Identification of splenic reservoir monocytes and their deployment to inflammatory sites
Open accessAbstract
A current paradigm states that monocytes circulate freely and patrol blood vessels but differentiate irreversibly into dendritic cells (DCs) or macrophages upon tissue entry. Here we show that bona fide undifferentiated monocytes reside in the spleen and outnumber their equivalents in circulation. The reservoir monocytes assemble in clusters in the cords of the subcapsular red pulp and are distinct from macrophages and DCs. In response to ischemic myocardial injury, splenic monocytes increase their motility, exit the spleen en masse, accumulate in injured tissue, and participate in wound healing. These observations uncover a role for the spleen as a site for storage and rapid deployment of monocytes and identify splenic monocytes as a resource that the body exploits to regulate inflammation.
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These monocytes derive from the peripheral blood and from pools in the bone marrow and possibly in the spleen.
“These monocytes derive from the peripheral blood and from pools in the BM and possibly in the spleen (Swirski et al., 2009).”
From Iron in infection and immunity (2020) · cites this paper as Swirski et al., 2009
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Nonmyogenic Cells in Skeletal Muscle Regeneration
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Imaging macrophage development and fate in atherosclerosis and myocardial infarction
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- Authors
- Swirski, F. K., Nahrendorf, M., Etzrodt, M., Wildgruber, M., Cortez-Retamozo, V., Panizzi, P., Figueiredo, J.-L., Kohler, R. H., Chudnovskiy, A., Waterman, P., Aikawa, E., Mempel, T. R., Libby, P., Weissleder, R., & Pittet, M. J.
- Affiliations
- Center for Systems Biology, Massachusetts General Hospital and Harvard Medical School, Boston, MA 02114, USA.
- Harvard University (US)
- Brigham and Women's Hospital (US)
- Corresponding author
- Nahrendorf, Matthias
- Weissleder, Ralph
- ORCID
- Venue
- Science
- Published
- 2009-07-31
- Volume
- 325
- Issue
- 5940
- Pages
- 612-616
- ISSN
- 0036-8075 (ISSN-L)
- 1095-9203
- PMC
- PMC2803111
- OpenAlex
- W2003870922
- Cited by
- 2,221
- References
- 27
- Citations by year
- 2026: 72 · 2025: 92 · 2024: 130 · 2023: 125 · 2022: 134 · 2021: 147 · 2020: 148 · 2019: 137 · 2018: 151 · 2017: 167 · 2016: 158 · 2015: 131 · 2014: 169 · 2013: 135 · 2012: 129
- FWCI
- 46.36
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Science (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Archive ouverte UNIGE (University of Geneva) (acceptedVersion, other-oa)
- Digital Access to Scholarship at Harvard (DASH) (Harvard University) (submittedVersion, cc-by)
- Funders
- U.S. Public Health Service (P01 A154904)
- National Heart, Lung, and Blood Institute (U01HL080731, R01HL095629, R00HL094533, R01HL096576, R01HL095612)
- National Cancer Institute (P50-CA-86355, P50CA086355, R24 CA69246, U54CA126515)
- National Institute of Allergy and Infectious Diseases (P01AI054904)
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › Immune cells in cancer
- Life Sciences › Immunology and Microbiology › Immunology › Atherosclerosis and Cardiovascular Diseases
- Life Sciences › Immunology and Microbiology › Immunology › Phagocytosis and Immune Regulation
- Keywords
- splenic monocytes, monocyte mobilization, myocardial ischemic injury, wound healing, inflammation, monocyte differentiation, dendritic cells, macrophages
- MeSH terms
- Angiotensin II, Animals, Antigens, Ly, Bone Marrow Cells, Cell Differentiation, Cell Movement, Female, Inflammation, Mice, Inbred C57BL, Monocytes, Myocardial Infarction, Myocardium, Receptors, Angiotensin, Spleen, Splenectomy, Rats, Wistar, Cell Size, Mice, Rats
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