The twin cytokines interleukin-34 and CSF-1: masterful conductors of macrophage homeostasis

被引:110
作者
Munoz-Garcia, Javier [1 ,2 ]
Cochonneau, Denis [1 ]
Teletchea, Stephane [3 ]
Moranton, Emilie [1 ]
Lanoe, Didier [1 ]
Brion, Regis [4 ]
Lezot, Frederic [4 ]
Heymann, Marie-Francoise [1 ]
Heymann, Dominique [1 ,5 ]
机构
[1] Univ Nantes, Inst Cancerol Ouest, F-44805 St Herblain, France
[2] SATT Ouest Valorisat, Nantes, France
[3] Univ Nantes, CNRS, UFIP, UMR 6286, Nantes, France
[4] Univ Nantes, U1238, INSERM, Nantes, France
[5] Univ Sheffield, Med Sch, Dept Oncol & Metab, Sheffield, S Yorkshire, England
关键词
IL-34; inflammation; macrophage differentiation; theranostics; tumor; COLONY-STIMULATING FACTOR; TUMOR-ASSOCIATED MACROPHAGES; FACTOR-I RECEPTOR; LANGERHANS CELLS; KEY ROLE; INDUCED OSTEOCLASTOGENESIS; DIFFERENTIAL EXPRESSION; MEDIATED DELIVERY; SYNOVIAL-FLUID; LIVER FIBROSIS;
D O I
10.7150/thno.50683
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Macrophages are specialized cells that control tissue homeostasis. They include non-resident and tissue-resident macrophage populations which are characterized by the expression of particular cell surface markers and the secretion of molecules with a wide range of biological functions. The differentiation and polarization of macrophages relies on specific growth factors and their receptors. Macrophage-colony stimulating factor (CSF-1) and interleukine-34 (IL-34), also known as "twin" cytokines, are part of this regluatory landscape. CSF-1 and IL-34 share a common receptor, the macrophage-colony stimulating factor receptor (CSF-1R), which is activated in a similar way by both factors and turns on identical signaling pathways. However, there is some discrete differential activation leading to specific activities. In this review, we disscuss recent progress in understanding of the role of the twin cytokines in macrophage differentiation, from their interaction with CSF-1R and the activation of signaling pathways, to their implication in macrophage polarization of non-resident and tissue-resident macrophages. A special focus on IL-34, its involvement in pathophsyiological contexts, and its potential as a theranostic target for macrophage therapy will be proposed.
引用
收藏
页码:1568 / 1593
页数:26
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