Splenic red pulp macrophages are intrinsically superparamagnetic and contaminate magnetic cell isolates
Open accessAbstract
A main function of splenic red pulp macrophages is the degradation of damaged or aged erythrocytes. Here we show that these macrophages accumulate ferrimagnetic iron oxides that render them intrinsically superparamagnetic. Consequently, these cells routinely contaminate splenic cell isolates obtained with the use of MCS, a technique that has been widely used in immunological research for decades. These contaminations can profoundly alter experimental results. In mice deficient for the transcription factor SpiC, which lack red pulp macrophages, liver Kupffer cells take over the task of erythrocyte degradation and become superparamagnetic. We describe a simple additional magnetic separation step that avoids this problem and substantially improves purity of magnetic cell isolates from the spleen.
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RPM and KC express the complete machinery for RBC clearance and heme iron recycling.
“It is well established that RPM and KC express the complete machinery for RBC clearance and heme iron recycling [72, 88, 231].”
From “Pumping iron”—how macrophages handle iron at the systemic, microenvironmental, and cellular levels (2017) · cites this paper as [72]
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Structure and function of the spleen
Mebius, R. E., & Kraal, G. (2005) · Nature reviews. Immunology · doi:10.1038/nri1669 · Cited by 2,245 · see citing works
Davies, L. C., Jenkins, S. J., Allen, J. E., & Taylor, P. R. (2013) · Nature Immunology · doi:10.1038/ni.2705 · Cited by 2,096 · see citing works
High gradient magnetic cell separation with MACS
Miltenyi, S., Müller, W., Weichel, W., & Radbruch, A. (1990) · Cytometry · doi:10.1002/cyto.990110203 · Cited by 1,680 · see citing works
Dzionek, A., Fuchs, A., Schmidt, P., Cremer, S., Zysk, M., Miltenyi, S., Buck, D., & Schmitz, J. (2000) · Journal of Immunology · doi:10.4049/jimmunol.165.11.6037 · Cited by 1,433 · see citing works
Steady-state and inflammatory dendritic-cell development
Shortman, K., & Naik, S. H. (2006) · Nature reviews. Immunology · doi:10.1038/nri1996 · Cited by 1,180 · see citing works
Cross‐presentation, dendritic cell subsets, and the generation of immunity to cellular antigens
Heath, W. R., Belz, G., Behrens, G., Smith, C. M., Forehan, S., Parish, I., Davey, G. M., Wilson, N., Carbone, F., & Villadangos, J. (2004) · Immunological Reviews · doi:10.1111/j.0105-2896.2004.00142.x · Cited by 834 · see citing works
Role for Spi-C in the development of red pulp macrophages and splenic iron homeostasis
Kohyama, M., Ise, W., Edelson, B. T., Wilker, P. R., Hildner, K., Mejia, C., Frazier, W. A., Murphy, T. L., & Murphy, K. M. (2009) · Nature · doi:10.1038/nature07472 · Cited by 479 · see citing works
Compensatory dendritic cell development mediated by BATF–IRF interactions
Tussiwand, R., Lee, W.-L., Murphy, T. L., Mashayekhi, M., Wumesh, K. C., Albring, J. C., Satpathy, A. T., Rotondo, J. A., Edelson, B. T., Kretzer, N. M., et al. (2012) · Nature · doi:10.1038/nature11531 · Cited by 419 · see citing works
TLR‐mediated stimulation of APC: Distinct cytokine responses of B cells and dendritic cells
Barr, T. A., Brown, S. L., Ryan, G. A., Zhao, J., & Gray, D. (2007) · European Journal of Immunology · doi:10.1002/eji.200636483 · Cited by 281 · see citing works
Considerations for the control of background fluorescence in clinical flow cytometry
Hulspas, R., O'Gorman, M. R. G., Wood, B. L., Gratama, J. W., & Sutherland, D. R. (2009) · Cytometry Part B: Clinical Cytometry · doi:10.1002/cyto.b.20485 · Cited by 255 · see citing works
Leenen, P. J. M., Radošević, K., Voerman, J. S. A., Salomon, B. L., van Rooijen, N., Klatzmann, D., & van Ewijk, W. (1998) · The Journal of Immunology · doi:10.4049/jimmunol.160.5.2166 · Cited by 254 · see citing works
Schiwon, M., Weisheit, C. K., Franken, L., Gutweiler, S., Dixit, A., Meyer‐Schwesinger, C., Pohl, J., Maurice, N. J., Thiebes, S., Lorenz, K., et al. (2014) · Cell · doi:10.1016/j.cell.2014.01.006 · Cited by 242 · see citing works
Self-citationFaveeuw, C., Fougeray, S., Angéli, V., Fontaine, J., Chinetti, G., Gosset, P., Delerive, P., Maliszewski, C. R., Capron, M., Staels, B., et al. (2000) · FEBS Letters · doi:10.1016/s0014-5793(00)02319-x · Cited by 159 · see citing works
Pang, I. K., Ichinohe, T., & Iwasaki, A. (2013) · Nature Immunology · doi:10.1038/ni.2514 · Cited by 145 · see citing works
Mechanism for phosphatidylserine-dependent erythrophagocytosis in mouse liver
