In Vitro Generation of Murine Bone Marrow-Derived Dendritic Cells.


Journal

Methods in molecular biology (Clifton, N.J.)
ISSN: 1940-6029
Titre abrégé: Methods Mol Biol
Pays: United States
ID NLM: 9214969

Informations de publication

Date de publication:
2023
Historique:
entrez: 11 3 2023
pubmed: 12 3 2023
medline: 15 3 2023
Statut: ppublish

Résumé

Dendritic cells (DCs) are mononuclear phagocytes of hematopoietic origin residing in lymphoid and nonlymphoid tissues. DCs are often referred as the sentinels of the immune system as they can sense pathogens and danger signals. Upon activation, DCs migrate to the draining lymph nodes and present antigens to naïve T cells to trigger adaptive immunity. Hematopoietic progenitors for DCs reside in the adult bone marrow (BM). Therefore, BM cell culture systems have been developed to generate large amounts of primary DCs in vitro conveniently enabling to analyze their developmental and functional features. Here, we review various protocols enabling to generate DCs in vitro from murine BM cells and discuss the cellular heterogeneity of each culture system.

Identifiants

pubmed: 36905510
doi: 10.1007/978-1-0716-2938-3_6
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

83-92

Informations de copyright

© 2023. The Author(s), under exclusive license to Springer Science+Business Media, LLC, part of Springer Nature.

