Evidence map›Paper›PMID 35977484›Full record

ArticleCell reports2022

Temporal control of PDGFRα regulates the fibroblast-to-myofibroblast transition in wound healing.

Longbiao Yao, Bharath H Rathnakar, Hae Ryong Kwon, Hiromi Sakashita, Jang H Kim, Alex Rackley, James J Tomasek, William L Berry, Lorin E Olson

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed, 1 pooled it
6.2field-weighted citation impact, top 3% 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

55 citing papers in PubMed, 1 synthesis or guideline pooled it, 68 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Macrophage-Derived Extracellular Vesicles Deliver Progranulin to Alleviate Skin Wound Fibrosis.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
    Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Single-Cell Sequencing Reveals That CCL2+ Adipose-Derived Stem Cells Promote Diabetic Wound Healing Through the CCL2-ACKR1 Signaling Axis.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
    Article
  10. Article
  11. Review
  12. Review
  13. Article
  14. CAR-T cell immunotherapy in rhabdomyosarcoma.Journal of translational medicine · 2026
    Review
  15. Article
  16. Article
  17. Review
  18. Article
  19. Article
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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

9 authors at 2 institutions in 1 country.

Longbiao YaoCardiovascular Biology Research Program, Oklahoma Medical Research Foundation, Oklahoma City, OK 73104, USA.
Bharath H RathnakarCardiovascular Biology Research Program, Oklahoma Medical Research Foundation, Oklahoma City, OK 73104, USA.
Hae Ryong KwonCardiovascular Biology Research Program, Oklahoma Medical Research Foundation, Oklahoma City, OK 73104, USA.
Hiromi SakashitaCardiovascular Biology Research Program, Oklahoma Medical Research Foundation, Oklahoma City, OK 73104, USA.
Jang H KimCardiovascular Biology Research Program, Oklahoma Medical Research Foundation, Oklahoma City, OK 73104, USA; Department of Cell Biology, University of Oklahoma Health Sciences Center, Oklahoma City, OK 73104, USA.
Alex RackleyCardiovascular Biology Research Program, Oklahoma Medical Research Foundation, Oklahoma City, OK 73104, USA.
James J TomasekDepartment of Cell Biology, University of Oklahoma Health Sciences Center, Oklahoma City, OK 73104, USA.
William L BerryDepartment of Surgery, University of Oklahoma Health Sciences Center, Oklahoma City, OK 73104, USA.
Lorin E OlsonCardiovascular Biology Research Program, Oklahoma Medical Research Foundation, Oklahoma City, OK 73104, USA; Department of Cell Biology, University of Oklahoma Health Sciences Center, Oklahoma City, OK 73104, USA. Electronic address: lorin-olson@omrf.org.
Oklahoma Medical Research Foundation · USUniversity of Oklahoma Health Sciences Center · US

Funding

Understanding connective tissue development and disease with PDGFR-driven..... P20GM103636 · NIGMS · OKLAHOMA MEDICAL RESEARCH FOUNDATION · PI THOMPSON, LINDA F · 2013 to 2023
$26.9M
TUMOR RESISTANCE MECHANISMS TO ANTI-VEGF THERAPY IN PROSTATE CANCER (Sukyung Woo)P20GM103639 · NIGMS · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI DHANASEKARAN, DANNY N. · 2012 to 2022
$21.3M
Pilot ProjectP30GM114731 · NIGMS · OKLAHOMA MEDICAL RESEARCH FOUNDATION · PI MCEVER, RODGER PAUL · 2016 to 2020
$6.5M
FIBROBLAST DIFFERENTIATION IN WOUND HEALINGR01GM060651 · NIGMS · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI TOMASEK, JAMES J · 2000 to 2017
$3.4M
PDGF-regulated cell fate and dermal fibrosisR01AR070235 · NIAMS · OKLAHOMA MEDICAL RESEARCH FOUNDATION · PI OLSON, LORIN E · 2016 to 2020
$1.9M
PDGF-regulated stem cells and bone diseaseR01AR073828 · NIAMS · OKLAHOMA MEDICAL RESEARCH FOUNDATION · PI OLSON, LORIN E · 2019 to 2023
$1.9M
MECHANISMS DRIVING THE FORMATION OF POST-OPERATIVE PERITONEAL ADHESIONSR35GM142786 · NIGMS · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI BERRY, WILLIAM L · 2021 to 2025
$1.8M
NIAMS NIH HHS R01 AR070235NIAMS NIH HHS R01 AR073828NIGMS NIH HHS P20 GM103636NIGMS NIH HHS P20 GM103639NIGMS NIH HHS P30 GM114731NIGMS NIH HHS R01 GM060651NIGMS NIH HHS R35 GM142786
6 · The paper itself

Abstract

Fibroblasts differentiate into myofibroblasts by acquiring new contractile function. This is important for tissue repair, but it also contributes to organ fibrosis. Platelet-derived growth factor (PDGF) promotes tissue repair and fibrosis, but the relationship between PDGF and myofibroblasts is unclear. Using mice with lineage tracing linked to PDGF receptor α (PDGFRα) gene mutations, we examine cell fates during skin wound healing. Elevated PDGFRα signaling increases proliferation but unexpectedly delays the fibroblast-to-myofibroblast transition, suggesting that PDGFRα must be downregulated for myofibroblast differentiation. In contrast, deletion of PDGFRα decreases proliferation and myofibroblast differentiation by reducing serum response factor (SRF) nuclear localization. Consequences of SRF deletion resemble PDGFRα deletion, but deletion of two SRF coactivators, MRTFA and MRTFB, specifically eliminates myofibroblasts. Our findings suggest a scenario where PDGFRα signaling initially supports proliferation of fibroblast progenitors to expand their number during early wound healing but, later, PDGFRα downregulation facilitates fibroblast differentiation into myofibroblasts.

Indexed as

MyofibroblastsReceptor, Platelet-Derived Growth Factor alphaAnimalsCell DifferentiationFibroblastsFibrosisMicePlatelet-Derived Growth FactorWound HealingPlatelet-Derived Growth FactorReceptor, Platelet-Derived Growth Factor alphaCP: Stem cell researchdermisfibroblastfibrosislineagetracingmyocardin-related transcription factormyofibroblastPdgfrascar tissueSrfwound healing

Identifiers

PMID35977484
PMCPMC9423027
OpenAlexW4292055845

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.