Galectin-1 induces a tumor-associated macrophage phenotype and upregulates indoleamine 2,3-dioxygenase-1

被引:15
作者
Rudjord-Levann, Asha M. [1 ]
Ye, Zilu [1 ,2 ]
Hafkenscheid, Lise [1 ]
Horn, Sabrina [1 ]
Wiegertjes, Renske [1 ]
Nielsen, Mathias A. I. [1 ]
Song, Ming [1 ]
Mathiesen, Caroline B. K. [1 ]
Stoop, Jesse [1 ]
Stowell, Sean [3 ]
Straten, Per Thor [4 ]
Leffler, Hakon [5 ]
Vakhrushev, Sergey Y. [1 ]
Dabelsteen, Sally [6 ]
Olsen, Jesper V. [2 ]
Wandall, Hans H. [1 ]
机构
[1] Univ Copenhagen, Fac Hlth & Med Sci, Copenhagen Ctr Glycom, Dept Cellular & Mol Med, Copenhagen, Denmark
[2] Univ Copenhagen, Novo Nordisk Fdn Ctr Prot Res, Fac Hlth & Med Sci, Copenhagen, Denmark
[3] Brigham & Womens Hosp, Dept Pathol, Boston, MA 02115 USA
[4] Copenhagen Univ Hosp, Ctr Canc Immune Therapy, Herlev, Denmark
[5] Div Microbiol Immunol & Glycobiol, BMC C1228b,Klinikgatan 28, Lund, Sweden
[6] Univ Copenhagen, Sch Dent, Dept Oral Med & Pathol, Copenhagen, Denmark
基金
欧盟地平线“2020”; 新加坡国家研究基金会;
关键词
INTERFERON-GAMMA; GENE-EXPRESSION; IFN-GAMMA; FAMILY; CANCER; CELLS; MODULATORS; PHYSIOLOGY; MECHANISM; IMMUNITY;
D O I
10.1016/j.isci.2023.106984
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Galectins are a group of carbohydrate-binding proteins with a presumed immunomodulatory role and an elusive function on antigen-presenting cells. Here we analyzed the expression of galectin-1 and found upregulation of galectin-1 in the extracellular matrix across multiple tumors. Performing an in-depth and dynamic proteomic and phosphoproteomic analysis of human macrophages stimulated with galectin-1, we show that galectin-1 induces a tumor-associated macrophage phenotype with increased expression of key immune checkpoint protein programmed cell death 1 ligand 1 (PD-L1/CD274) and immunomodulator indoleamine 2,3-dioxygenase-1 (IDO1). Galectin-1 induced IDO1 and its active metabolite kynurenine in a dose-dependent manner through JAK/STAT signaling. In a 3D organotypic tissue model system equipped with genetically engineered tumorigenic epithelial cells, we analyzed the cellular source of galectin-1 in the extracellular matrix and found that galectin-1 is derived from epithelial and stromal cells. Our results highlight the potential of targeting galectin-1 in immunotherapeutic treatment of human cancers.
引用
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页数:21
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