Références

Merad M, Sathe P, Helft J, Miller J, Mortha A (2013) The dendritic cell lineage: ontogeny and function of dendritic cells and their subsets in the steady state and the inflamed setting. Annu Rev Immunol 31:563–604. https://doi.org/10.1146/annurev-immunol-020711-074950
doi: 10.1146/annurev-immunol-020711-074950 pubmed: 23516985
Guermonprez P, Gerber-Ferder Y, Vaivode K, Bourdely P, Helft J (2019) Origin and development of classical dendritic cells. Int Rev Cell Mol Biol 349:1–54. https://doi.org/10.1016/bs.ircmb.2019.08.002
doi: 10.1016/bs.ircmb.2019.08.002 pubmed: 31759429
Naik SH, Sathe P, Park H-Y, Metcalf D, Proietto AI, Dakic A, Carotta S, O’Keeffe M, Bahlo M, Papenfuss A et al (2007) Development of plasmacytoid and conventional dendritic cell subtypes from single precursor cells derived in vitro and in vivo. Nat Immunol 8:1217–1226. https://doi.org/10.1038/ni1522
doi: 10.1038/ni1522 pubmed: 17922015
Onai N, Obata-Onai A, Schmid MA, Ohteki T, Jarrossay D, Manz MG (2007) Identification of clonogenic common Flt3+M-CSFR+ plasmacytoid and conventional dendritic cell progenitors in mouse bone marrow. Nat Immunol 8:1207–1216. https://doi.org/10.1038/ni1518
doi: 10.1038/ni1518 pubmed: 17922016
McKenna HJ, Stocking KL, Miller RE, Brasel K, De Smedt T, Maraskovsky E, Maliszewski CR, Lynch DH, Smith J, Pulendran B et al (2000) Mice lacking flt3 ligand have deficient hematopoiesis affecting hematopoietic progenitor cells, dendritic cells, and natural killer cells. Blood 95:3489–3497
Becher B, Tugues S, Greter M (2016) GM-CSF: from growth factor to central mediator of tissue inflammation. Immunity 45:963–973. https://doi.org/10.1016/j.immuni.2016.10.026
doi: 10.1016/j.immuni.2016.10.026 pubmed: 27851925
Helft J, Böttcher J, Chakravarty P, Zelenay S, Huotari J, Schraml BU, Goubau D, Reis e Sousa C (2015) GM-CSF mouse bone marrow cultures comprise a heterogeneous population of CD11c+MHCII+ macrophages and dendritic cells. Immunity 42:1197–1211. https://doi.org/10.1016/j.immuni.2015.05.018
doi: 10.1016/j.immuni.2015.05.018 pubmed: 26084029
Menezes S, Melandri D, Anselmi G, Perchet T, Loschko J, Dubrot J, Patel R, Gautier EL, Hugues S, Longhi MP et al (2016) The heterogeneity of Ly6Chi monocytes controls their differentiation into iNOS+ macrophages or monocyte-derived dendritic cells. Immunity 45:1205–1218. https://doi.org/10.1016/j.immuni.2016.12.001
doi: 10.1016/j.immuni.2016.12.001 pubmed: 28002729 pmcid: 5196026
Inaba K, Inaba M, Romani N, Aya H, Deguchi M, Ikehara S, Muramatsu S, Steinman RM (1992) Generation of large numbers of dendritic cells from mouse bone marrow cultures supplemented with granulocyte/macrophage colony-stimulating factor. J Exp Med 176:1693–1702. https://doi.org/10.1084/jem.176.6.1693
doi: 10.1084/jem.176.6.1693 pubmed: 1460426
Inaba K, Inaba M, Deguchi M, Hagi K, Yasumizu R, Ikehara S, Muramatsu S, Steinman RM (1993) Granulocytes, macrophages, and dendritic cells arise from a common major histocompatibility complex class II-negative progenitor in mouse bone marrow. Proc Natl Acad Sci U S A 90:3038–3042. https://doi.org/10.1073/pnas.90.7.3038
doi: 10.1073/pnas.90.7.3038 pubmed: 8464920 pmcid: 46232
Gao Y, Nish SA, Jiang R, Hou L, Licona-Limón P, Weinstein JS, Zhao H, Medzhitov R (2013) Control of T helper 2 responses by transcription factor IRF4-dependent dendritic cells. Immunity 39:722–732. https://doi.org/10.1016/j.immuni.2013.08.028
doi: 10.1016/j.immuni.2013.08.028 pubmed: 24076050 pmcid: 4110745
Helft J, Böttcher JP, Chakravarty P, Zelenay S, Huotari J, Schraml BU, Goubau D, Reis e Sousa C (2016) Alive but confused: heterogeneity of CD11c(+) MHC class II(+) cells in GM-CSF mouse bone marrow cultures. Immunity 44:3–4. https://doi.org/10.1016/j.immuni.2015.12.014
doi: 10.1016/j.immuni.2015.12.014 pubmed: 26789913
Miller JC, Brown BD, Shay T, Gautier EL, Jojic V, Cohain A, Pandey G, Leboeuf M, Elpek KG, Helft J, Hashimoto D, Chow A, Price J, Greter M, Bogunovic M, Bellemare-Pelletier A, Frenette PS, Randolph GJ, Turley SJ, Merad M (2012) Immunological genome consortium. Deciphering the transcriptional network of the dendritic cell lineage. Nat Immunol 13(9):888–899. https://doi.org/10.1038/ni.2370 . Epub 2012 Jul 15. PMID: 22797772; PMCID: PMC3985403
Katzenelenbogen Y, Sheban F, Yalin A, Yofe I, Svetlichnyy D, Jaitin DA, Bornstein C, Moshe A, Keren-Shaul H, Cohen M et al (2020) Coupled scRNA-Seq and intracellular protein activity reveal an immunosuppressive role of trem2 in cancer. Cell 182:872–885.e19. https://doi.org/10.1016/j.cell.2020.06.032
