Defining GM-CSF- and Macrophage-CSF Dependent Macrophage Responses by In Vitro Models

被引:410
作者
Lacey, Derek C. [1 ]
Achuthan, Adrian [1 ]
Fleetwood, Andrew J. [1 ]
Dinh, Hang [1 ]
Roiniotis, John [1 ]
Scholz, Glen M. [1 ]
Chang, Melody W. [1 ]
Beckman, Sandra K. [1 ]
Cook, Andrew D. [1 ]
Hamilton, John A. [1 ]
机构
[1] Univ Melbourne, Royal Melbourne Hosp, Dept Med, Arthrit & Inflammat Res Ctr, Parkville, Vic 3050, Australia
基金
英国医学研究理事会;
关键词
COLONY-STIMULATING FACTOR; DENDRITIC CELL SUBSETS; GENE-EXPRESSION; HUMAN MONOCYTES; DIFFERENTIATION; POLARIZATION; MURINE; INFLAMMATION; MOUSE; INTERLEUKIN-10;
D O I
10.4049/jimmunol.1103426
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
GM-CSF and M-CSF (CSF-1) induce different phenotypic changes in macrophage lineage populations. The nature, extent, and generality of these differences were assessed by comparing the responses to these CSFs, either alone or in combination, in various human and murine macrophage lineage populations. The differences between the respective global gene expression profiles of macrophages, derived from human monocytes by GM-CSF or M-CSF, were compared with the differences between the respective profiles for macrophages, derived from murine bone marrow cells by each CSF. Only 17% of genes regulated differently by these CSFs were common across the species. Whether a particular change in relative gene expression is by direct action of a CSF can be confounded by endogenous mediators, such as type I IFN, IL-10, and activin A. Time-dependent differences in cytokine gene expression were noted in human monocytes treated with the CSFs; in this system, GM-CSF induced a more dramatic expression of IFN-regulated factor 4 (IRF4) than of IRF5, whereas M-CSF induced IRF5 but not IRF4. In the presence of both CSFs, some evidence of "competition" at the level of gene expression was observed. Care needs to be exercised when drawing definitive conclusions from a particular in vitro system about the roles of GM-CSF and M-CSF in macrophage lineage biology. The Journal of Immunology, 2012, 188: 5752-5765.
引用
收藏
页码:5752 / 5765
页数:14
相关论文
共 52 条
[1]
Functional heterogeneity of colony-stimulating factor-induced human monocyte-derived macrophages [J].
Akagawa, KS .
INTERNATIONAL JOURNAL OF HEMATOLOGY, 2002, 76 (01) :27-34
[2]
Gene Ontology: tool for the unification of biology [J].
Ashburner, M ;
Ball, CA ;
Blake, JA ;
Botstein, D ;
Butler, H ;
Cherry, JM ;
Davis, AP ;
Dolinski, K ;
Dwight, SS ;
Eppig, JT ;
Harris, MA ;
Hill, DP ;
Issel-Tarver, L ;
Kasarskis, A ;
Lewis, S ;
Matese, JC ;
Richardson, JE ;
Ringwald, M ;
Rubin, GM ;
Sherlock, G .
NATURE GENETICS, 2000, 25 (01) :25-29
[3]
Minimum information about a microarray experiment (MIAME) - toward standards for microarray data [J].
Brazma, A ;
Hingamp, P ;
Quackenbush, J ;
Sherlock, G ;
Spellman, P ;
Stoeckert, C ;
Aach, J ;
Ansorge, W ;
Ball, CA ;
Causton, HC ;
Gaasterland, T ;
Glenisson, P ;
Holstege, FCP ;
Kim, IF ;
Markowitz, V ;
Matese, JC ;
Parkinson, H ;
Robinson, A ;
Sarkans, U ;
Schulze-Kremer, S ;
Stewart, J ;
Taylor, R ;
Vilo, J ;
Vingron, M .
NATURE GENETICS, 2001, 29 (04) :365-371
[4]
Antagonistic regulation of macrophage phenotype by M-CSF and GM-CSF: Implication in atherosclerosis [J].
Brocheriou, Isabelle ;
Maouche, Seraya ;
Durand, Herve ;
Braunersreuther, Vincent ;
Le Naour, Gilles ;
Gratchev, Alexei ;
Koskas, Fabien ;
Mach, Francois ;
Kzhyshkowska, Julia ;
Ninio, Ewa .
ATHEROSCLEROSIS, 2011, 214 (02) :316-324
[5]
BURGESS AW, 1980, BLOOD, V56, P947
[6]
Cutting edge: Involvement of the type IIFN production and signaling pathway in lipopolysaccharide-induced IL-10 production [J].
Chang, Elmer Y. ;
Guo, Beichu ;
Doyle, Sean E. ;
Cheng, Genhong .
JOURNAL OF IMMUNOLOGY, 2007, 178 (11) :6705-6709
[7]
Colony-stimulating factor-1 in immunity and inflammation [J].
Chitu, V ;
Stanley, ER .
CURRENT OPINION IN IMMUNOLOGY, 2006, 18 (01) :39-48
[8]
Comparative genomics as a tool to reveal functional equivalences between human and mouse dendritic cell subsets [J].
Crozat, Karine ;
Guiton, Rachel ;
Guilliams, Martin ;
Henri, Sandrine ;
Baranek, Thomas ;
Schwartz-Cornil, Isabelle ;
Malissen, Bernard ;
Dalod, Marc .
IMMUNOLOGICAL REVIEWS, 2010, 234 :177-198
[9]
Use of bone marrow-derived macrophages to model murine innate immune responses [J].
Cunnick, Jess ;
Kaur, Pavinder ;
Cho, YoungJin ;
Groffen, John ;
Heisterkamp, Nora .
JOURNAL OF IMMUNOLOGICAL METHODS, 2006, 311 (1-2) :96-105
[10]
Failure of monocytes of trauma patients to convert to immature dendritic cells is related to preferential macrophage-colony-stimulating factor-driven macrophage differentiation [J].
De, AK ;
Laudanski, K ;
Miller-Graziano, CL .
JOURNAL OF IMMUNOLOGY, 2003, 170 (12) :6355-6362