Embryogenesis of the first circulating endothelial cells.
Prior to this study, the earliest appearance of circulating endothelial cells in warm-blooded animals was unknown. Time-lapse imaging of germ-line transformed Tie1-YFP reporter quail embryos combined with the endothelial marker antibody QH1 provides definitive evidence for the existence of circulati...
| Main Authors: | , , , , , , , |
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| Format: | Article |
| Language: | English |
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Public Library of Science (PLoS)
2013-01-01
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| Series: | PLoS ONE |
| Online Access: | http://europepmc.org/articles/PMC3667859?pdf=render |
| _version_ | 1819239355797995520 |
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| author | Cheng Cui Michael B Filla Elizabeth A V Jones Rusty Lansford Tracey Cheuvront Sarah Al-Roubaie Brenda J Rongish Charles D Little |
| author_facet | Cheng Cui Michael B Filla Elizabeth A V Jones Rusty Lansford Tracey Cheuvront Sarah Al-Roubaie Brenda J Rongish Charles D Little |
| author_sort | Cheng Cui |
| collection | DOAJ |
| description | Prior to this study, the earliest appearance of circulating endothelial cells in warm-blooded animals was unknown. Time-lapse imaging of germ-line transformed Tie1-YFP reporter quail embryos combined with the endothelial marker antibody QH1 provides definitive evidence for the existence of circulating endothelial cells - from the very beginning of blood flow. Blood-smear counts of circulating cells from Tie1-YFP embryos showed that up to 30% of blood-borne cells are Tie1 positive; though cells expressing low levels of YFP were also positive for benzidine, a hemoglobin stain, suggesting that these cells were differentiating into erythroblasts. Electroporation-based time-lapse experiments, exclusively targeting the intra-embryonic mesoderm were combined with QH1 immunostaining. The latter antibody marks quail endothelial cells. Together the optical data provide conclusive evidence that endothelial cells can enter blood flow from vessels of the embryo proper, as well as from extra-embryonic areas. When Tie1-YFP positive cells and tissues are transplanted to wild type host embryos, fluorescent cells emigrate from such transplants and join host vessels; subsequently a few YFP cells are shed into circulation. These data establish that entering circulation is a commonplace activity of embryonic vascular endothelial cells. We conclude that in the class of vertebrates most closely related to mammals a normal component of primary vasculogenesis is production of endothelial cells that enter circulation from all vessels, both intra- and extra-embryonic. |
| first_indexed | 2024-12-23T13:50:49Z |
| format | Article |
| id | doaj.art-475caf4660634803ba8793e0f4e31497 |
| institution | Directory Open Access Journal |
| issn | 1932-6203 |
| language | English |
| last_indexed | 2024-12-23T13:50:49Z |
| publishDate | 2013-01-01 |
| publisher | Public Library of Science (PLoS) |
| record_format | Article |
| series | PLoS ONE |
| spelling | doaj.art-475caf4660634803ba8793e0f4e314972022-12-21T17:44:36ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-0185e6084110.1371/journal.pone.0060841Embryogenesis of the first circulating endothelial cells.Cheng CuiMichael B FillaElizabeth A V JonesRusty LansfordTracey CheuvrontSarah Al-RoubaieBrenda J RongishCharles D LittlePrior to this study, the earliest appearance of circulating endothelial cells in warm-blooded animals was unknown. Time-lapse imaging of germ-line transformed Tie1-YFP reporter quail embryos combined with the endothelial marker antibody QH1 provides definitive evidence for the existence of circulating endothelial cells - from the very beginning of blood flow. Blood-smear counts of circulating cells from Tie1-YFP embryos showed that up to 30% of blood-borne cells are Tie1 positive; though cells expressing low levels of YFP were also positive for benzidine, a hemoglobin stain, suggesting that these cells were differentiating into erythroblasts. Electroporation-based time-lapse experiments, exclusively targeting the intra-embryonic mesoderm were combined with QH1 immunostaining. The latter antibody marks quail endothelial cells. Together the optical data provide conclusive evidence that endothelial cells can enter blood flow from vessels of the embryo proper, as well as from extra-embryonic areas. When Tie1-YFP positive cells and tissues are transplanted to wild type host embryos, fluorescent cells emigrate from such transplants and join host vessels; subsequently a few YFP cells are shed into circulation. These data establish that entering circulation is a commonplace activity of embryonic vascular endothelial cells. We conclude that in the class of vertebrates most closely related to mammals a normal component of primary vasculogenesis is production of endothelial cells that enter circulation from all vessels, both intra- and extra-embryonic.http://europepmc.org/articles/PMC3667859?pdf=render |
| spellingShingle | Cheng Cui Michael B Filla Elizabeth A V Jones Rusty Lansford Tracey Cheuvront Sarah Al-Roubaie Brenda J Rongish Charles D Little Embryogenesis of the first circulating endothelial cells. PLoS ONE |
| title | Embryogenesis of the first circulating endothelial cells. |
| title_full | Embryogenesis of the first circulating endothelial cells. |
| title_fullStr | Embryogenesis of the first circulating endothelial cells. |
| title_full_unstemmed | Embryogenesis of the first circulating endothelial cells. |
| title_short | Embryogenesis of the first circulating endothelial cells. |
| title_sort | embryogenesis of the first circulating endothelial cells |
| url | http://europepmc.org/articles/PMC3667859?pdf=render |
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