Evidence map›Paper›PMID 35293863›Full record

ArticleeLife2022

Adult mouse fibroblasts retain organ-specific transcriptomic identity.

Elvira Forte, Mirana Ramialison, Hieu T Nim, Madison Mara, Jacky Y Li, Rachel Cohn, Sandra L Daigle, Sarah Boyd, Edouard G Stanley, Andrew G Elefanty and 4 more

Open access · goldAbstract read
In one paragraph

Article in eLife, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
3.3field-weighted citation impact, top 7% 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

29 citing papers in PubMed, 42 citations in OpenAlex.

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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

14 authors at 4 institutions in 4 countries.

Elvira Forte *The Jackson Laboratory, Bar Harbor, United States.ORCID 0000-0002-5555-9122
Mirana Ramialison *Australian Regenerative Medicine Institute, Monash University, Clayton, Australia.ORCID 0000-0001-6315-4777
Hieu T Nim *Australian Regenerative Medicine Institute, Monash University, Clayton, Australia.
Madison MaraThe Jackson Laboratory, Bar Harbor, United States.
Jacky Y LiMurdoch Children's Research Institute, The Royal Children's Hospital, Parkville, Australia.
Rachel CohnThe Jackson Laboratory, Farmington, United States.
Sandra L DaigleThe Jackson Laboratory, Bar Harbor, United States.
Sarah BoydCentre for Inflammatory Diseases, School of Clinical Sciences at Monash Health, Monash University, Clayton, Australia.
Edouard G StanleyMurdoch Children's Research Institute, The Royal Children's Hospital, Parkville, Australia.
Andrew G ElefantyMurdoch Children's Research Institute, The Royal Children's Hospital, Parkville, Australia.
John Travis HinsonThe Jackson Laboratory, Farmington, United States.
Mauro W CostaThe Jackson Laboratory, Bar Harbor, United States.
Nadia A Rosenthal *The Jackson Laboratory, Bar Harbor, United States.
Milena B Furtado *The Jackson Laboratory, Bar Harbor, United States.ORCID 0000-0003-1387-325X
Jackson Laboratory · USRoyal Children's Hospital · AUAustralian Regenerative Medicine Institute · AUMonash Health · AU

Funding

Shared Resource ManagementP30CA034196 · NCI · JACKSON LABORATORY · PI William Carl Skarnes · 1985 to 2026
$61.9M
Interventions That Retard Mammalian AgingU01AG022308 · NIA · JACKSON LABORATORY · PI Ronny Korstanje · 2003 to 2026
$30.5M
Understanding the role of thyroid hormone signaling during axolotl limb regenerationP20GM104318 · NIGMS · MOUNT DESERT ISLAND BIOLOGICAL LAB · PI DRUMMOND, IAIN A. · 2013 to 2023
$23.0M
NCI NIH HHS P30 CA034196NIA NIH HHS U01 AG022308NIGMS NIH HHS P20 GM104318
6 · The paper itself

Abstract

Organ fibroblasts are essential components of homeostatic and diseased tissues. They participate in sculpting the extracellular matrix, sensing the microenvironment, and communicating with other resident cells. Recent studies have revealed transcriptomic heterogeneity among fibroblasts within and between organs. To dissect the basis of interorgan heterogeneity, we compare the gene expression of murine fibroblasts from different tissues (tail, skin, lung, liver, heart, kidney, and gonads) and show that they display distinct positional and organ-specific transcriptome signatures that reflect their embryonic origins. We demonstrate that expression of genes typically attributed to the surrounding parenchyma by fibroblasts is established in embryonic development and largely maintained in culture, bioengineered tissues and ectopic transplants. Targeted knockdown of key organ-specific transcription factors affects fibroblast functions, in particular genes involved in the modulation of fibrosis and inflammation. In conclusion, our data reveal that adult fibroblasts maintain an embryonic gene expression signature inherited from their organ of origin, thereby increasing our understanding of adult fibroblast heterogeneity. The knowledge of this tissue-specific gene signature may assist in targeting fibrotic diseases in a more precise, organ-specific manner.

Indexed as

FibroblastsTranscriptomeAnimalsFibrosisLungMiceSkincell biologydevelopmental biologyembryonic developmentfibroblastsHox codemouseorgan identityorgan specifictranscriptome

Identifiers

PMID35293863
PMCPMC8959603
OpenAlexW4220845466

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.