Summary of ssbd-repos-000135

SSBD:database
URL

Name
ssbd-repos-000135 (135-Maruyama-LymVesselImmuno)
URL
DOI
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Title
Immunostaining images of Prox1, PECAM or VEGER3 expression in mouse embryo different developmental stage
Description
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Submited Date
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Release Date
2019-11-20
Updated Date
-
License
Funding information
-
File formats
Data size
58.9 MB

Organism
M. musculus
Strain
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Cell Line
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Genes
Prox1
Proteins
PECAM, VEGFR3

GO Molecular Function (MF)
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GO Biological Process (BP)
lymphatic vascular process in circulatory system, lymphatic endothelial cell differentiation
GO Cellular Component (CC)
NA
Study Type
-
Imaging Methods
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Method Summary
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Related paper(s)

Kazuaki Maruyama, Sachiko Miyagawa-Tomita, Kaoru Mizukami, Fumio Matsuzaki, Hiroki Kurihara (2019) Isl1-expressing non-venous cell lineage contributes to cardiac lymphatic vessel development., Developmental biology, Volume 452, Number 2, pp. 134-143

Published in 2019 Aug 15 (Electronic publication in May 18, 2019, midnight )

(Abstract) The origin of the mammalian lymphatic vasculature has been studied for more than a century; however, details regarding organ-specific lymphatic development remain unknown. A recent study reported that cardiac lymphatic endothelial cells (LECs) stem from venous and non-venous origins in mice. Here, we identified Isl1-expressing progenitors as a potential non-venous origin of cardiac LECs. Genetic lineage tracing with Isl1-Cre reporter mice suggested a possible contribution from the Isl1-expressing pharyngeal mesoderm constituting the second heart field to lymphatic vessels around the cardiac outflow tract as well as to those in the facial skin and the lymph sac. Isl1(+) lineage-specific deletion of Prox1 resulted in disrupted LYVE1(+) vessel structures, indicating a Prox1-dependent mechanism in this contribution. Tracing back to earlier embryonic stages revealed the presence of VEGFR3(+) and/or Prox1(+) cells that overlapped with the Isl1(+) pharyngeal core mesoderm. These data may provide insights into the developmental basis of heart diseases involving lymphatic vasculature and improve our understanding of organ-based lymphangiogenesis.
(MeSH Terms)

Contact(s)
Hiroki Kurihara
Organization(s)
The University of Tokyo , Graduate School of Medicine , Department of Physiological Chemistry and Metabolism
Image Data Contributors
Quantitative Data Contributors

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