Evidence map›Paper›PMID 27342817›Full record

ReviewDifferentiation; research in biological diversity2016

Genetic tools for identifying and manipulating fibroblasts in the mouse.

Jessica M Swonger, Jocelyn S Liu, Malina J Ivey, Michelle D Tallquist

Abstract readReview
In one paragraph

Review in Differentiation; research in biological diversity, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 60 papers.

0numbers the graph read from it
0cells of the map it votes in
60citing 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

60 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Fibroblast orchestration of inflammaging via NF-kB activation.bioRxiv : the preprint server for biology · 2025
    Article
  7. Article
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  15. Article
  16. Review
  17. 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

4 authors.

Jessica M SwongerDepartments of Medicine and Cell and Molecular Biology, John A. Burns School of Medicine, University of Hawaii, Honolulu, HI 96813, USA.
Jocelyn S LiuDepartments of Medicine and Cell and Molecular Biology, John A. Burns School of Medicine, University of Hawaii, Honolulu, HI 96813, USA.
Malina J IveyDepartments of Medicine and Cell and Molecular Biology, John A. Burns School of Medicine, University of Hawaii, Honolulu, HI 96813, USA.
Michelle D TallquistDepartments of Medicine and Cell and Molecular Biology, John A. Burns School of Medicine, University of Hawaii, Honolulu, HI 96813, USA. Electronic address: mseidel@hawaii.edu.

Funding

Microenvironmental control of progenitors in organ dysfunction and repairU01HL100401 · NHLBI · UT SOUTHWESTERN MEDICAL CENTER · PI OLSON, ERIC N, SCHNEIDER, JAY W · 2009 to 2015
$8.3M
Pilot Project ProgramP30GM103341 · NIGMS · UNIVERSITY OF HAWAII AT MANOA · PI SHOHET, RALPH V. · 2012 to 2016
$5.5M
Training in Cardiovascular Research at the University of HawaiiT32HL115505 · NHLBI · UNIVERSITY OF HAWAII AT MANOA · PI Michelle D Tallquist · 2012 to 2026
$3.8M
PDGF Receptor Signaling in Mammalian DevelopmentR01HL074257 · NHLBI · UT SOUTHWESTERN MEDICAL CENTER · PI TALLQUIST, MICHELLE D · 2003 to 2014
$3.7M
Role of Tcf21 in Cardiac Fibroblast FunctionF31HL128048 · NHLBI · UNIVERSITY OF HAWAII AT MANOA · PI SWONGER, JESSICA · 2015 to 2016
$76k
The role of PDGF Receptor Signaling in Cardiac FibroblastsF31HL126512 · NHLBI · UNIVERSITY OF HAWAII AT MANOA · PI IVEY, MALINA JAN · 2015 to 2016
$64k
NHLBI NIH HHS F31 HL126512NHLBI NIH HHS F31 HL128048NHLBI NIH HHS R01 HL074257NHLBI NIH HHS T32 HL115505NHLBI NIH HHS U01 HL100401NIGMS NIH HHS P30 GM103341
6 · The paper itself

Abstract

The use of mouse genetic tools to track and manipulate fibroblasts has provided invaluable in vivo information regarding the activities of these cells. Recently, many new mouse strains have been described for the specific purpose of studying fibroblast behavior. Colorimetric reporter mice and lines expressing Cre are available for the study of fibroblasts in the organs prone to fibrosis, including heart, kidney, liver, lung, and skeletal muscle. In this review we summarize the current state of the models that have been used to define tissue resident fibroblast populations. While these complex genetic reagents provide unique insights into the process of fibrosis, they also require a thorough understanding of the caveats and limitations. Here, we discuss the specificity and efficiency of the available genetic models and briefly describe how they have been used to document the mechanisms of fibrosis.

Indexed as

Pathology, MolecularAnimalsFibroblastsFibrosisHumansIntegrasesLungMice, TransgenicIntegrasesCre recombinaseFibroblastsFibrosisPericytes

Identifiers

PMID27342817
PMCPMC5079827

What OpenQuestion holds

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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.