Paraxial Mesoderm Is the Major Source of Lymphatic Endothelium
Developmental Cell, ISSN: 1534-5807, Vol: 50, Issue: 2, Page: 247-255.e3
2019
- 91Citations
- 106Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Metrics Details
- Citations91
- Citation Indexes90
- 90
- CrossRef56
- Policy Citations1
- Policy Citation1
- Captures106
- Readers106
- 106
Article Description
Endothelial cells (ECs), which line blood and lymphatic vessels, are generally described to come from the lateral plate mesoderm despite experimental evidence for a broader source of origin, including the paraxial mesoderm (PXM). Current dogma suggests that following specification from mesoderm, local environmental cues establish the distinct molecular and functional characteristics of ECs in different vascular beds. Here we present evidence to challenge this view, showing that lymphatic EC fate is imprinted during transition through the PXM lineage. We show that PXM-derived cells form the lymphatic endothelium of multiple organs and tissues, with a more restricted contribution to blood vessel endothelium. By deleting Prox1 specifically in PXM-derived cells, we show that this lineage is indispensable for lymphatic vessel development. Collectively, our data establish lineage history as a critical determinant of EC specialization, a finding with broad implications for our understanding of vascular development and heterogeneity.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S1534580719303314; http://dx.doi.org/10.1016/j.devcel.2019.04.034; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85069005779&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/31130354; https://linkinghub.elsevier.com/retrieve/pii/S1534580719303314; https://dx.doi.org/10.1016/j.devcel.2019.04.034; https://www.cell.com/developmental-cell/fulltext/S1534-5807(19)30331-4?dgcid=raven_jbs_etoc_email#.XTXtmB-vBAo.twitter; http://www.cell.com/article/S1534580719303314/abstract; http://www.cell.com/article/S1534580719303314/fulltext; http://www.cell.com/article/S1534580719303314/pdf; https://www.cell.com/developmental-cell/abstract/S1534-5807(19)30331-4; https://www.cell.com/developmental-cell/fulltext/S1534-5807(19)30331-4?rss=yes#.XOeX6mkK1Uw.twitter; https://www.cell.com/developmental-cell/fulltext/S1534-5807(19)30331-4; https://www.cell.com/developmental-cell/fulltext/S1534-5807(19)30331-4?rss=yes#.YnzYcbt_asN.twitter; https://www.cell.com/developmental-cell/fulltext/S1534-5807(19)30331-4?rss=yes#.XOcROTb74jM.twitter; https://www.cell.com/developmental-cell/fulltext/S1534-5807(19)30331-4?rss=yes
Elsevier BV
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