Evidence map›Paper›PMID 36606407›Full record

ArticleDevelopmental dynamics : an official publication of the American Association of Anatomists2023

Characterizing the role of Pdgfra in calvarial development.

Meenakshi Umar, Garrett Bartoletti, Chunmin Dong, Apurva Gahankari, Danielle Browne, Alastair Deng, Josue Jaramillo, Mimi Sammarco, Jennifer Simkin, Fenglei He

Open access · greenAbstract read
In one paragraph

Article in Developmental dynamics : an official publication of the American Association of Anatomists, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.9field-weighted citation impact, top 21% 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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. Article
  3. Requirement of Pdgfrα+ cells for calvarial bone repair.Stem cells translational medicine · 2024
    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 at 2 institutions in 1 country.

Meenakshi UmarDepartment of Cell and Molecular Biology, School of Science and Engineering, Tulane University, New Orleans, Louisiana, USA.
Garrett BartolettiDepartment of Cell and Molecular Biology, School of Science and Engineering, Tulane University, New Orleans, Louisiana, USA.
Chunmin DongDepartment of Cell and Molecular Biology, School of Science and Engineering, Tulane University, New Orleans, Louisiana, USA.
Apurva GahankariDepartment of Cell and Molecular Biology, School of Science and Engineering, Tulane University, New Orleans, Louisiana, USA.
Danielle BrowneDepartment of Cell and Molecular Biology, School of Science and Engineering, Tulane University, New Orleans, Louisiana, USA.
Alastair DengDepartment of Cell and Molecular Biology, School of Science and Engineering, Tulane University, New Orleans, Louisiana, USA.
Josue JaramilloDepartment of Surgery, Tulane School of Medicine, New Orleans, Louisiana, USA.
Mimi SammarcoDepartment of Surgery, Tulane School of Medicine, New Orleans, Louisiana, USA.
Jennifer SimkinDepartment of Orthopaedic Surgery, Health Sciences Center, Louisiana State University, New Orleans, Louisiana, USA.
Fenglei HeDepartment of Cell and Molecular Biology, School of Science and Engineering, Tulane University, New Orleans, Louisiana, USA.ORCID 0000-0003-4717-8001
Tulane University · USLouisiana State University Health Sciences Center New Orleans · US

Funding

Molecular mechanisms of tissue interactions during coronal suture developmentR01DE028918 · NIDCR · TULANE UNIVERSITY OF LOUISIANA · PI HE, FENGLEI · 2019 to 2023
$1.8M
NIDCR NIH HHS R01 DE028918
6 · The paper itself

Abstract

backgroundMammalian calvarium is composed of flat bones developed from two origins, neural crest, and mesoderm. Cells from both origins exhibit similar behavior but express distinct transcriptomes. It is intriguing to ask whether genes shared by both origins play similar or distinct roles in development. In the present study, we have examined the role of Pdgfra, which is expressed in both neural crest and mesoderm, in specific lineages during calvarial development.

resultsWe found that in calvarial progenitor cells, Pdgfra is needed to maintain normal proliferation and migration of neural crest cells but only proliferation of mesoderm cells. Later in calvarial osteoblasts, we found that Pdgfra is necessary for both proliferation and differentiation of neural crest-derived cells, but not for differentiation of mesoderm-derived cells. We also examined the potential interaction between Pdgfra and other signaling pathway involved in calvarial osteoblasts but did not identify significant alteration of Wnt or Hh signaling activity in Pdgfra genetic models.

conclusionsPdgfra is required for normal calvarial development in both neural crest cells and mesoderm cells, but these lineages exhibit distinct responses to alteration of Pdgfra activity.

Indexed as

Receptor Protein-Tyrosine KinasesSkullAnimalsCell DifferentiationMammalsMesodermNeural CrestSignal TransductionReceptor Protein-Tyrosine Kinasescalvarialmesodermmouseneural crestosteoblastosteoprogenitorPdgfra

Identifiers

PMID36606407
PMCPMC10159935
OpenAlexW4313646664

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.