A Lineage of Myeloid Cells Independent of Myb and Hematopoietic Stem Cells

Christian Schulz(King's College London), Elisa Gomez Perdiguero(King's College London), Laurent Chorro(King's College London), Heather L. Szabo‐Rogers(King's College London), Nicolas Cagnard(Délégation Paris 5), Katrin Kierdorf(University of Freiburg), Marco Prinz(University of Freiburg), Bishan Wu(John Radcliffe Hospital), Sten Eirik W. Jacobsen(John Radcliffe Hospital), Jeffrey W. Pollard(Albert Einstein College of Medicine), Jon Frampton(University of Birmingham), Karen Liu(King's College London), Frédéric Geissmann(King's College London)
Science
March 23, 2012
Cited by 2,514

Abstract

Macrophages and dendritic cells (DCs) are key components of cellular immunity and are thought to originate and renew from hematopoietic stem cells (HSCs). However, some macrophages develop in the embryo before the appearance of definitive HSCs. We thus reinvestigated macrophage development. We found that the transcription factor Myb was required for development of HSCs and all CD11b(high) monocytes and macrophages, but was dispensable for yolk sac (YS) macrophages and for the development of YS-derived F4/80(bright) macrophages in several tissues, such as liver Kupffer cells, epidermal Langerhans cells, and microglia--cell populations that all can persist in adult mice independently of HSCs. These results define a lineage of tissue macrophages that derive from the YS and are genetically distinct from HSC progeny.


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