Evidence map›Paper›PMID 32369556›Full record

ReviewBiochemical Society transactions2020

The emerging complexity of PDGFRs: activation, internalization and signal attenuation.

Madison A Rogers, Katherine A Fantauzzo

Abstract readReview
In one paragraph

Review in Biochemical Society transactions, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing 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

31 citing papers in PubMed.

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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

2 authors.

Madison A RogersDepartment of Craniofacial Biology, School of Dental Medicine, University of Colorado Anschutz Medical Campus, Aurora, CO, U.S.A.
Katherine A FantauzzoDepartment of Craniofacial Biology, School of Dental Medicine, University of Colorado Anschutz Medical Campus, Aurora, CO, U.S.A.

Funding

Characterization of PDGFR dimer-specific dynamics in the craniofacial mesenchymeR01DE027689 · NIDCR · UNIVERSITY OF COLORADO DENVER · PI FANTAUZZO, KATHERINE ANN · 2018 to 2022
$2.0M
Characterization of PDGFR dimer-specific dynamics in the craniofacial mesenchymeK02DE028572 · NIDCR · UNIVERSITY OF COLORADO DENVER · PI FANTAUZZO, KATHERINE ANN · 2019 to 2023
$627k
NIDCR NIH HHS K02 DE028572NIDCR NIH HHS R01 DE027689
6 · The paper itself

Abstract

The platelet-derived growth factor receptor (PDGFR) family of receptor tyrosine kinases allows cells to communicate with the environment to regulate diverse cellular activities. Here, we highlight recent data investigating the structural makeup of individual PDGFRs upon activation, revealing the importance of the whole receptor in the propagation of extracellular ligand binding and dimerization. Furthermore, we review ongoing research demonstrating the significance of receptor internalization and signal attenuation in the regulation of PDGFR activity. Interactions with internalization machinery, signaling from endosomes, receptor degradation and receptor recycling are physiological means by which cells fine-tune PDGFR responses to growth factor stimulation. In this review, we discuss the biophysical, structural, in silico and biochemical data that have provided evidence for these mechanisms. We further highlight the commonalities and differences between PDGFRα and PDGFRβ signaling, revealing critical gaps in knowledge. In total, this review provides a conclusive summary on the state of the PDGFR field and underscores the need for novel techniques to fully elucidate the mechanisms of PDGFR activation, internalization and signal attenuation.

Indexed as

LigandsSignal TransductionAmino Acid MotifsAnimalsComputer SimulationEndosomesHumansPhosphorylationProtein MultimerizationReceptor, Platelet-Derived Growth Factor alphaReceptor, Platelet-Derived Growth Factor betaReceptor Protein-Tyrosine KinasesLigandsPDGFRB protein, humanReceptor, Platelet-Derived Growth Factor alphaReceptor, Platelet-Derived Growth Factor betaReceptor Protein-Tyrosine KinasesPDGFRRTKsignaling

Identifiers

PMID32369556
PMCPMC7722362

What Socratic 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 Socratic graph.