Evidence map›Paper›PMID 35187598›Full record

ReviewCellular and molecular life sciences : CMLS2022

Multicolor strategies for investigating clonal expansion and tissue plasticity.

L Dumas, S Clavreul, F Michon, K Loulier

Open access · hybridAbstract readReview
In one paragraph

Review in Cellular and molecular life sciences : CMLS, 2022. 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
1.7field-weighted citation impact, top 16% 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, 20 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

4 authors at 1 institution in 1 country.

L Dumas *Institute for Neurosciences of Montpellier (INM), Univ Montpellier, INSERM, Montpellier, France.ORCID https://orcid.org/0000-0001-7500-9067
S Clavreul *Institute for Neurosciences of Montpellier (INM), Univ Montpellier, INSERM, Montpellier, France.ORCID https://orcid.org/0000-0001-5384-8425
F MichonInstitute for Neurosciences of Montpellier (INM), Univ Montpellier, INSERM, Montpellier, France.ORCID https://orcid.org/0000-0003-4305-305X
K LoulierInstitute for Neurosciences of Montpellier (INM), Univ Montpellier, INSERM, Montpellier, France. karine.loulier@inserm.fr.ORCID https://orcid.org/0000-0001-6216-2708
Inserm · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Understanding the generation of complexity in living organisms requires the use of lineage tracing tools at a multicellular scale. In this review, we describe the different multicolor strategies focusing on mouse models expressing several fluorescent reporter proteins, generated by classical (MADM, Brainbow and its multiple derivatives) or acute (StarTrack, CLoNe, MAGIC Markers, iOn, viral vectors) transgenesis. After detailing the multi-reporter genetic strategies that serve as a basis for the establishment of these multicolor mouse models, we briefly mention other animal and cellular models (zebrafish, chicken, drosophila, iPSC) that also rely on these constructs. Then, we highlight practical applications of multicolor mouse models to better understand organogenesis at single progenitor scale (clonal analyses) in the brain and briefly in several other tissues (intestine, skin, vascular, hematopoietic and immune systems). In addition, we detail the critical contribution of multicolor fate mapping strategies in apprehending the fine cellular choreography underlying tissue morphogenesis in several models with a particular focus on brain cytoarchitecture in health and diseases. Finally, we present the latest technological advances in multichannel and in-depth imaging, and automated analyses that enable to better exploit the large amount of data generated from multicolored tissues.

Indexed as

Cell LineageOrganogenesisAnimalsAnimals, Genetically ModifiedCell TrackingClone CellsHumansLuminescent ProteinsOrgan SpecificityLuminescent ProteinsBrainFluorescent reportersLineage tracingMorphogenesisMultichannel imagingTransgenic mouse

Identifiers

PMID35187598
PMCPMC8858928
OpenAlexW4212971126

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.