Identification of Splenic Reservoir Monocytes and Their Deployment to Inflammatory Sites

Author:

Swirski Filip K.1,Nahrendorf Matthias1,Etzrodt Martin12,Wildgruber Moritz1,Cortez-Retamozo Virna1,Panizzi Peter1,Figueiredo Jose-Luiz1,Kohler Rainer H.1,Chudnovskiy Aleksey1,Waterman Peter1,Aikawa Elena1,Mempel Thorsten R.13,Libby Peter45,Weissleder Ralph16,Pittet Mikael J.1

Affiliation:

1. Center for Systems Biology, Massachusetts General Hospital and Harvard Medical School, Boston, MA 02114, USA.

2. Faculty of Biology and Medicine, University of Lausanne, CH-1015 Lausanne, Switzerland.

3. Center for Immunology and Inflammatory Diseases, Massachusetts General Hospital and Harvard Medical School, Charlestown, MA 02129, USA.

4. Cardiovascular Division, Department of Medicine, Brigham and Women’s Hospital, Boston, MA 02115, USA.

5. Center for Excellence in Vascular Biology, Brigham and Women’s Hospital, Boston, MA 02115, USA.

6. Department of Systems Biology, Harvard Medical School, Boston, MA 02115.

Abstract

Monitoring Monocyte Reservoirs Monocytes are cells of the immune system that are recruited to sites of tissue injury and inflammation where they help to resolve the infection and are important for tissue repair. The bone marrow and blood are believed to be the primary reservoirs from which monocytes are mobilized after injury. Swirski et al. (p. 612 ; see the Perspective by Jia and Pamer ) now demonstrate that the spleen also serves as a critical reservoir of monocytes that are recruited during ischemic myocardial injury. Monocytes in the spleen are very similar in phenotype to blood-derived monocytes and are mobilized to the injured heart, where they represent a large fraction of the total monocytes that are recruited. The chemoattractant, angiotensin II, is required for optimal monocyte mobilization from the spleen and emigration into injured tissue.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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