA Training CoreTL1TR001410 · NCATS · BOSTON UNIVERSITY MEDICAL CAMPUS · PI KOTTON, DARRELL N. · 2015 to 2024
$4.3M
A National Resource for Lung disease-specific iPS cellsR24HL123828 · NHLBI · BOSTON UNIVERSITY MEDICAL CAMPUS · PI KOTTON, DARRELL N., MOSTOSLAVSKY, GUSTAVO · 2014 to 2018
$2.7M
Defining the genetic program of primordial lung progenitorsR01HL111574 · NHLBI · BOSTON UNIVERSITY MEDICAL CAMPUS · PI IKONOMOU, LAERTIS · 2012 to 2016
$2.1M
Stem Cell Based Therapy for Regenerative Endodontics R01DE019156 · NIDCR · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI HUANG, GEORGE T.J · 2008 to 2013
$1.8M
Biomechanical determinants of lung cell fate in pluripotent stem cellsR01HL124280 · NHLBI · BOSTON UNIVERSITY MEDICAL CAMPUS · PI IKONOMOU, LAERTIS, WONG, JOYCE Y · 2014 to 2017
$1.6M
NCATS NIH HHS TL1 TR001410NCATS NIH HHS U01 TR001810NCATS NIH HHS UL1 TR001430NHLBI NIH HHS R01 HL111574NHLBI NIH HHS R01 HL124280NHLBI NIH HHS R24 HL123828NIDCR NIH HHS R01 DE019156
6 · The paper itself

Abstract

The introduction and widespread adoption of induced pluripotent stem cell (iPSC) technology has opened new avenues for craniofacial regenerative medicine. Neural crest cells (NCCs) are the precursor population to many craniofacial structures, including dental and periodontal structures, and iPSC-derived NCCs may, in the near future, offer an unlimited supply of patient-specific cells for craniofacial repair interventions. Here, we used an established protocol involving simultaneous Wnt signaling activation and TGF-β signaling inhibition to differentiate three human iPSC lines to cranial NCCs. We then derived a mesenchymal progenitor cell (NCC-MPCs) population with chondrogenic and osteogenic potential from cranial NCCs and investigated their similarity to widely studied human postnatal dental or periodontal stem/progenitor cells. NCC-MPCs were quite distinct from both their precursor cells (NCCs) and bone-marrow mesenchymal stromal cells, a stromal population of mesodermal origin. Despite their similarity with dental stem/progenitor cells, NCC-MPCs were clearly differentiated by a core set of 43 genes, including ACKR3 (CXCR7), whose expression (both at transcript and protein level) appear to be specific to NCC-MPCs. Altogether, our data demonstrate the feasibility of craniofacial mesenchymal progenitor derivation from human iPSCs through a neural crest-intermediate and set the foundation for future studies regarding their full differentiation repertoire and their in vivo existence.

Indexed as

Cell DifferentiationCraniofacial AbnormalitiesHumansInduced Pluripotent Stem CellsMesenchymal Stem Cells

Identifiers

PMID30340089
PMCPMC6294687
OpenAlexW2897045333

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.