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

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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.

OriginalsprogEngelsk
Artikelnummer106984
TidsskriftiScience
Vol/bind26
Udgave nummer7
Antal sider21
ISSN2589-0042
DOI
StatusUdgivet - 2023

Bibliografisk note

Funding Information:
This work was supported by the European Commission (GlycoSkin H2020-ERC ), European Commission (Imgene H2020 ), Lundbeck Foundation , The Danish Research Councils (Sapere Aude Research Leader grant to HW), Danish National Research Foundation ( DNRF107 ), The Friis Foundation , The Michelsen Foundation , A.P. Møller og Hustru Chastine Mc-Kinney Møllers Fond til Almene Formaal, Danish Strategic Research Council , Novo Nordisk Foundation ( NNF14CC0001 and NNF17SA0027704 ), and the program of excellence from the University of Copenhagen ( CDO2016 ). HL was supported by a research grant from Galecto Biotech . We are also grateful for excellent technical assistance from Karin Uch Hansen. We acknowledge the Flow Cytometry & Single Cell Core Facility and the Core Facility for Integrated Microscopy, Faculty of Health and Medical Sciences, University of Copenhagen.

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© 2023 The Authors

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