{"doi":"10.1093/glycob/cwaf071","title":"Layilin at the crossroads of immunity and motility: a C-type lectin receptor in Hyaluronan Signaling","abstract":"Layilin, an understudied C-type lectin receptor for hyaluronan, was initially hypothesized to regulate cell motility due to its binding partner, talin. Subsequent studies identified layilin as a receptor for hyaluronan with roles in regulating cell motility through interactions with key regulatory molecules upstream of cytoskeletal rearrangement: radixin, merlin, focal adhesion kinase (FAK), F-actin, and small GTPases such as RAC1, RAP1, and RhoA. Layilin is also associated with cell-cell interactions, co-localizing with integrins in both T-cells and platelets contributing to epithelial cell junction integrity. Recent studies have found that layilin also plays a role in inflammation, dependent on tissue and disease. In the context of cancer, multiple cancer cell types displaying increased layilin expression contributes to enhanced metastasis. Exhausted CD8+ T cells residing in the tumors exhibit high expression of layilin, with the receptor contributing to increased tissue anchoring and co-expressing with immune checkpoint resistance markers. In other contexts, such as inflammatory bowel disease and atherosclerosis, reduction of layilin results in worsened disease and inflammation. Transcriptomic and epigenetic studies have explored layilin as a prognostic marker, as layilin expression is elevated in multiple cancers, deep vein thrombosis, diabetes, and Alzheimer's. However, the mechanistic role of layilin in most of these studies remains unexplored. This review outlines current insights into Layilin as a molecular hub that links hyaluronan signaling with integrin activity and cytoskeletal dynamics, highlighting its roles in homeostasis, pathogenesis, disease prognosis, and therapeutic intervention across diverse conditions.","journal":"Glycobiology","year":2025,"id":548272,"datarank":0.0,"base_score":0.0,"endowment":0.0,"self_citation_contribution":0.0,"citation_network_contribution":0.0,"self_endowment_contribution":0.0,"citer_contribution":0.0,"corpus_percentile":null,"corpus_rank":null,"citation_count":1,"citer_count":0,"citers_with_citation_signal":0,"citers_with_endowment":0,"datacite_reuse_total":0,"is_dataset":false,"is_dataset_confidence":0.9498,"is_data_producer":false,"deposit_databanks":null,"is_oa":false,"file_count":0,"downloads":0,"has_version_chain":false,"published_date":"2025-01-01","fair_score":null,"fair_percentile":null,"algorithm_id":"datarank_citation_only_1hop_v6","ranking_scope":"data_only","authors":[{"id":105735,"name":"Aaron C. Petrey","orcid":"0000-0002-2696-599X","position":1,"is_corresponding":false},{"id":640242,"name":"Rebecca A. Mellema","orcid":"0000-0003-2769-3153","position":0,"is_corresponding":true}],"reference_count":68,"raw_metadata":null,"created_at":"2026-07-19T02:53:58.530220Z","pmid":"41189332","pmcid":null,"fwci":null,"citation_percentile":null,"influential_citations":0,"oa_status":null,"license":null,"views":0,"total_file_size_bytes":0,"version_count":0,"fair_f":null,"fair_a":null,"fair_i":null,"fair_r":null,"fair_zscore":null,"fair_rationale":null,"fair_model":null,"fair_agent_version":null,"fair_fulltext_source":null,"fair_has_llm":null,"fair_computed_at":null,"clinical_trials":[],"software_tools":[],"db_accessions":[],"linked_datasets":[],"topics":[]}