참고문헌
- Banchereau, J., and Steinman, R.M. (1998). Dendritic cells and the control of immunity. Nature 392, 245-252. https://doi.org/10.1038/32588
- Becker, L., Liu, N.C., Averill, M.M., Yuan, W., Pamir, N., Peng, Y., Irwin, A.D., Fu, X., Bornfeldt, K.E., and Heinecke, J.W. (2012). Unique proteomic signatures distinguish macrophages and dendritic cells. PLoS One 7, e33297. https://doi.org/10.1371/journal.pone.0033297
- Bhattacharya, P., Gopisetty, A., Ganesh, B.B., Sheng, J.R., and Prabhakar, B.S. (2011). GM-CSF-induced, bone-marrow-derived dendritic cells can expand natural Tregs and induce adaptive Tregs by different mechanisms. J. Leukocyte Biol. 89, 235-249. https://doi.org/10.1189/jlb.0310154
- Cebon, J., Layton, J.E., Maher, D., and Morstyn, G. (1994). Endogenous haemopoietic growth factors in neutropenia and infection. Br. J. Haematol. 86, 265-274. https://doi.org/10.1111/j.1365-2141.1994.tb04725.x
- Cheers, C., Haigh, A.M., Kelso, A., Metcalf, D., Stanley, E.R., and Young, A.M. (1988). Production of colony-stimulating factors (CSFs) during infection: separate determinations of macrophage-, granulocyte-, granulocyte-macrophage-, and multi-CSFs. Infect. Immun. 56, 247-251.
- Chung, S., Ranjan, R., Lee, Y.G., Park, G.Y., Karpurapu, M., Deng, J., Xiao, L., Kim, J.Y., Unterman, T.G., and Christman, J.W. (2015). Distinct role of FoxO1 in M-CSF- and GM-CSF-differentiated macrophages contributes LPS-mediated IL-10: implication in hyperglycemia. J. Leukocyte Biol. 97, 327-339. https://doi.org/10.1189/jlb.3A0514-251R
- Crozat, K., Guiton, R., Guilliams, M., Henri, S., Baranek, T., Schwartz-Cornil, I., Malissen, B., and Dalod, M. (2010). Comparative genomics as a tool to reveal functional equivalences between human and mouse dendritic cell subsets. Immunol. Rev. 234, 177-198. https://doi.org/10.1111/j.0105-2896.2009.00868.x
- Egawa, M., Mukai, K., Yoshikawa, S., Iki, M., Mukaida, N., Kawano, Y., Minegishi, Y., and Karasuyama, H. (2013). Inflammatory monocytes recruited to allergic skin acquire an anti-inflammatory M2 phenotype via basophil-derived interleukin-4. Immunity 38, 570-580. https://doi.org/10.1016/j.immuni.2012.11.014
- Fleetwood, A.J., Lawrence, T., Hamilton, J.A., and Cook, A.D. (2007). Granulocyte-macrophage colony-stimulating factor (CSF) and macrophage CSF-dependent macrophage phenotypes display differences in cytokine profiles and transcription factor activities: implications for CSF blockade in inflammation. J. Immunol. 178, 5245-5252. https://doi.org/10.4049/jimmunol.178.8.5245
- Ganesh, B.B., Cheatem, D.M., Sheng, J.R., Vasu, C., and Prabhakar, B.S. (2009). GM-CSF-induced CD11c+CD8a--dendritic cells facilitate Foxp3+ and IL-10+ regulatory T cell expansion resulting in suppression of autoimmune thyroiditis. Int. Immunol. 21, 269-282. https://doi.org/10.1093/intimm/dxn147
- Gautier, E.L., Shay, T., Miller, J., Greter, M., Jakubzick, C., Ivanov, S., Helft, J., Chow, A., Elpek, K.G., Gordonov, S., et al. (2012). Gene-expression profiles and transcriptional regulatory pathways that underlie the identity and diversity of mouse tissue macrophages. Nat. Immunol. 13, 1118-1128. https://doi.org/10.1038/ni.2419
- Hashimoto, D., Miller, J., and Merad, M. (2011). Dendritic cell and macrophage heterogeneity in vivo. Immunity 35, 323-335. https://doi.org/10.1016/j.immuni.2011.09.007
- Helft, J., Bottcher, J., Chakravarty, P., Zelenay, S., Huotari, J., Schraml, B.U., Goubau, D., and Reis e Sousa, C. (2015). GMCSF 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
