Evidence map›Paper›PMID 32764293›Full record

ArticleInternational journal of molecular sciences2020

Attenuation of Flightless I Increases Human Pericyte Proliferation, Migration and Angiogenic Functions and Improves Healing in Murine Diabetic Wounds.

Hannah M Thomas, Parinaz Ahangar, Benjamin R Hofma, Xanthe L Strudwick, Robert Fitridge, Stuart J Mills, Allison J Cowin

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.2field-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

10 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Wound Healing from an Actin Cytoskeletal Perspective.Cold Spring Harbor perspectives in biology · 2022
    Review
  7. Article
  8. Article
  9. Article
  10. Review
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

7 authors at 2 institutions in 1 country.

Hannah M ThomasFuture Industries Institute, University of South Australia, Adelaide 5000, Australia.
Parinaz AhangarFuture Industries Institute, University of South Australia, Adelaide 5000, Australia.ORCID 0000-0002-0060-3501
Benjamin R HofmaFuture Industries Institute, University of South Australia, Adelaide 5000, Australia.
Xanthe L StrudwickFuture Industries Institute, University of South Australia, Adelaide 5000, Australia.ORCID 0000-0002-8557-3857
Robert FitridgeFaculty of Health and Medical Sciences, University of Adelaide, Adelaide 5000, Australia.
Stuart J MillsFuture Industries Institute, University of South Australia, Adelaide 5000, Australia.ORCID 0000-0002-2462-7081
Allison J CowinFuture Industries Institute, University of South Australia, Adelaide 5000, Australia.ORCID 0000-0003-2885-2080
University of South Australia · AUThe University of Adelaide · AU

Funding

Australian Commonwealth Government ScholarshipCell Therapy Manufacturing Cooperative Research Centre 2-11National Health and Medical Research Council GNT#1002009Playford Trust Scholarship
6 · The paper itself

Abstract

Pericytes are peri-vascular mural cells which have an important role in the homeostatic regulation of inflammatory and angiogenic processes. Flightless I (Flii) is a cytoskeletal protein involved in regulating cellular functions, but its involvement in pericyte activities during wound healing is unknown. Exacerbated inflammation and reduced angiogenesis are hallmarks of impaired diabetic healing responses, and strategies aimed at regulating these processes are vital for improving healing outcomes. To determine the effect of altering Flii expression on pericyte function, in vitro and in vivo studies were performed to assess the effect on healing, inflammation and angiogenesis in diabetic wounds. Here, we demonstrated that human diabetic wounds display upregulated expression of the Flii protein in conjunction with a depletion in the number of platelet derived growth factor receptor β (PDGFRβ) +/ neural glial antigen 2 (NG2) + pericytes present in the dermis. Human pericytes were found to be positive for Flii and attenuating its expression in vitro through siRNA knockdown led to enhanced proliferation, migration and angiogenic functions. Genetic knockdown of

Indexed as

AnimalsCell ProliferationCytoskeletal ProteinsDiabetes ComplicationsDiabetes MellitusDiabetic FootHumansInflammationMiceMicrofilament ProteinsPericytesTrans-ActivatorsWound HealingCytoskeletal ProteinsFLII protein, humanFlII protein, mouseMicrofilament ProteinsTrans-Activatorsangiogenesisdiabetesflightless Iinflammationpericyteswound healing

Identifiers

PMID32764293
PMCPMC7460558
OpenAlexW3047342089

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.