Galectin-4 increases the ability of M2 macrophages to enhance antiviral CD4+ T-cell responses

被引:2
作者
Lee, In-Gu [1 ]
Joo, Yong-Hyun [1 ]
Jeon, Hoyeon [1 ]
Jeong, Raehyuk [1 ]
Kim, Eui Ho [2 ]
Chung, Hyunwoo [3 ]
Eyun, Seong-il [1 ]
Kim, Jeongkyu [1 ]
Seo, Young-Jin [1 ]
Hong, So-Hee [4 ]
机构
[1] Chung Ang Univ, Dept Life Sci, 84 Heukseok Ro, Seoul 06974, South Korea
[2] Inst Pasteur Korea, Viral Immunol Lab, 16 Daewangpangyo Ro 712 Beon Gil, Seongnam 13488, South Korea
[3] Natl Inst Allergy & Infect Dis, NIH, Lab Immune Syst Biol, 9000 Rockville Pike, Bethesda, MD 20892 USA
[4] Ewha Womans Univ, Coll Med, Dept Microbiol, 25 Magokdong Ro 2 Gil, Seoul 07804, South Korea
基金
新加坡国家研究基金会;
关键词
galectin-4; M1; macrophage; M2; CD4(+) T cell; lymphocytic choriomeningitis virus; LYMPHOCYTIC CHORIOMENINGITIS VIRUS; IMMUNE-RESPONSES; ACTIVATION; EXPRESSION; DOMAINS; GAMMA; GENE; POLARIZATION; BINDING; LECTIN;
D O I
10.1093/jleuko/qiac008
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Gal-4 enhances the immunostimulatory activity of M2 macrophages upon viral infection, leading to the reinforced antiviral functionality of CD4(+) T cells. Galectin-4 (Gal-4) is a beta-galactoside-binding protein belonging to the galectin family. Although Gal-4 is known to be involved in several physiologic processes of the gastrointestinal tract, its immunomodulatory roles remain unclear. In this study, we investigated whether Gal-4 influences the function of M1 and M2 macrophages. Gal-4 treatment drove more robust changes in the gene expression of M2 macrophages compared to M1 macrophages. Antiviral immune response-related genes were significantly upregulated in Gal-4-treated M2 macrophages. Gal-4 significantly enhanced the immunostimulatory activity of M2 macrophages upon Toll-like receptor 7 stimulation or infection with lymphocytic choriomeningitis virus (LCMV). Moreover, the antibody production against LCMV infection and the antiviral CD4(+) T-cell responses, but not the antiviral CD8(+) T-cell responses, were greatly increased by Gal-4-treated M2 macrophages in vivo. The present results indicate that Gal-4 enhances the ability of M2 macrophages to promote antiviral CD4(+) T-cell responses. Thus, Gal-4 could be used to boost antiviral immune responses.
引用
收藏
页码:71 / 83
页数:13
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