Evidence map›Paper›PMID 18430230›Full record

ArticleBMC developmental biology2008

Proliferating mesodermal cells in murine embryos exhibiting macrophage and lymphendothelial characteristics.

Kerstin Buttler, Taichi Ezaki, Jörg Wilting

Open access · hybridAbstract read
In one paragraph

Article in BMC developmental biology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

17 citing papers in PubMed, 43 citations in OpenAlex.

  1. Review
  2. Absence of lymphatic vessels in term placenta.BMC pregnancy and childbirth · 2020
    Article
  3. Review
  4. Host immune cellular reactions in corneal neovascularization.International journal of ophthalmology · 2016
    Review
  5. Review
  6. Review
  7. Article
  8. Lymphatic vessels and tertiary lymphoid organs.The Journal of clinical investigation · 2014
    Review
  9. Article
  10. Article
  11. Article
  12. Myeloid cells and lymphangiogenesis.Cold Spring Harbor perspectives in medicine · 2012
    Review
  13. Article
  14. Formation of cardiovascular tubes in invertebrates and vertebrates.Cellular and molecular life sciences : CMLS · 2010
    Review
  15. Article
  16. Lymphatic development.Birth defects research. Part C, Embryo today : reviews · 2009
    Review
  17. 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

3 authors at 2 institutions in 2 countries.

Kerstin ButtlerCentre of Anatomy, Department of Anatomy and Cell Biology, University Medicine Goettingen, Goettingen, Germany. buttler.kerstin@med.uni-goettingen.de
Taichi Ezaki
Jörg Wilting
University of Göttingen · DETokyo Women's Medical University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe data on the embryonic origin of lymphatic endothelial cells (LECs) from either deep embryonic veins or mesenchymal (or circulating) lymphangioblasts presently available remain inconsistent. In various vertebrates, markers for LECs are first expressed in specific segments of embryonic veins arguing for a venous origin of lymph vessels. Very recently, studies on the mouse have strongly supported this view. However, in the chick, we have observed a dual origin of LECs from veins and from mesodermal lymphangioblasts. Additionally, in murine embryos we have detected mesenchymal cells that co-express LEC markers and the pan-leukocyte marker CD45. Here, we have characterized the mesoderm of murine embryos with LEC markers Prox1, Lyve-1 and LA102 in combination with macrophage markers CD11b and F4/80.

resultsWe observed cells co-expressing both types of markers (e.g. Prox1 - Lyve-1 - F4/80 triple-positive) located in the mesoderm, immediately adjacent to, and within lymph vessels. Our proliferation studies with Ki-67 antibodies showed high proliferative capacities of both the Lyve-1-positive LECs of lymph sacs/lymphatic sprouts and the Lyve-1-positive mesenchymal cells.

conclusionOur data argue for a dual origin of LECs in the mouse, although the primary source of embryonic LECs may reside in specific embryonic veins and mesenchymal lymphangioblasts integrated secondarily into lymph vessels. The impact of a dual source of LECs for ontogenetic, phylogenetic and pathological lymphangiogenesis is discussed.

Indexed as

Cell DifferentiationCell ProliferationAnimalsEmbryo, MammalianEmbryonic Stem CellsEndothelium, LymphaticFluorescent Antibody TechniqueImmunohistochemistryMacrophagesMesodermMiceMice, Inbred C57BL

Identifiers

PMID18430230
PMCPMC2375885
OpenAlexW2103705636

What OpenQuestion holds

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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.