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Spatiotemporal dynamics and heterogeneity of renal lymphatics in mammalian development and cystic kidney disease
Heterogeneity of lymphatic vessels during embryogenesis is critical for organ-specific lymphatic function. Little is known about lymphatics in the developing kidney, despite their established roles in pathology of the mature organ. We performed three-dimensional imaging to characterize lymphatic ves...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6948954/ https://www.ncbi.nlm.nih.gov/pubmed/31808745 http://dx.doi.org/10.7554/eLife.48183 |
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author | Jafree, Daniyal J Moulding, Dale Kolatsi-Joannou, Maria Perretta Tejedor, Nuria Price, Karen L Milmoe, Natalie J Walsh, Claire L Correra, Rosa Maria Winyard, Paul JD Harris, Peter C Ruhrberg, Christiana Walker-Samuel, Simon Riley, Paul R Woolf, Adrian S Scambler, Peter J Long, David A |
author_facet | Jafree, Daniyal J Moulding, Dale Kolatsi-Joannou, Maria Perretta Tejedor, Nuria Price, Karen L Milmoe, Natalie J Walsh, Claire L Correra, Rosa Maria Winyard, Paul JD Harris, Peter C Ruhrberg, Christiana Walker-Samuel, Simon Riley, Paul R Woolf, Adrian S Scambler, Peter J Long, David A |
author_sort | Jafree, Daniyal J |
collection | PubMed |
description | Heterogeneity of lymphatic vessels during embryogenesis is critical for organ-specific lymphatic function. Little is known about lymphatics in the developing kidney, despite their established roles in pathology of the mature organ. We performed three-dimensional imaging to characterize lymphatic vessel formation in the mammalian embryonic kidney at single-cell resolution. In mouse, we visually and quantitatively assessed the development of kidney lymphatic vessels, remodeling from a ring-like anastomosis under the nascent renal pelvis; a site of VEGF-C expression, to form a patent vascular plexus. We identified a heterogenous population of lymphatic endothelial cell clusters in mouse and human embryonic kidneys. Exogenous VEGF-C expanded the lymphatic population in explanted mouse embryonic kidneys. Finally, we characterized complex kidney lymphatic abnormalities in a genetic mouse model of polycystic kidney disease. Our study provides novel insights into the development of kidney lymphatic vasculature; a system which likely has fundamental roles in renal development, physiology and disease. |
format | Online Article Text |
id | pubmed-6948954 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-69489542020-01-09 Spatiotemporal dynamics and heterogeneity of renal lymphatics in mammalian development and cystic kidney disease Jafree, Daniyal J Moulding, Dale Kolatsi-Joannou, Maria Perretta Tejedor, Nuria Price, Karen L Milmoe, Natalie J Walsh, Claire L Correra, Rosa Maria Winyard, Paul JD Harris, Peter C Ruhrberg, Christiana Walker-Samuel, Simon Riley, Paul R Woolf, Adrian S Scambler, Peter J Long, David A eLife Developmental Biology Heterogeneity of lymphatic vessels during embryogenesis is critical for organ-specific lymphatic function. Little is known about lymphatics in the developing kidney, despite their established roles in pathology of the mature organ. We performed three-dimensional imaging to characterize lymphatic vessel formation in the mammalian embryonic kidney at single-cell resolution. In mouse, we visually and quantitatively assessed the development of kidney lymphatic vessels, remodeling from a ring-like anastomosis under the nascent renal pelvis; a site of VEGF-C expression, to form a patent vascular plexus. We identified a heterogenous population of lymphatic endothelial cell clusters in mouse and human embryonic kidneys. Exogenous VEGF-C expanded the lymphatic population in explanted mouse embryonic kidneys. Finally, we characterized complex kidney lymphatic abnormalities in a genetic mouse model of polycystic kidney disease. Our study provides novel insights into the development of kidney lymphatic vasculature; a system which likely has fundamental roles in renal development, physiology and disease. eLife Sciences Publications, Ltd 2019-12-06 /pmc/articles/PMC6948954/ /pubmed/31808745 http://dx.doi.org/10.7554/eLife.48183 Text en © 2019, Jafree et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Developmental Biology Jafree, Daniyal J Moulding, Dale Kolatsi-Joannou, Maria Perretta Tejedor, Nuria Price, Karen L Milmoe, Natalie J Walsh, Claire L Correra, Rosa Maria Winyard, Paul JD Harris, Peter C Ruhrberg, Christiana Walker-Samuel, Simon Riley, Paul R Woolf, Adrian S Scambler, Peter J Long, David A Spatiotemporal dynamics and heterogeneity of renal lymphatics in mammalian development and cystic kidney disease |
title | Spatiotemporal dynamics and heterogeneity of renal lymphatics in mammalian development and cystic kidney disease |
title_full | Spatiotemporal dynamics and heterogeneity of renal lymphatics in mammalian development and cystic kidney disease |
title_fullStr | Spatiotemporal dynamics and heterogeneity of renal lymphatics in mammalian development and cystic kidney disease |
title_full_unstemmed | Spatiotemporal dynamics and heterogeneity of renal lymphatics in mammalian development and cystic kidney disease |
title_short | Spatiotemporal dynamics and heterogeneity of renal lymphatics in mammalian development and cystic kidney disease |
title_sort | spatiotemporal dynamics and heterogeneity of renal lymphatics in mammalian development and cystic kidney disease |
topic | Developmental Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6948954/ https://www.ncbi.nlm.nih.gov/pubmed/31808745 http://dx.doi.org/10.7554/eLife.48183 |
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