Lee, S.-J., Park, S., Jung, M.-Y., Bae, S. M., & Kim, I.-S. (2011) · Blood · doi:10.1182/blood-2010-10-313239 · Cited by 119 · see citing works
Cloning and characterization of GITR ligand
Kim, J. D., Choi, B. K., Bae, J., et al. (2003) · Genes and Immunity · doi:10.1038/sj.gene.6364026 · Cited by 107 · see citing works
Magnetic properties of monodisperse iron oxide nanoparticles
Lin, C.-R., Chiang, R., Wang, J.-S., & Sung, T. (2006) · Journal of Applied Physics · doi:10.1063/1.2172891 · Cited by 90 · see citing works
Low-frequency low-field magnetic susceptibility of ferritin and hemosiderin
Allen, P. D., Pierre, T. G. S., Chua‐anusorn, W., Ström, V., & Rao, K. V. (2000) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/s0925-4439(99)00104-0 · Cited by 82 · see citing works
Assessment of Cell Viability in Three-Dimensional Scaffolds Using Cellular Auto-Fluorescence
Dittmar, R. R., Potier, E., van Zandvoort, M. A. M. J., et al. (2011) · Tissue Engineering Part C Methods · doi:10.1089/ten.tec.2011.0334 · Cited by 61 · see citing works
CSF-1–Dependent Red Pulp Macrophages Regulate CD4 T Cell Responses
Kurotaki, D., Kon, S., Bae, K., Ito, K., Matsui, Y., Nakayama, Y., Kanayama, M., Kimura, C., Narita, Y., Nishimura, T., et al. (2011) · The Journal of Immunology · doi:10.4049/jimmunol.1001345 · Cited by 58 · see citing works
Bilirubin: an autofluorescence bile biomarker for liver functionality monitoring
Croce, A. C., Ferrigno, A., Santin, G., et al. (2013) · Journal of Biophotonics · doi:10.1002/jbio.201300039 · Cited by 37 · see citing works
Dead or alive? Autofluorescence distinguishes heat-fixed from viable cells
Hennings, L. J., Kaufmann, Y., Griffin, R. J., et al. (2009) · International Journal of Hyperthermia · doi:10.1080/02656730902964357 · Cited by 31 · see citing works
Hepatic Kupffer cell phagocytotic function in rats with erythrocytic‐stage malaria
NOBES, M. S., Ghabrial, H., SIMMS, K. M., Smallwood, R. A., Morgan, D. J., & Sewell, R. B. (2002) · Journal of Gastroenterology and Hepatology · doi:10.1046/j.1440-1746.2002.02742.x · Cited by 21 · see citing works
Haga, Y., Kay, H. D., Tempero, M. A., et al. (1992) · Clinical Biochemistry · doi:10.1016/0009-9120(92)80033-d · Cited by 13 · see citing works
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Hirayama, D., Iida, T., & Nakase, H. (2017) · International Journal of Molecular Sciences · doi:10.3390/ijms19010092 · Cited by 927 · see citing works
“Pumping iron”—how macrophages handle iron at the systemic, microenvironmental, and cellular levels
Nairz, M., Theurl, I., Swirski, F. K., & Weiss, G. (2017) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s00424-017-1944-8 · Cited by 178 · see citing works
Iron induces anti-tumor activity in tumor-associated macrophages
Costa da Silva, M., Breckwoldt, M. O., Vinchi, F., Correia, M. P., Stojanovic, A., Thielmann, C. M., Meister, M., Muley, T., Warth, A., Platten, M., et al. (2017) · Frontiers in Immunology · doi:10.3389/fimmu.2017.01479 · Cited by 164 · see citing works
- Authors
- Franken, L., Klein, M., Spasova, M., Elsukova, A., Wiedwald, U., Welz, M., Knolle, P., Farle, M., Limmer, A., & Kurts, C.
- Affiliations
- University of Bonn (DE)
- University of Duisburg-Essen (DE)
- Technical University of Munich (DE)
- University Hospital Bonn (DE)
- Corresponding author
- Franken, Lars
- Kurts, Christian
- ORCID
- Venue
- Scientific Reports
- Published
- 2015-08-11
- Volume
- 5
- Issue
- 1
- Pages
- 12940-12940
- ISSN
- 2045-2322 (ISSN-L)
- PMC
- PMC4531335
- OpenAlex
- W2285674543
- Cited by
- 54
- References
- 24
- Citations by year
- 2026: 4 · 2025: 4 · 2024: 5 · 2023: 3 · 2022: 3 · 2021: 1 · 2020: 6 · 2019: 8 · 2018: 4 · 2017: 11 · 2016: 5
- FWCI
- 3.31
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Locations
- Scientific Reports (publishedVersion, cc-by)
- Europe PMC (PubMed Central) (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- mediaTUM – the media and publications repository of the Technical University Munich (Technical University Munich) (submittedVersion)
- Funders
- Deutsche Forschungsgemeinschaft (SFBTR57, SFB 704, SFB 645)
- Topics
- Physical Sciences › Engineering › Biomedical Engineering › Characterization and Applications of Magnetic Nanoparticles
- Life Sciences › Immunology and Microbiology › Immunology › Immune cells in cancer
- Health Sciences › Medicine › Hematology › Iron Metabolism and Disorders
- Keywords
- superparamagnetism, Kupffer cells, spleen
- MeSH terms
- Animals, Blood Cell Count, Cell Separation, Erythrocytes, Flow Cytometry, Humans, Liver, Macrophages, Phagocytosis, Spleen, Cell Lineage, Mice, Ferrosoferric Oxide
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