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

Author:

Schulz Christian12,Perdiguero Elisa Gomez12,Chorro Laurent12,Szabo-Rogers Heather3,Cagnard Nicolas4,Kierdorf Katrin5,Prinz Marco5,Wu Bishan6,Jacobsen Sten Eirik W.6,Pollard Jeffrey W.7,Frampton Jon8,Liu Karen J.3,Geissmann Frederic12

Affiliation:

1. Centre for Molecular and Cellular Biology of Inflammation (CMCBI), New Hunt’s House, King's College London, Great Maze Pond, London SE1 1UL, UK.

2. Peter Gorer Department of Immunobiology, King's College London, London SE1 9RT, UK.

3. Department of Craniofacial Development, King's College London, London SE1 9RT, UK.

4. Plateforme Bioinformatique INSERM/IRNEM-IFR94, Université Paris Descartes, 149 rue de Sèvres, 75015 Paris, France.

5. Department of Neuropathology, University of Freiburg, and BIOSS Centre for Biological Signalling Studies, University of Freiburg, 79106 Freiburg, Germany.

6. Haematopoietic Stem Cell Biology Laboratory, Weatherall Institute of Molecular Medicine, University of Oxford, John Radcliffe Hospital, Oxford OX3 9DS, UK.

7. Department of Developmental and Molecular Biology, Center for the Study of Reproductive Biology and Women's Health, Albert Einstein College of Medicine, New York, NY 10461, USA.

8. College of Medical and Dental Sciences, University of Birmingham, Edgbaston, Birmingham B15 2TT, UK.

Abstract

Macrophage Development Rewritten Macrophages provide protection against a wide variety of infections and critically shape the inflammatory environment in many tissues. These cells come in many flavors, as determined by differences in gene expression, cell surface phenotype and specific function. Schulz et al. (p. 86 , published online 22 March) investigated whether adult macrophages all share a common developmental origin. Immune cells, including most macrophages, are widely thought to arise from hematopoietic stem cells (HSCs), which require the transcription factor Myb for their development. Analysis of Myb-deficient mice revealed that a population of yolk-sac–derived, tissue-resident macrophages was able to develop and persist in adult mice in the absence of HSCs. Importantly, yolk sac–derived macrophages also contributed substantially to the tissue macrophage pool even when HSCs were present.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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