- Heng, T.S., Painter, M.W., and Immunological Genome Project, C. (2008). The Immunological Genome Project: networks of gene expression in immune cells. Nat. Immunol. 9, 1091-1094. https://doi.org/10.1038/ni1008-1091
- Hercus, T.R., Thomas, D., Guthridge, M.A., Ekert, P.G., King-Scott, J., Parker, M.W., and Lopez, A.F. (2009). The granulocytemacrophage colony-stimulating factor receptor: linking its structure to cell signaling and its role in disease. Blood 114, 1289-1298. https://doi.org/10.1182/blood-2008-12-164004
- Inaba, K., Inaba, M., Deguchi, M., Hagi, K., Yasumizu, R., Ikehara, S., Muramatsu, S., and Steinman, R.M. (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. USA 90, 3038-3042. https://doi.org/10.1073/pnas.90.7.3038
- Mellman, I., and Steinman, R.M. (2001). Dendritic cells: specialized and regulated antigen processing machines. Cell 106, 255-258. https://doi.org/10.1016/S0092-8674(01)00449-4
- Miller, J.C., Brown, B.D., Shay, T., Gautier, E.L., Jojic, V., Cohain, A., Pandey, G., Leboeuf, M., Elpek, K.G., Helft, J., et al. (2012). Deciphering the transcriptional network of the dendritic cell lineage. Nat. Immunol. 13, 888-899. https://doi.org/10.1038/ni.2370
- Murray, P.J., Allen, J.E., Biswas, S.K., Fisher, E.A., Gilroy, D.W., Goerdt, S., Gordon, S., Hamilton, J.A., Ivashkiv, L.B., Lawrence, T., et al. (2014). Macrophage activation and polarization: nomenclature and experimental guidelines. Immunity 41, 14-20. https://doi.org/10.1016/j.immuni.2014.06.008
- Nikolic, T., de Bruijn, M.F., Lutz, M.B., and Leenen, P.J. (2003). Developmental stages of myeloid dendritic cells in mouse bone marrow. Int. Immunol. 15, 515-524. https://doi.org/10.1093/intimm/dxg050
- Paine, R., 3rd, Morris, S.B., Jin, H., Wilcoxen, S.E., Phare, S.M., Moore, B.B., Coffey, M.J., and Toews, G.B. (2001). Impaired functional activity of alveolar macrophages from GM-CSF-deficient mice. Am. J. Physiol. Lung Cell. Mol. Physiol. 281, L1210-1218. https://doi.org/10.1152/ajplung.2001.281.5.L1210
- Robbins, S.H., Walzer, T., Dembele, D., Thibault, C., Defays, A., Bessou, G., Xu, H., Vivier, E., Sellars, M., Pierre, P., et al. (2008). Novel insights into the relationships between dendritic cell subsets in human and mouse revealed by genome-wide expression profiling. Genome Biol. 9, R17. https://doi.org/10.1186/gb-2008-9-1-r17
- Saraiva, M., and O'Garra, A. (2010). The regulation of IL-10 production by immune cells. Nat. Rev. Immunol. 10, 170-181. https://doi.org/10.1038/nri2711
- Satpathy, A.T., Wu, X., Albring, J.C., and Murphy, K.M. (2012). Re(de)fining the dendritic cell lineage. Nat. Immunol. 13, 1145-1154. https://doi.org/10.1038/ni.2467
- Seok, S.H., Heo, J.I., Hwang, J.H., Na, Y.R., Yun, J.H., Lee, E.H., Park, J.W., and Cho, C.H. (2013). Angiopoietin-1 elicits pro-inflammatory responses in monocytes and differentiating macrophages. Mol. Cells 35, 550-556. https://doi.org/10.1007/s10059-013-0088-8
- Xu, Y., Zhan, Y., Lew, A.M., Naik, S.H., and Kershaw, M.H. (2007). Differential development of murine dendritic cells by GM-CSF versus Flt3 ligand has implications for inflammation and trafficking. J. Immunol. 179, 7577-7584. https://doi.org/10.4049/jimmunol.179.11.7577
- Zhang, Y., Harada, A., Wang, J.B., Zhang, Y.Y., Hashimoto, S., Naito, M., and Matsushima, K. (1998). Bifurcated dendritic cell differentiation in vitro from murine lineage phenotype-negative c-kit+ bone marrow hematopoietic progenitor cells. Blood 92, 118-128.
