Comparison of gene expression profiles between human and mouse monocyte subsets

Author:

Ingersoll Molly A.1,Spanbroek Rainer2,Lottaz Claudio3,Gautier Emmanuel L.1,Frankenberger Marion4,Hoffmann Reinhard5,Lang Roland6,Haniffa Muzlifah7,Collin Matthew7,Tacke Frank1,Habenicht Andreas J. R.2,Ziegler-Heitbrock Loems4,Randolph Gwendalyn J.1

Affiliation:

1. Department of Gene and Cell Medicine and Immunology Institute, Mount Sinai School of Medicine, New York, NY;

2. Institute for Vascular Medicine, Friedrich Schiller University of Jena, Jena, Germany;

3. Institute of Functional Genomics, University of Regensburg, Regensburg, Germany;

4. Clinical Cooperation Group “Inflammatory Lung Diseases,” Asklepios-Fachklinik and Helmholtz Zentrum München, German Research Center for Environmental Health, Gauting, Germany;

5. Institute for Medical Microbiology, Immunology und Hygiene, Technische Universität München, München, Germany;

6. Institute of Clinical Microbiology, Immunology and Hygiene, University Hospital Erlangen, Erlangen, Germany; and

7. Institute of Cellular Medicine, Newcastle University, Newcastle upon Tyne, United Kingdom

Abstract

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 γ (PPARγ) 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.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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