MHC II+ resident peritoneal and pleural macrophages rely on IRF4 for development from circulating monocytes

Journal of Experimental Medicine

Volumn 213, Issue 10, 2016, Pages 1951-1959

  Kim, Ki Wook ^a   Williams, Jesse W ^a   Wang, Ya Ting ^a   Ivanov, Stoyan ^a   Gilfillan, Susan ^a   Colonna, Marco ^a   Virgin, Herbert W ^a   Gautier, Emmanuel L ^b   Randolph, Gwendalyn J ^a  

^a WASHINGTON UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b SORBONNE UNIVERSITÉ   (France)

Author keywords

[No Author keywords available]

Indexed keywords

AMPICILLIN; CD226 ANTIGEN; CHEMOKINE RECEPTOR CCR2; CHEMOKINE RECEPTOR CX3CR1; CRE RECOMBINASE; GLYCOPROTEIN P 15095; INTERFERON REGULATORY FACTOR 4; MAJOR HISTOCOMPATIBILITY ANTIGEN CLASS 2; METRONIDAZOLE; NEOMYCIN; TOLL LIKE RECEPTOR ADAPTOR MOLECULE 2; TRANSCRIPTION FACTOR GATA 6; UNCLASSIFIED DRUG; VANCOMYCIN; ANTIINFECTIVE AGENT; INTERFERON REGULATORY FACTOR; INTERFERON REGULATORY FACTOR-4; T LYMPHOCYTE ANTIGEN;

ADOPTIVE TRANSFER; ADULT; ANIMAL CELL; ANIMAL EXPERIMENT; ANTIBIOTIC THERAPY; ARTICLE; CELL DIFFERENTIATION; CELL MATURATION; CHIMERA; CONTROLLED STUDY; EMBRYO; GENE EXPRESSION; MACROPHAGE; MONOCYTE; MOUSE; NEWBORN; NONHUMAN; PERITONEAL CAVITY; PERITONEUM MACROPHAGE; PLEURA CAVITY; PLEURAL MACROPHAGE; PRIORITY JOURNAL; PROTEIN EXPRESSION; UPREGULATION; ANIMAL; C57BL MOUSE; CYTOLOGY; DRUG EFFECTS; GENE; METABOLISM; PLEURA;

ANIMALS; ANTI-BACTERIAL AGENTS; ANTIGENS, DIFFERENTIATION, T-LYMPHOCYTE; CELL DIFFERENTIATION; GENES, MHC CLASS II; INTERFERON REGULATORY FACTORS; MACROPHAGES, PERITONEAL; MICE; MICE, INBRED C57BL; MONOCYTES; PLEURA; RECEPTORS, CCR2;

EID: 84992215144     PISSN: 00221007     EISSN: 15409538     Source Type: Journal    
DOI: 10.1084/jem.20160486     Document Type: Article

References (30)

