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Prostaglandin E2 promotes embryonic vascular development and maturation in zebrafish
Prostaglandin (PG)-E2 is essential for growth and development of vertebrates. PGE2 binds to G-coupled receptors to regulate embryonic stem cell differentiation and maintains tissue homeostasis. Overproduction of PGE2 by breast tumor cells promotes aggressive breast cancer phenotypes and tumor-associ...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Company of Biologists Ltd
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6504002/ https://www.ncbi.nlm.nih.gov/pubmed/30890523 http://dx.doi.org/10.1242/bio.039768 |
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author | Ugwuagbo, Kingsley Chukwunonso Maiti, Sujit Omar, Ahmed Hunter, Stephanie Nault, Braydon Northam, Caleb Majumder, Mousumi |
author_facet | Ugwuagbo, Kingsley Chukwunonso Maiti, Sujit Omar, Ahmed Hunter, Stephanie Nault, Braydon Northam, Caleb Majumder, Mousumi |
author_sort | Ugwuagbo, Kingsley Chukwunonso |
collection | PubMed |
description | Prostaglandin (PG)-E2 is essential for growth and development of vertebrates. PGE2 binds to G-coupled receptors to regulate embryonic stem cell differentiation and maintains tissue homeostasis. Overproduction of PGE2 by breast tumor cells promotes aggressive breast cancer phenotypes and tumor-associated lymphangiogenesis. In this study, we investigated novel roles of PGE2 in early embryonic vascular development and maturation with the microinjection of PGE2 in fertilized zebrafish (Danio rerio) eggs. We injected Texas Red dextran to trace vascular development. Embryos injected with the solvent of PGE2 served as vehicle. Distinct developmental changes were noted from 28–96 h post fertilization (hpf), showing an increase in embryonic tail flicks, pigmentation, growth, hatching and larval movement post-hatching in the PGE2-injected group compared to the vehicle. We recorded a significant increase in trunk vascular fluorescence and maturation of vascular anatomy, embryo heartbeat and blood vessel formation in the PGE2 injected group. At 96 hpf, all larvae were euthanized to measure vascular marker mRNA expression. We observed a significant increase in the expression of stem cell markers efnb2a, ephb4a, angiogenesis markers vegfa, kdrl, etv2 and lymphangiogenesis marker prox1 in the PGE2-group compared to the vehicle. This study shows the novel roles of PGE2 in promoting embryonic vascular maturation and angiogenesis in zebrafish. This article has an associated First Person interview with the first author of the paper. |
format | Online Article Text |
id | pubmed-6504002 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | The Company of Biologists Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-65040022019-05-08 Prostaglandin E2 promotes embryonic vascular development and maturation in zebrafish Ugwuagbo, Kingsley Chukwunonso Maiti, Sujit Omar, Ahmed Hunter, Stephanie Nault, Braydon Northam, Caleb Majumder, Mousumi Biol Open Research Article Prostaglandin (PG)-E2 is essential for growth and development of vertebrates. PGE2 binds to G-coupled receptors to regulate embryonic stem cell differentiation and maintains tissue homeostasis. Overproduction of PGE2 by breast tumor cells promotes aggressive breast cancer phenotypes and tumor-associated lymphangiogenesis. In this study, we investigated novel roles of PGE2 in early embryonic vascular development and maturation with the microinjection of PGE2 in fertilized zebrafish (Danio rerio) eggs. We injected Texas Red dextran to trace vascular development. Embryos injected with the solvent of PGE2 served as vehicle. Distinct developmental changes were noted from 28–96 h post fertilization (hpf), showing an increase in embryonic tail flicks, pigmentation, growth, hatching and larval movement post-hatching in the PGE2-injected group compared to the vehicle. We recorded a significant increase in trunk vascular fluorescence and maturation of vascular anatomy, embryo heartbeat and blood vessel formation in the PGE2 injected group. At 96 hpf, all larvae were euthanized to measure vascular marker mRNA expression. We observed a significant increase in the expression of stem cell markers efnb2a, ephb4a, angiogenesis markers vegfa, kdrl, etv2 and lymphangiogenesis marker prox1 in the PGE2-group compared to the vehicle. This study shows the novel roles of PGE2 in promoting embryonic vascular maturation and angiogenesis in zebrafish. This article has an associated First Person interview with the first author of the paper. The Company of Biologists Ltd 2019-04-15 /pmc/articles/PMC6504002/ /pubmed/30890523 http://dx.doi.org/10.1242/bio.039768 Text en © 2019. Published by The Company of Biologists Ltd http://creativecommons.org/licenses/by/4.0This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed. |
spellingShingle | Research Article Ugwuagbo, Kingsley Chukwunonso Maiti, Sujit Omar, Ahmed Hunter, Stephanie Nault, Braydon Northam, Caleb Majumder, Mousumi Prostaglandin E2 promotes embryonic vascular development and maturation in zebrafish |
title | Prostaglandin E2 promotes embryonic vascular development and maturation in zebrafish |
title_full | Prostaglandin E2 promotes embryonic vascular development and maturation in zebrafish |
title_fullStr | Prostaglandin E2 promotes embryonic vascular development and maturation in zebrafish |
title_full_unstemmed | Prostaglandin E2 promotes embryonic vascular development and maturation in zebrafish |
title_short | Prostaglandin E2 promotes embryonic vascular development and maturation in zebrafish |
title_sort | prostaglandin e2 promotes embryonic vascular development and maturation in zebrafish |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6504002/ https://www.ncbi.nlm.nih.gov/pubmed/30890523 http://dx.doi.org/10.1242/bio.039768 |
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