Communications biology · 2026
Mapping galectin-3 ligands in human tear fluid establishes spliceoform-dependent lacritin binding.
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Chang Vincent, Lian Isaac, Mahoney Keira E, Romano Jeffrey, Afshari Ali Reza, Chen Ryan J, Chen Xiangjun, Fineide Fredrik, Khan Ayyad Zartasht, Utheim Tor Paaske, Karlsson Niclas G, Laurie Gordon W, Malaker Stacy A
Аннотация
Galectin-3 (Gal-3) is a carbohydrate-binding protein which plays crucial roles in inflammation, immune response, and cell signaling. At the ocular surface, Gal-3 is also known to crosslink transmembrane mucins to support barrier function. However, the biological role of Gal-3 in circulating tear fluid remains largely unexplored. Similarly, whether Gal-3 engages extracellular glycoprotein ligands in tears to affect biological processes is unknown. Herein, we combine lectin ELISA, affinity enrichment, mass spectrometry (MS)-based glycoproteomics, and lectin blotting to uncover Gal-3 interactors and their associated glycoepitopes. Overall, we report nearly 100 proteins enriched from tear fluid across 3 different patients, identifying proteins involved in immune response, inflammation, and antimicrobial activity. Most notably, we report lacritin as a ligand for Gal-3 and demonstrate that their binding is spliceoform-specific and dependent on lacritin multimerization. Taken together, this study elucidates new ligands for Gal-3 in tear film and investigates new biochemical mechanisms that fine-tune Gal-3 binding events.