피인용 문헌
- Loss of lipid phosphatase SHIP1 promotes macrophage differentiation through suppression of dendritic cell differentiation pp.1555-8576, 2018, https://doi.org/10.1080/15384047.2018.1523846
- GM-CSF Quantity Has a Selective Effect on Granulocytic vs. Monocytic Myeloid Development and Function vol.9, pp.1664-3224, 2018, https://doi.org/10.3389/fimmu.2018.01922
- Integrated Network Pharmacology and Metabolomics Analysis of the Therapeutic Effects of Zi Dian Fang on Immune Thrombocytopenic Purpura vol.9, pp.1663-9812, 2018, https://doi.org/10.3389/fphar.2018.00597
- Increased B7-H4 expression during esophageal squamous cell carcinogenesis is associated with IL-6/STAT3 signaling pathway activation in mice vol.13, pp.4, 2016, https://doi.org/10.3892/ol.2017.5688
- Serum amyloid A inhibits dendritic cell differentiation by suppressing GM-CSF receptor expression and signaling vol.49, pp.8, 2017, https://doi.org/10.1038/emm.2017.120
- Listeria monocytogenes Replicate in Bone Marrow–Derived CD11c+ Cells but Not in Dendritic Cells Isolated from the Murine Gastrointestinal Tract vol.199, pp.11, 2016, https://doi.org/10.4049/jimmunol.1700970
- Tolerogenic bone marrow-derived dendritic cells induce neuroprotective regulatory T cells in a model of Parkinson’s disease vol.13, pp.None, 2016, https://doi.org/10.1186/s13024-018-0255-7
- Stable incorporation of GM-CSF into dissolvable microneedle patch improves skin vaccination against influenza vol.276, pp.None, 2018, https://doi.org/10.1016/j.jconrel.2018.02.033
- Development of endocytosis, degradative activity, and antigen processing capacity during GM-CSF driven differentiation of murine bone marrow vol.13, pp.5, 2018, https://doi.org/10.1371/journal.pone.0196591
- Androgen and Androgen Receptor as Enhancers of M2 Macrophage Polarization in Allergic Lung Inflammation vol.201, pp.10, 2018, https://doi.org/10.4049/jimmunol.1800352
- GM-CSF-Dependent Inflammatory Pathways vol.10, pp.None, 2016, https://doi.org/10.3389/fimmu.2019.02055
- The Pleiotropic Effects of the GM-CSF Rheostat on Myeloid Cell Differentiation and Function: More Than a Numbers Game vol.10, pp.None, 2016, https://doi.org/10.3389/fimmu.2019.02679
- MSU Crystals Enhance TDB-Mediated Inflammatory Macrophage IL-1β Secretion vol.42, pp.3, 2019, https://doi.org/10.1007/s10753-019-00976-5
- In vitro cellular responses to Neospora caninum glycosylphosphatidylinositols depend on the host origin of antigen presenting cells vol.119, pp.None, 2016, https://doi.org/10.1016/j.cyto.2019.03.014
- Downregulation of MHC Class II by Ubiquitination Is Required for the Migration of CD206+ Dendritic Cells to Skin-Draining Lymph Nodes vol.203, pp.11, 2019, https://doi.org/10.4049/jimmunol.1900593
- Quantitative MRI cell tracking of immune cell recruitment to tumors and draining lymph nodes in response to anti-PD-1 and a DPX-based immunotherapy vol.9, pp.1, 2016, https://doi.org/10.1080/2162402x.2020.1851539
- GM-CSF in inflammation vol.217, pp.1, 2020, https://doi.org/10.1084/jem.20190945