1. Baldridge, M.T., T.J. Nice, B.T. McCune, C.C. Yokoyama, A. Kambal, M. Wheadon, M.S. Diamond, Y. Ivanova, M. Artyomov, and H.W. Virgin. 2015. Commensal microbes and interferon-λ determine persistence of enteric murine norovirus infection. Science. 347:266-269. http://dx.doi.org/10.1126/science.1258025
2. Boring, L., J. Gosling, S.W. Chensue, S.L. Kunkel, R.V. Farese Jr., H.E. Broxmeyer, and I.F. Charo. 1997. Impaired monocyte migration and reduced type 1 (Th1) cytokine responses in C-C chemokine receptor 2 knockout mice. J. Clin. Invest. 100:2552-2561. http://dx.doi.org/10.1172/JCI119798
3. Cain, D.W., E.G. O'Koren, M.J. Kan, M. Womble, G.D. Sempowski, K. Hopper, M.D. Gunn, and G. Kelsoe. 2013. Identification of a tissuespecific, C/EBPβ-dependent pathway of differentiation for murine peritoneal macrophages. J. Immunol. 191:4665-4675. http://dx.doi.org/10.4049/jimmunol.1300581
4. Caton, M.L., M.R. Smith-Raska, and B. Reizis. 2007. Notch-RBP-J signaling controls the homeostasis of CD8-dendritic cells in the spleen. J. Exp. Med. 204:1653-1664. http://dx.doi.org/10.1084/jem.20062648
5. Epelman, S., K.J. Lavine, A.E. Beaudin, D.K. Sojka, J.A. Carrero, B. Calderon, T. Brija, E.L. Gautier, S. Ivanov, A.T. Satpathy, et al. 2014a. Embryonic and adult-derived resident cardiac macrophages are maintained through distinct mechanisms at steady state and during inflammation. Immunity. 40:91-104. http://dx.doi.org/10.1016/j.immuni.2013.11.019
6. Epelman, S., K.J. Lavine, and G.J. Randolph. 2014b. Origin and functions of tissue macrophages. Immunity. 41:21-35. http://dx.doi.org/10.1016/j.immuni.2014.06.013
7. Gautier, E.L., T. Shay, J. Miller, M. Greter, C. Jakubzick, S. Ivanov, J. Helft, A. Chow, K.G. Elpek, S. Gordonov, et al. Immunological Genome Consortium. 2012. Gene-expression profiles and transcriptional regulatory pathways that underlie the identity and diversity of mouse tissue macrophages. Nat. Immunol. 13:1118-1128. http://dx.doi.org/10.1038/ni.2419
8. Gautier, E.L., S. Ivanov, J.W. Williams, S.C. Huang, G. Marcelin, K. Fairfax, P.L. Wang, J.S. Francis, P. Leone, D.B. Wilson, et al. 2014. Gata6 regulates aspartoacylase expression in resident peritoneal macrophages and controls their survival. J. Exp. Med. 211:1525-1531. http://dx.doi.org/10.1084/jem.20140570
9. Geissmann, F., S. Jung, and D.R. Littman. 2003. Blood monocytes consist of two principal subsets with distinct migratory properties. Immunity. 19:71-82. http://dx.doi.org/10.1016/S1074-7613(03)00174-2
10. Ghosn, E.E., A.A. Cassado, G.R. Govoni, T. Fukuhara, Y. Yang, D.M. Monack, K.R. Bortoluci, S.R. Almeida, L.A. Herzenberg, and L.A. Herzenberg. 2010. Two physically, functionally, and developmentally distinct peritoneal macrophage subsets. Proc. Natl. Acad. Sci. USA. 107:2568-2573. http://dx.doi.org/10.1073/pnas.0915000107
11. Gilfillan, S., C.J. Chan, M. Cella, N.M. Haynes, A.S. Rapaport, K.S. Boles, D.M. Andrews, M.J. Smyth, and M. Colonna. 2008. DNAM-1 promotes activation of cytotoxic lymphocytes by nonprofessional antigenpresenting cells and tumors. J. Exp. Med. 205:2965-2973. http://dx.doi.org/10.1084/jem.20081752
12. Ginhoux, F., and M. Guilliams. 2016. Tissue-resident macrophage ontogeny and homeostasis. Immunity. 44:439-449. http://dx.doi.org/10.1016/j.immuni.2016.02.024
13. Hashimoto, D., A. Chow, C. Noizat, P. Teo, M.B. Beasley, M. Leboeuf, C.D. Becker, P. See, J. Price, D. Lucas, et al. 2013. Tissue-resident macrophages self-maintain locally throughout adult life with minimal contribution from circulating monocytes. Immunity. 38:792-804. http://dx.doi.org/10.1016/j.immuni.2013.04.004
14. Ingersoll, M.A., R. Spanbroek, C. Lottaz, E.L. Gautier, M. Frankenberger, R. Hoffmann, R. Lang, M. Haniffa, M. Collin, F. Tacke, et al. 2010. Comparison of gene expression profiles between human and mouse monocyte subsets. Blood. 115:e10-e19. http://dx.doi.org/10.1182/blood-2009-07-235028
15. Jung, S., J. Aliberti, P. Graemmel, M.J. Sunshine, G.W. Kreutzberg, A. Sher, and D.R. Littman. 2000. Analysis of fractalkine receptor CX3CR1 function by targeted deletion and green fluorescent protein reporter gene insertion. Mol. Cell. Biol. 20:4106-4114. http://dx.doi.org/10.1128/MCB.20.11.4106-4114.2000
