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http://purl.uniprot.org/citations/31825941http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/31825941http://www.w3.org/2000/01/rdf-schema#comment"

Introduction

Chronic rhinosinusitis (CRS) is a local inflammation of the nasal mucosa and sinus that persists for >12 weeks. As CC chemokine ligand (CCL) 19 expression is known to be elevated in CRS, and CCL 19, CCL21, and CCL25 share the same atypical chemokine receptor 4, so we focused on CCL21 and CCL25.

Objectives

To investigate the expression of CCL21 and CCL25 in different types of CRS and their significance in CRS development.

Methods

A total of 116 patients participated in the study, and uncinate process mucosa or nasal polyp (NP) specimens were collected during surgery. Western blotting and immunohistochemistry were performed to detect the expression of CCL21 and CCL25, respectively, in the nasal mucosa. Immunofluorescence was used to determine their cellular localization in NPs, whereas macrophage culture was used to determine their relationships with macrophages.

Results

Immunohistochemistry revealed that the expressions of CCL21 and CCL25 were increased in NPs only. Western blotting revealed that these expressions were gradually increased in control, CRS without NP and CRS with NP groups and were positively correlated with disease severity. Furthermore, increased expressions of CCL21 and CCL25 in NPs were not related to eosinophil infiltration. Immunofluorescence results demonstrated colocalization of CCL25+ cells and CD68+ macrophages. CCL25 expression was increased in macrophage culture, especially in M1 macrophages, while CCL21 expression was not significantly associated with macrophages.

Conclusions

CCL21 and CCL25 were significantly upregulated in NPs and positively correlated with disease severity. CCL25 upregulation was related to M1 macrophages."xsd:string
http://purl.uniprot.org/citations/31825941http://purl.org/dc/terms/identifier"doi:10.1159/000504476"xsd:string
http://purl.uniprot.org/citations/31825941http://purl.uniprot.org/core/author"Li F."xsd:string
http://purl.uniprot.org/citations/31825941http://purl.uniprot.org/core/author"Xu Y."xsd:string
http://purl.uniprot.org/citations/31825941http://purl.uniprot.org/core/author"Deng Y.Q."xsd:string
http://purl.uniprot.org/citations/31825941http://purl.uniprot.org/core/author"Chen S.M."xsd:string
http://purl.uniprot.org/citations/31825941http://purl.uniprot.org/core/author"Liu M.Z."xsd:string
http://purl.uniprot.org/citations/31825941http://purl.uniprot.org/core/author"Tao Z.Z."xsd:string
http://purl.uniprot.org/citations/31825941http://purl.uniprot.org/core/author"Kong Y.G."xsd:string
http://purl.uniprot.org/citations/31825941http://purl.uniprot.org/core/date"2020"xsd:gYear
http://purl.uniprot.org/citations/31825941http://purl.uniprot.org/core/name"Int Arch Allergy Immunol"xsd:string
http://purl.uniprot.org/citations/31825941http://purl.uniprot.org/core/pages"159-169"xsd:string
http://purl.uniprot.org/citations/31825941http://purl.uniprot.org/core/title"Increased Expressions and Roles of CC Chemokine Ligand 21 and CC Chemokine Ligand 25 in Chronic Rhinosinusitis with Nasal Polyps."xsd:string
http://purl.uniprot.org/citations/31825941http://purl.uniprot.org/core/volume"181"xsd:string
http://purl.uniprot.org/citations/31825941http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/31825941
http://purl.uniprot.org/citations/31825941http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/31825941
http://purl.uniprot.org/uniprot/#_O00585-mappedCitation-31825941http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/31825941
http://purl.uniprot.org/uniprot/O00585http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/31825941