Comparison of gene expression profiles between human and mouse monocyte subsets

Molly A. Ingersoll(Icahn School of Medicine at Mount Sinai), Rainer Spanbroek(Friedrich Schiller University Jena), Claudio Lottaz(University of Regensburg), Emmanuel L. Gautier(Icahn School of Medicine at Mount Sinai), Marion Frankenberger(Helmholtz Zentrum München), Reinhard Hoffmann(Institute of Medical Microbiology and Hygiene), Roland Lang(Universitätsklinikum Erlangen), Muzlifah Haniffa(Newcastle University), Matthew Collin(Newcastle University), Frank Tacke(Icahn School of Medicine at Mount Sinai), Andreas J. R. Habenicht(Friedrich Schiller University Jena), Loems Ziegler‐Heitbrock(Helmholtz Zentrum München), Gwendalyn J. Randolph(Icahn School of Medicine at Mount Sinai)
Blood
November 12, 2009
Cited by 709Open Access
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Abstract

Blood of both humans and mice contains 2 main monocyte subsets. Here, we investigated the extent of their similarity using a microarray approach. Approximately 270 genes in humans and 550 genes in mice were differentially expressed between subsets by 2-fold or more. More than 130 of these gene expression differences were conserved between mouse and human monocyte subsets. We confirmed numerous of these differences at the cell surface protein level. Despite overall conservation, some molecules were conversely expressed between the 2 species' subsets, including CD36, CD9, and TREM-1. Other differences included a prominent peroxisome proliferator-activated receptor gamma (PPARgamma) signature in mouse monocytes, which is absent in humans, and strikingly opposed patterns of receptors involved in uptake of apoptotic cells and other phagocytic cargo between human and mouse monocyte subsets. Thus, whereas human and mouse monocyte subsets are far more broadly conserved than currently recognized, important differences between the species deserve consideration when models of human disease are studied in mice.


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