- Mouse T cell priming is enhanced by maturation-dependent stiffening of the dendritic cell cortex vol.9, pp.None, 2016, https://doi.org/10.7554/elife.55995
- In vitro Chicken Bone Marrow-Derived Dendritic Cells Comprise Subsets at Different States of Maturation vol.11, pp.None, 2020, https://doi.org/10.3389/fimmu.2020.00141
- TLR2 and Dectin-1 Signaling in Mouse Hematopoietic Stem and Progenitor Cells Impacts the Ability of the Antigen Presenting Cells They Produce to Activate CD4 T Cells vol.9, pp.5, 2016, https://doi.org/10.3390/cells9051317
- Allosteric Inhibition of SHP2 Stimulates Antitumor Immunity by Transforming the Immunosuppressive Environment vol.80, pp.13, 2016, https://doi.org/10.1158/0008-5472.can-19-3038
- Granulocyte/Macrophage Colony-Stimulating Factor-Derived Macrophages Exhibit Distinctive Early Immune Response to Lymphocytic Choriomeningitis Virus Infection vol.33, pp.6, 2020, https://doi.org/10.1089/vim.2019.0178
- Control of GM-CSF–Dependent Dendritic Cell Differentiation and Maturation by DEF6 and SWAP-70 vol.205, pp.5, 2020, https://doi.org/10.4049/jimmunol.2000020
- Toll-Like Receptor 2-Tpl2-Dependent ERK Signaling Drives Inverse Interleukin 12 Regulation in Dendritic Cells and Macrophages vol.89, pp.1, 2016, https://doi.org/10.1128/iai.00323-20
- Integrin Alpha E (CD103) Limits Virus-Induced IFN-I Production in Conventional Dendritic Cells vol.11, pp.None, 2016, https://doi.org/10.3389/fimmu.2020.607889
- Carbomer-based adjuvant elicits CD8 T-cell immunity by inducing a distinct metabolic state in cross-presenting dendritic cells vol.17, pp.1, 2016, https://doi.org/10.1371/journal.ppat.1009168
- Mutation in Irf8 Gene (Irf8R294C) Impairs Type I IFN-Mediated Antiviral Immune Response by Murine pDCs vol.12, pp.None, 2016, https://doi.org/10.3389/fimmu.2021.758190
- MRP8/14 mediates macrophage efferocytosis through RAGE and Gas6/MFG‐E8, and induces polarization via TLR4‐dependent pathway vol.236, pp.2, 2016, https://doi.org/10.1002/jcp.29944
- Complement-Opsonized Nano-Carriers Are Bound by Dendritic Cells (DC) via Complement Receptor (CR)3, and by B Cell Subpopulations via CR-1/2, and Affect the Activation of DC and B-1 Cells vol.22, pp.6, 2016, https://doi.org/10.3390/ijms22062869
- Differential TLR7-mediated cytokine expression by R848 in M-CSF- versus GM-CSF-derived macrophages after LCMV infection vol.102, pp.3, 2016, https://doi.org/10.1099/jgv.0.001541
- Combination Adjuvants Affect the Magnitude of Effector-Like Memory CD8 T Cells and Protection against Listeriosis vol.89, pp.7, 2016, https://doi.org/10.1128/iai.00768-20
- Crosstalk between Metabolic Disorders and Immune Cells vol.22, pp.18, 2016, https://doi.org/10.3390/ijms221810017
- Serum amyloid A delivers retinol to intestinal myeloid cells to promote adaptive immunity vol.373, pp.6561, 2016, https://doi.org/10.1126/science.abf9232
- The Sympathetic Nervous System Modulates Cancer Vaccine Activity through Monocyte-Derived Cells vol.207, pp.12, 2021, https://doi.org/10.4049/jimmunol.2100719
- IRF8 and BATF3 interaction enhances the cDC1 specific Pfkfb3 gene expression vol.371, pp.None, 2016, https://doi.org/10.1016/j.cellimm.2021.104468