16. Klein, U., S. Casola, G. Cattoretti, Q. Shen, M. Lia, T. Mo, T. Ludwig, K. Rajewsky, and R. Dalla-Favera. 2006. Transcription factor IRF4 controls plasma cell differentiation and class-switch recombination. Nat. Immunol. 7:773-782. http://dx.doi.org/10.1038/ni1357
17. Lavin, Y., A. Mortha, A. Rahman, and M. Merad. 2015. Regulation of macrophage development and function in peripheral tissues. Nat. Rev. Immunol. 15:731-744. http://dx.doi.org/10.1038/nri3920
18. Lindquist, R.L., G. Shakhar, D. Dudziak, H. Wardemann, T. Eisenreich, M.L. Dustin, and M.C. Nussenzweig. 2004. Visualizing dendritic cell networks in vivo. Nat. Immunol. 5:1243-1250. http://dx.doi.org/10.1038/ni1139
19. Liu, K., G.D. Victora, T.A. Schwickert, P. Guermonprez, M.M. Meredith, K. Yao, F.F. Chu, G.J. Randolph, A.Y. Rudensky, and M. Nussenzweig. 2009. In vivo analysis of dendritic cell development and homeostasis. Science. 324:392-397. http://dx.doi.org/10.1126/science.1170540
20. Madisen, L., T.A. Zwingman, S.M. Sunkin, S.W. Oh, H.A. Zariwala, H. Gu, L.L. Ng, R.D. Palmiter, M.J. Hawrylycz, A.R. Jones, et al. 2010. A robust and high-throughput Cre reporting and characterization system for the whole mouse brain. Nat. Neurosci. 13:133-140. http://dx.doi.org/10.1038/nn.2467
21. Molawi, K., Y. Wolf, P.K. Kandalla, J. Favret, N. Hagemeyer, K. Frenzel, A.R. Pinto, K. Klapproth, S. Henri, B. Malissen, et al. 2014. Progressive replacement of embryo-derived cardiac macrophages with age. J. Exp. Med. 211:2151-2158. http://dx.doi.org/10.1084/jem.20140639
22. Newson, J., M. Stables, E. Karra, F. Arce-Vargas, S. Quezada, M. Motwani, M. Mack, S. Yona, T. Audzevich, and D.W. Gilroy. 2014. Resolution of acute inflammation bridges the gap between innate and adaptive immunity. Blood. 124:1748-1764. http://dx.doi.org/10.1182/blood-2014-03-562710
23. Okabe, Y., and R. Medzhitov. 2014. Tissue-specific signals control reversible program of localization and functional polarization of macrophages. Cell. 157:832-844. http://dx.doi.org/10.1016/j.cell.2014.04.016
24. Rosas, M., L.C. Davies, P.J. Giles, C.T. Liao, B. Kharfan, T.C. Stone, V.B. O'Donnell, D.J. Fraser, S.A. Jones, and P.R. Taylor. 2014. The transcription factor Gata6 links tissue macrophage phenotype and proliferative renewal. Science. 344:645-648. http://dx.doi.org/10.1126/science.1251414
25. Satpathy, A.T., C.G. Briseño, J.S. Lee, D. Ng, N.A. Manieri, W. Kc, X. Wu, S.R. Thomas, W.L. Lee, M. Turkoz, et al. 2013. Notch2-dependent classical dendritic cells orchestrate intestinal immunity to attaching-and-effacing bacterial pathogens. Nat. Immunol. 14:937-948. http://dx.doi.org/10.1038/ni.2679
26. Schneider, C., S.P. Nobs, M. Kurrer, H. Rehrauer, C. Thiele, and M. Kopf. 2014. Induction of the nuclear receptor PPAR-γ by the cytokine GMCSF is critical for the differentiation of fetal monocytes into alveolar macrophages. Nat. Immunol. 15:1026-1037. http://dx.doi.org/10.1038/ni.3005
27. Schulz, C., E. Gomez Perdiguero, L. Chorro, H. Szabo-Rogers, N. Cagnard, K. Kierdorf, M. Prinz, B. Wu, S.E. Jacobsen, J.W. Pollard, et al. 2012. A lineage of myeloid cells independent of Myb and hematopoietic stem cells. Science. 336:86-90. http://dx.doi.org/10.1126/science.1219179
28. Serbina, N.V., and E.G. Pamer. 2006. Monocyte emigration from bone marrow during bacterial infection requires signals mediated by chemokine receptor CCR2. Nat. Immunol. 7:311-317. http://dx.doi.org/10.1038/ni1309
29. Tamoutounour, S., M. Guilliams, F. Montanana Sanchis, H. Liu, D. Terhorst, C. Malosse, E. Pollet, L. Ardouin, H. Luche, C. Sanchez, et al. 2013. Origins and functional specialization of macrophages and of conventional and monocyte-derived dendritic cells in mouse skin. Immunity. 39:925-938. http://dx.doi.org/10.1016/j.immuni.2013.10.004
30. Yona, S., K.W. Kim, Y. Wolf, A. Mildner, D. Varol, M. Breker, D. Strauss-Ayali, S. Viukov, M. Guilliams, A. Misharin, et al. 2013. Fate mapping reveals origins and dynamics of monocytes and tissue macrophages under homeostasis. Immunity. 38:79-91. (published erratum appears in Immunity. 2013. 38:1073-1079.) http://dx.doi.org/10.1016/j.immuni.2012.12.001