Evidence map›Paper›PMID 28463594›Full record

ArticleTissue engineering. Part A2018

Effects of WNT3A and WNT16 on the Osteogenic and Adipogenic Differentiation of Perivascular Stem/Stromal Cells.

Jia Shen, Xuepeng Chen, Haichao Jia, Carolyn A Meyers, Swati Shrestha, Greg Asatrian, Catherine Ding, Rebecca Tsuei, Xinli Zhang, Bruno Peault and 3 more

Open access · greenAbstract read
In one paragraph

Article in Tissue engineering. Part A, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

16 citing papers in PubMed, 27 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. The role of wnt signaling in diabetes-induced osteoporosis.Diabetology & metabolic syndrome · 2023
    Review
  6. Article
  7. Article
  8. Review
  9. Review
  10. Roles of Non-Canonical Wnt Signalling Pathways in Bone Biology.International journal of molecular sciences · 2021
    Review
  11. Article
  12. Sirtuin-1 and Its Relevance in Vascular Calcification.International journal of molecular sciences · 2020
    Review
  13. Five Decades Later, Are Mesenchymal Stem Cells Still Relevant?Frontiers in bioengineering and biotechnology · 2020
    Review
  14. Article
  15. Perivascular Mesenchymal Progenitors for Bone Regeneration.Journal of orthopaedic research : official publication of the Orthopaedic Research Society · 2019
    Review
  16. 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

13 authors at 4 institutions in 3 countries.

Jia Shen1 Division of Growth and Development and Section of Orthodontics, School of Dentistry, UCLA , Los Angeles, California.
Xuepeng Chen2 Department of Orthodontics, Stomatological Hospital, Zhejiang University , Hangzhou, China .
Haichao Jia3 Department of Orthodontics, School of Stomatology, Capital Medical University , Beijing, China .
Carolyn A Meyers4 Department of Pathology, Johns Hopkins University , Baltimore, Maryland.
Swati Shrestha1 Division of Growth and Development and Section of Orthodontics, School of Dentistry, UCLA , Los Angeles, California.
Greg Asatrian1 Division of Growth and Development and Section of Orthodontics, School of Dentistry, UCLA , Los Angeles, California.
Catherine Ding1 Division of Growth and Development and Section of Orthodontics, School of Dentistry, UCLA , Los Angeles, California.
Rebecca Tsuei1 Division of Growth and Development and Section of Orthodontics, School of Dentistry, UCLA , Los Angeles, California.
Xinli Zhang1 Division of Growth and Development and Section of Orthodontics, School of Dentistry, UCLA , Los Angeles, California.
Bruno Peault5 Department of Orthopaedic Surgery, UCLA and Orthopaedic Hospital, Orthopaedic Hospital Research Center , Los Angeles, California.
Kang Ting1 Division of Growth and Development and Section of Orthodontics, School of Dentistry, UCLA , Los Angeles, California.
Chia Soo5 Department of Orthopaedic Surgery, UCLA and Orthopaedic Hospital, Orthopaedic Hospital Research Center , Los Angeles, California.
Aaron W James4 Department of Pathology, Johns Hopkins University , Baltimore, Maryland.
Johns Hopkins University · USCapital Medical University · CNMRC Centre for Regenerative Medicine · GBUniversity of California, Los Angeles · US

Funding

NELL-1 Systemic Therapy for OsteoporosisR01AR066782 · NIAMS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI EASLEY, JEREMIAH, TING, KANG · 2014 to 2018
$2.0M
Wnt and PPARy Signaling in Nell-1 and BMP2 Mediated Bone RegenerationR01AR061399 · NIAMS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI SOO, CHIA · 2012 to 2016
$1.7M
Direct and indirect contributions of perivascular stem cells to bone healingR01AR070773 · NIAMS · JOHNS HOPKINS UNIVERSITY · PI JAMES, AARON W · 2017 to 2021
$1.4M
NELL-1 isoforms for the systemic treatment of osteoporosisK08AR068316 · NIAMS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI JAMES, AARON W · 2015 to 2019
$534k
Medical Research Council G1000816NIAMS NIH HHS K08 AR068316NIAMS NIH HHS R01 AR061399NIAMS NIH HHS R01 AR066782NIAMS NIH HHS R01 AR070773
6 · The paper itself

Abstract

Human perivascular stem/stromal cells (hPSC) are a multipotent mesenchymogenic stromal cell population defined by their perivascular locale. Recent studies have demonstrated the high potential for clinical translation of this fluorescence-activated cell sorting (FACS)-derived cell population for autologous bone tissue engineering. However, the mechanisms underlying the osteogenic differentiation of PSC are incompletely understood. The current study investigates the roles of canonical and noncanonical Wnt signaling in the osteogenic and adipogenic differentiation of PSC. Results showed that both canonical and noncanonical Wnt signaling activity transiently increased during PSC osteogenic differentiation in vitro. Sustained WNT3A treatment significantly decreased PSC osteogenic differentiation. Conversely, sustained treatment with Wnt family member 16 (WNT16), a mixed canonical and noncanonical ligand, increased osteogenic differentiation in a c-Jun N-terminal kinase (JNK) pathway-dependent manner. Conversely, WNT16 knockdown significantly diminished PSC osteogenic differentiation. Finally, WNT16 but not WNT3A increased the adipogenic differentiation of PSC. These results indicate the importance of regulation of canonical and noncanonical Wnt signaling for PSC fate and differentiation. Moreover, these data suggest that WNT16 plays a functional and necessary role in PSC osteogenesis.

Indexed as

AdipogenesisCell DifferentiationCells, CulturedHumansMesenchymal Stem CellsOsteogenesisStromal CellsTissue EngineeringWnt3A ProteinWnt ProteinsWnt Signaling PathwayWnt3A ProteinWnt ProteinsDKK1osteogenesisperivascular stem cellPSCWNT16WNT3AWnt signaling

Identifiers

PMID28463594
PMCPMC5770092
OpenAlexW2610527917

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.