Evidence map›Paper›PMID 27060598›Full record

ArticleGenesis (New York, N.Y. : 2000)2016

Pdgfrb-Cre targets lymphatic endothelial cells of both venous and non-venous origins.

Maria H Ulvmar, Ines Martinez-Corral, Lukas Stanczuk, Taija Mäkinen

Open access · bronzeAbstract read
In one paragraph

Article in Genesis (New York, N.Y. : 2000), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.4field-weighted citation impact, top 10% 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

23 citing papers in PubMed, 34 citations in OpenAlex.

  1. Review
  2. Article
  3. Identification of distinct vascular mural cell populations during zebrafish embryonic development.Developmental dynamics : an official publication of the American Association of Anatomists · 2024
    Article
  4. Article
  5. Article
  6. Review
  7. PDGFRβCell reports · 2022
    Article
  8. Review
  9. Review
  10. Patterns of differentiation of renin lineage cells during nephrogenesis.American journal of physiology. Renal physiology · 2021
    Article
  11. Review
  12. Review
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Cardiac lymphatics in health and disease.Nature reviews. Cardiology · 2019
    Review
  20. 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

4 authors at 1 institution in 1 country.

Maria H UlvmarDepartment of Immunology Genetics and Pathology, Uppsala University, Dag Hammarskjöldsväg 20, 751 85, Uppsala, Sweden.
Ines Martinez-CorralDepartment of Immunology Genetics and Pathology, Uppsala University, Dag Hammarskjöldsväg 20, 751 85, Uppsala, Sweden.
Lukas StanczukDepartment of Immunology Genetics and Pathology, Uppsala University, Dag Hammarskjöldsväg 20, 751 85, Uppsala, Sweden.
Taija MäkinenDepartment of Immunology Genetics and Pathology, Uppsala University, Dag Hammarskjöldsväg 20, 751 85, Uppsala, Sweden.
Uppsala University · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The Pdgfrb-Cre line has been used as a tool to specifically target pericytes and vascular smooth muscle cells. Recent studies showed additional targeting of cardiac and mesenteric lymphatic endothelial cells (LECs) by the Pdgfrb-Cre transgene. In the heart, this was suggested to provide evidence for a previously unknown nonvenous source of LECs originating from yolk sac (YS) hemogenic endothelium (HemEC). Here we show that Pdgfrb-Cre does not, however, target YS HemEC or YS-derived erythro-myeloid progenitors (EMPs). Instead, a high proportion of ECs in embryonic blood vessels of multiple organs, as well as venous-derived LECs were targeted. Assessment of temporal Cre activity using the R26-mTmG double reporter suggested recent occurrence of Pdgfrb-Cre recombination in both blood and lymphatic ECs. It thus cannot be excluded that Pdgfrb-Cre mediated targeting of LECs is due to de novo expression of the Pdgfrb-Cre transgene or their previously established venous endothelial origin. Importantly, Pdgfrb-Cre targeting of LECs does not provide evidence for YS HemEC origin of the lymphatic vasculature. Our results highlight the need for careful interpretation of lineage tracing using constitutive Cre lines that cannot discriminate active from historical expression. The early vascular targeting by the Pdgfrb-Cre also warrants consideration for its use in studies of mural cells. genesis 54:350-358, 2016. © 2016 The Authors. Genesis Published by Wiley Periodicals, Inc.

Indexed as

AnimalsCell LineageEndothelial CellsGene TargetingHeartIntegrasesLymphangiogenesisLymphatic VesselsMice, TransgenicMyocytes, Smooth MuscleReceptor, Platelet-Derived Growth Factor betaVeinsYolk SacCre recombinaseIntegrasesReceptor, Platelet-Derived Growth Factor betalymphangiogenesislymphvasculogenesismural cellvascular development

Identifiers

PMID27060598
PMCPMC5021155
OpenAlexW2335950808

What OpenQuestion holds

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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.