Adult Langerhans cells derive predominantly from embryonic fetal liver monocytes with a minor contribution of yolk sac–derived macrophages

Guillaume Hoeffel(Agency for Science, Technology and Research), Yilin Wang(Agency for Science, Technology and Research), Melanie Greter(Icahn School of Medicine at Mount Sinai), Peter See(Agency for Science, Technology and Research), Pearline Teo(Agency for Science, Technology and Research), Benoît Malleret(Agency for Science, Technology and Research), Marylène Leboeuf(Icahn School of Medicine at Mount Sinai), Donovan Low(Agency for Science, Technology and Research), Guillaume Oller(Agency for Science, Technology and Research), Francisca F. Almeida(Agency for Science, Technology and Research), Sharon H.Y. Choy(Agency for Science, Technology and Research), Marcos Grisotto(Universidade Ceuma), Laurent Rénia(Agency for Science, Technology and Research), Simon J. Conway(Indiana University School of Medicine), E. Richard Stanley(Albert Einstein College of Medicine), Jerry Kok Yen Chan(National University of Singapore), Lai Guan Ng(Agency for Science, Technology and Research), Igor M. Samokhvalov(RIKEN), Miriam Mérad(Icahn School of Medicine at Mount Sinai), Florent Ginhoux(Agency for Science, Technology and Research)
The Journal of Experimental Medicine
May 7, 2012
Cited by 736Open Access
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Abstract

Langerhans cells (LCs) are the dendritic cells (DCs) of the epidermis, forming one of the first hematopoietic lines of defense against skin pathogens. In contrast to other DCs, LCs arise from hematopoietic precursors that seed the skin before birth. However, the origin of these embryonic precursors remains unclear. Using in vivo lineage tracing, we identify a first wave of yolk sac (YS)–derived primitive myeloid progenitors that seed the skin before the onset of fetal liver hematopoiesis. YS progenitors migrate to the embryo proper, including the prospective skin, where they give rise to LC precursors, and the brain rudiment, where they give rise to microglial cells. However, in contrast to microglia, which remain of YS origin throughout life, YS-derived LC precursors are largely replaced by fetal liver monocytes during late embryogenesis. Consequently, adult LCs derive predominantly from fetal liver monocyte-derived cells with a minor contribution of YS-derived cells. Altogether, we establish that adult LCs have a dual origin, bridging early embryonic and late fetal myeloid development.


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