Three pathways to mature macrophages in the early mouse yolk sac

Author:

Bertrand Julien Y.1,Jalil Abdelali1,Klaine Michèle1,Jung Steffen1,Cumano Ana1,Godin Isabelle1

Affiliation:

1. From Institut National de la Santé et de la Recherche Médicale (INSERM) U668, Unité de Développement des Lymphocytes, Institut Pasteur, Paris, France; Service Commun de Microscopie Confocale and INSERM U362, Institut Gustave Roussy, Villejuif, France; and Department of Immunology, Weizmann Institute for Science, Rehovot, Israel.

Abstract

AbstractThe existence of macrophages (Mφ) of yolk-sac (YS) origin has been reported in all vertebrate models. However, the nature of their precursors and pathways of differentiation have not been elucidated. Phenotypic and differentiation potential analyses of YS at 7.5 to 10 postcoital days (dpc), performed in CX3CR1GFP embryos, allowed us to discern 3 independent Mφ populations. A first transient wave consisted of mature, maternal-derived Mφpresent as early as 7.5 to 8 dpc. A second wave of committed Mφ precursors arose at 8 dpc (2-4 somite stage) and was followed by a third wave of erythromyeloid precursors (4-6 somite stage). Both types of precursors displayed similar phenotypes and gave rise to CX3CR1/green fluorescent protein (GFP)–positive Mφ, but differed by their differentiation potential, at the clonal level. The combined data of phenotypic, gene-expression, and in situ analyses allowed us to conclude that the previously named “primitive Mφ” corresponded to a mixture of the first transient wave and committed Mφ precursors. Both YS-derived precursors followed a developmental pathway common to adult Mφ and could be qualified as definitive.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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