doi: 10.1016/j.cell.2020.06.032 pubmed: 32783915
Faure-André G, Vargas P, Yuseff M-I, Heuzé M, Diaz J, Lankar D, Steri V, Manry J, Hugues S, Vascotto F et al (2008) Regulation of dendritic cell migration by CD74, the MHC class II-associated invariant chain. Science 322:1705–1710. https://doi.org/10.1126/science.1159894
doi: 10.1126/science.1159894 pubmed: 19074353
Sallusto F, Lanzavecchia A (1994) Efficient presentation of soluble antigen by cultured human dendritic cells is maintained by granulocyte/macrophage colony-stimulating factor plus interleukin 4 and downregulated by tumor necrosis factor alpha. J Exp Med 179:1109–1118. https://doi.org/10.1084/jem.179.4.1109
doi: 10.1084/jem.179.4.1109 pubmed: 8145033
Briseño CG, Haldar M, Kretzer NM, Wu X, Theisen DJ, Kc W, Durai V, Grajales-Reyes GE, Iwata A, Bagadia P et al (2016) Distinct transcriptional programs control cross-priming in classical and monocyte-derived dendritic cells. Cell Rep 15:2462–2474. https://doi.org/10.1016/j.celrep.2016.05.025
doi: 10.1016/j.celrep.2016.05.025 pubmed: 27264183 pmcid: 4941620
Vander Lugt B, Khan AA, Hackney JA, Agrawal S, Lesch J, Zhou M, Lee WP, Park S, Xu M, DeVoss J et al (2014) Transcriptional programming of dendritic cells for enhanced MHC class II antigen presentation. Nat Immunol 15:161–167. https://doi.org/10.1038/ni.2795
doi: 10.1038/ni.2795 pubmed: 24362890
Lewis KL, Caton ML, Bogunovic M, Greter M, Grajkowska LT, Ng D, Klinakis A, Charo IF, Jung S, Gommerman JL et al (2011) Notch2 receptor signaling controls functional differentiation of dendritic cells in the spleen and intestine. Immunity 35:780–791. https://doi.org/10.1016/j.immuni.2011.08.013
doi: 10.1016/j.immuni.2011.08.013 pubmed: 22018469 pmcid: 3225703
Tussiwand R, Everts B, Grajales-Reyes GE, Kretzer NM, Iwata A, Bagaitkar J, Wu X, Wong R, Anderson DA, Murphy TL et al (2015) Klf4 expression in conventional dendritic cells is required for T helper 2 cell responses. Immunity 42:916–928. https://doi.org/10.1016/j.immuni.2015.04.017
doi: 10.1016/j.immuni.2015.04.017 pubmed: 25992862 pmcid: 4447135
Sathe P, Metcalf D, Vremec D, Naik SH, Langdon WY, Huntington ND, Wu L, Shortman K (2014) Lymphoid tissue and plasmacytoid dendritic cells and macrophages do not share a common macrophage-dendritic cell-restricted progenitor. Immunity 41:104–115. https://doi.org/10.1016/j.immuni.2014.05.020
doi: 10.1016/j.immuni.2014.05.020 pubmed: 25035955
Sathe P, Pooley J, Vremec D, Mintern J, Jin J-O, Wu L, Kwak J-Y, Villadangos JA, Shortman K (2011) The acquisition of antigen cross-presentation function by newly formed dendritic cells. J Immunol 186:5184–5192. https://doi.org/10.4049/jimmunol.1002683
doi: 10.4049/jimmunol.1002683 pubmed: 21422244
Mayer CT, Ghorbani P, Nandan A, Dudek M, Arnold-Schrauf C, Hesse C, Berod L, Stuve P, Puttur F, Merad M et al (2014) Selective and efficient generation of functional Batf3-dependent CD103+ dendritic cells from mouse bone marrow. Blood 124:3081–3091. https://doi.org/10.1182/blood-2013-12-545772
doi: 10.1182/blood-2013-12-545772 pubmed: 25100743 pmcid: 4260363
Kirkling ME, Cytlak U, Lau CM, Lewis KL, Resteu A, Khodadadi-Jamayran A, Siebel CW, Salmon H, Merad M, Tsirigos A et al (2018) Notch signaling facilitates in vitro generation of cross-presenting classical dendritic cells. Cell Rep 23:3658–3672.e6. https://doi.org/10.1016/j.celrep.2018.05.068
doi: 10.1016/j.celrep.2018.05.068 pubmed: 29925006 pmcid: 6063084

Auteurs

Yohan Gerber-Ferder (Y)

PSL University, Institut Curie Research Center, INSERM U932, Center for Cancers Immunotherapy, Paris, France.

Pierre Bourdely (P)

Université de Paris, Centre for Inflammation Research, CNRS ERL8252, INSERM1149, Paris, France.

Mathias Vetillard (M)

Université de Paris, Centre for Inflammation Research, CNRS ERL8252, INSERM1149, Paris, France.

Pierre Guermonprez (P)

Université de Paris, Centre for Inflammation Research, CNRS ERL8252, INSERM1149, Paris, France.

Julie Helft (J)

PSL University, Institut Curie Research Center, INSERM U932, Center for Cancers Immunotherapy, Paris, France. julie.helft@inserm.fr.
Université de Paris, Centre for Inflammation Research, CNRS ERL8252, INSERM1149, Paris, France. julie.helft@inserm.fr.
Université de Paris - Inserm - Cnrs, Institut Cochin, Paris, France. julie.helft@inserm.fr.

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