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Yolk sac macrophage progenitors traffic to the embryo during defined stages of development

Tissue macrophages in many adult organs originate from yolk sac (YS) progenitors, which invade the developing embryo and persist by means of local self-renewal. However, the route and characteristics of YS macrophage trafficking during embryogenesis are incompletely understood. Here we show the earl...

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Autores principales: Stremmel, C., Schuchert, R., Wagner, F., Thaler, R., Weinberger, T., Pick, R., Mass, E., Ishikawa-Ankerhold, H. C., Margraf, A., Hutter, S., Vagnozzi, R., Klapproth, S., Frampton, J., Yona, S., Scheiermann, C., Molkentin, J. D., Jeschke, U., Moser, M., Sperandio, M., Massberg, S., Geissmann, F., Schulz, C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5758709/
https://www.ncbi.nlm.nih.gov/pubmed/29311541
http://dx.doi.org/10.1038/s41467-017-02492-2
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author Stremmel, C.
Schuchert, R.
Wagner, F.
Thaler, R.
Weinberger, T.
Pick, R.
Mass, E.
Ishikawa-Ankerhold, H. C.
Margraf, A.
Hutter, S.
Vagnozzi, R.
Klapproth, S.
Frampton, J.
Yona, S.
Scheiermann, C.
Molkentin, J. D.
Jeschke, U.
Moser, M.
Sperandio, M.
Massberg, S.
Geissmann, F.
Schulz, C.
author_facet Stremmel, C.
Schuchert, R.
Wagner, F.
Thaler, R.
Weinberger, T.
Pick, R.
Mass, E.
Ishikawa-Ankerhold, H. C.
Margraf, A.
Hutter, S.
Vagnozzi, R.
Klapproth, S.
Frampton, J.
Yona, S.
Scheiermann, C.
Molkentin, J. D.
Jeschke, U.
Moser, M.
Sperandio, M.
Massberg, S.
Geissmann, F.
Schulz, C.
author_sort Stremmel, C.
collection PubMed
description Tissue macrophages in many adult organs originate from yolk sac (YS) progenitors, which invade the developing embryo and persist by means of local self-renewal. However, the route and characteristics of YS macrophage trafficking during embryogenesis are incompletely understood. Here we show the early migration dynamics of YS-derived macrophage progenitors in vivo using fate mapping and intravital microscopy. From embryonic day 8.5 (E8.5) CX(3)CR1+ pre-macrophages are present in the mouse YS where they rapidly proliferate and gain access to the bloodstream to migrate towards the embryo. Trafficking of pre-macrophages and their progenitors from the YS to tissues peaks around E10.5, dramatically decreases towards E12.5 and is no longer evident from E14.5 onwards. Thus, YS progenitors use the vascular system during a restricted time window of embryogenesis to invade the growing fetus. These findings close an important gap in our understanding of the development of the innate immune system.
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spelling pubmed-57587092018-01-12 Yolk sac macrophage progenitors traffic to the embryo during defined stages of development Stremmel, C. Schuchert, R. Wagner, F. Thaler, R. Weinberger, T. Pick, R. Mass, E. Ishikawa-Ankerhold, H. C. Margraf, A. Hutter, S. Vagnozzi, R. Klapproth, S. Frampton, J. Yona, S. Scheiermann, C. Molkentin, J. D. Jeschke, U. Moser, M. Sperandio, M. Massberg, S. Geissmann, F. Schulz, C. Nat Commun Article Tissue macrophages in many adult organs originate from yolk sac (YS) progenitors, which invade the developing embryo and persist by means of local self-renewal. However, the route and characteristics of YS macrophage trafficking during embryogenesis are incompletely understood. Here we show the early migration dynamics of YS-derived macrophage progenitors in vivo using fate mapping and intravital microscopy. From embryonic day 8.5 (E8.5) CX(3)CR1+ pre-macrophages are present in the mouse YS where they rapidly proliferate and gain access to the bloodstream to migrate towards the embryo. Trafficking of pre-macrophages and their progenitors from the YS to tissues peaks around E10.5, dramatically decreases towards E12.5 and is no longer evident from E14.5 onwards. Thus, YS progenitors use the vascular system during a restricted time window of embryogenesis to invade the growing fetus. These findings close an important gap in our understanding of the development of the innate immune system. Nature Publishing Group UK 2018-01-08 /pmc/articles/PMC5758709/ /pubmed/29311541 http://dx.doi.org/10.1038/s41467-017-02492-2 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Stremmel, C.
Schuchert, R.
Wagner, F.
Thaler, R.
Weinberger, T.
Pick, R.
Mass, E.
Ishikawa-Ankerhold, H. C.
Margraf, A.
Hutter, S.
Vagnozzi, R.
Klapproth, S.
Frampton, J.
Yona, S.
Scheiermann, C.
Molkentin, J. D.
Jeschke, U.
Moser, M.
Sperandio, M.
Massberg, S.
Geissmann, F.
Schulz, C.
Yolk sac macrophage progenitors traffic to the embryo during defined stages of development
title Yolk sac macrophage progenitors traffic to the embryo during defined stages of development
title_full Yolk sac macrophage progenitors traffic to the embryo during defined stages of development
title_fullStr Yolk sac macrophage progenitors traffic to the embryo during defined stages of development
title_full_unstemmed Yolk sac macrophage progenitors traffic to the embryo during defined stages of development
title_short Yolk sac macrophage progenitors traffic to the embryo during defined stages of development
title_sort yolk sac macrophage progenitors traffic to the embryo during defined stages of development
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5758709/
https://www.ncbi.nlm.nih.gov/pubmed/29311541
http://dx.doi.org/10.1038/s41467-017-02492-2
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