{"title":"鼻粘液中的钙网蛋白促进中性粒细胞迁移和病原体清除。","authors":"Yichao Ma, Xinming Qin, Shiqi Liu, Ruoyang Lin, Baoyan Meng, Jian Lin, Qian Yang","doi":"10.1186/s12964-025-02388-5","DOIUrl":null,"url":null,"abstract":"<p><p>The nasal cavity harbors diverse microbiota, and the nasal mucosal innate defense against microbial infiltration is crucial for respiratory infections. Both the nasal mucus covering the surface of the nasal cavity and the neutrophils beneath the nasal epithelia are the first line of innate defense against pathogens. Studying nasal mucus is challenging because of difficulties in collecting stable, high-quality samples from humans. Here, we investigated how nasal mucus cooperates with neutrophils to exert antimicrobial effects. Nasal mucus proteins, derived from nasal mucosal explants of goats, can promote neutrophil migration and increase their bactericidal activity. Calreticulin, identified from total mucus proteins, triggered ICAM-1-dependent transendothelial migration of neutrophils. Moreover, calreticulin activated the Rho GTPases of neutrophils via Toll-like receptor (TLR) 2 to promote their migration and further triggered the release of reactive oxygen species (ROS) and neutrophil extracellular traps (NETs) in a manner dependent on TLR2 and TLR4, accelerating the elimination of pathogens. In vivo studies also demonstrated that nasal inoculation with calreticulin induced neutrophil recruitment to the nasal mucosa and accelerated the clearance of Pasteurella multocida. Together, these findings highlight the synergistic interaction between nasal mucus and neutrophils as an important protective feature in the nasal mucosa.</p>","PeriodicalId":55268,"journal":{"name":"Cell Communication and Signaling","volume":"23 1","pages":"381"},"PeriodicalIF":8.2000,"publicationDate":"2025-08-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12379368/pdf/","citationCount":"0","resultStr":"{\"title\":\"Calreticulin in the nasal mucus promotes neutrophil migration and pathogen clearance.\",\"authors\":\"Yichao Ma, Xinming Qin, Shiqi Liu, Ruoyang Lin, Baoyan Meng, Jian Lin, Qian Yang\",\"doi\":\"10.1186/s12964-025-02388-5\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>The nasal cavity harbors diverse microbiota, and the nasal mucosal innate defense against microbial infiltration is crucial for respiratory infections. Both the nasal mucus covering the surface of the nasal cavity and the neutrophils beneath the nasal epithelia are the first line of innate defense against pathogens. Studying nasal mucus is challenging because of difficulties in collecting stable, high-quality samples from humans. Here, we investigated how nasal mucus cooperates with neutrophils to exert antimicrobial effects. Nasal mucus proteins, derived from nasal mucosal explants of goats, can promote neutrophil migration and increase their bactericidal activity. Calreticulin, identified from total mucus proteins, triggered ICAM-1-dependent transendothelial migration of neutrophils. Moreover, calreticulin activated the Rho GTPases of neutrophils via Toll-like receptor (TLR) 2 to promote their migration and further triggered the release of reactive oxygen species (ROS) and neutrophil extracellular traps (NETs) in a manner dependent on TLR2 and TLR4, accelerating the elimination of pathogens. In vivo studies also demonstrated that nasal inoculation with calreticulin induced neutrophil recruitment to the nasal mucosa and accelerated the clearance of Pasteurella multocida. Together, these findings highlight the synergistic interaction between nasal mucus and neutrophils as an important protective feature in the nasal mucosa.</p>\",\"PeriodicalId\":55268,\"journal\":{\"name\":\"Cell Communication and Signaling\",\"volume\":\"23 1\",\"pages\":\"381\"},\"PeriodicalIF\":8.2000,\"publicationDate\":\"2025-08-26\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12379368/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Cell Communication and Signaling\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1186/s12964-025-02388-5\",\"RegionNum\":2,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CELL BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cell Communication and Signaling","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1186/s12964-025-02388-5","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CELL BIOLOGY","Score":null,"Total":0}
Calreticulin in the nasal mucus promotes neutrophil migration and pathogen clearance.
The nasal cavity harbors diverse microbiota, and the nasal mucosal innate defense against microbial infiltration is crucial for respiratory infections. Both the nasal mucus covering the surface of the nasal cavity and the neutrophils beneath the nasal epithelia are the first line of innate defense against pathogens. Studying nasal mucus is challenging because of difficulties in collecting stable, high-quality samples from humans. Here, we investigated how nasal mucus cooperates with neutrophils to exert antimicrobial effects. Nasal mucus proteins, derived from nasal mucosal explants of goats, can promote neutrophil migration and increase their bactericidal activity. Calreticulin, identified from total mucus proteins, triggered ICAM-1-dependent transendothelial migration of neutrophils. Moreover, calreticulin activated the Rho GTPases of neutrophils via Toll-like receptor (TLR) 2 to promote their migration and further triggered the release of reactive oxygen species (ROS) and neutrophil extracellular traps (NETs) in a manner dependent on TLR2 and TLR4, accelerating the elimination of pathogens. In vivo studies also demonstrated that nasal inoculation with calreticulin induced neutrophil recruitment to the nasal mucosa and accelerated the clearance of Pasteurella multocida. Together, these findings highlight the synergistic interaction between nasal mucus and neutrophils as an important protective feature in the nasal mucosa.
期刊介绍:
Cell Communication and Signaling (CCS) is a peer-reviewed, open-access scientific journal that focuses on cellular signaling pathways in both normal and pathological conditions. It publishes original research, reviews, and commentaries, welcoming studies that utilize molecular, morphological, biochemical, structural, and cell biology approaches. CCS also encourages interdisciplinary work and innovative models, including in silico, in vitro, and in vivo approaches, to facilitate investigations of cell signaling pathways, networks, and behavior.
Starting from January 2019, CCS is proud to announce its affiliation with the International Cell Death Society. The journal now encourages submissions covering all aspects of cell death, including apoptotic and non-apoptotic mechanisms, cell death in model systems, autophagy, clearance of dying cells, and the immunological and pathological consequences of dying cells in the tissue microenvironment.