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Expression and regulation of PLUNC in human nasal epithelium

Authors
 Chang-Hoon Kim  ;  Kyubo Kim  ;  Hyun Jik Kim  ;  Jin Kook Kim  ;  Jeung-Gweon Lee  ;  Joo-Heon Yoon 
Citation
 Acta Oto-Laryngologica, Vol.126(10) : 1073-1078, 2006 
Journal Title
 Acta Oto-Laryngologica 
ISSN
 0001-6489 
Issue Date
2006
MeSH
Blotting, Western ; Cells, Cultured ; Epithelial Cells/cytology ; Epithelial Cells/drug effects ; Epithelial Cells/metabolism ; Gene Expression Regulation ; Glycoproteins/genetics ; Glycoproteins/isolation & purification* ; Glycoproteins/metabolism* ; Humans ; Immunohistochemistry ; Interleukin-1beta/pharmacology ; Nasal Mucosa/cytology* ; Nasal Mucosa/drug effects ; Nasal Mucosa/metabolism* ; Peptide Fragments/pharmacology ; Phosphoproteins/genetics ; Phosphoproteins/isolation & purification* ; Phosphoproteins/metabolism* ; RNA, Messenger/metabolism ; Reverse Transcriptase Polymerase Chain Reaction ; Tumor Necrosis Factor-alpha/pharmacology ; Turbinates/cytology ; Turbinates/drug effects ; Turbinates/metabolism
Keywords
Secreted protein ; nasal epithelial cells ; PLUNC ; host defense
Abstract
Conclusions. We demonstrated that PLUNC (palate, lung, and nasal epithelium clone) is secreted from nasal epithelial cells and is not influenced by differentiation or proinflammatory mediators. The functional role of PLUNC in the human airway has yet to be elucidated. Objectives. The localization and regulation of PLUNC protein in human nasal epithelium was investigated. First, we located epithelial cells expressing PLUNC protein in human nasal mucosa. Secondly, we sought to identify PLUNC protein in either human nasal secretions from healthy volunteers or apical secretions from cultured human nasal epithelial cells. Lastly, we investigated whether epithelial differentiation and proinflammatory cytokines influence the expression of PLUNC in human nasal epithelial cells. Materials and methods. Immunohistochemical staining for PLUNC was conducted on nasal turbinate specimens. Western blot analysis was conducted on nasal secretions from healthy volunteers, apical secretion from cultured human nasal epithelium, and on normal-appearing posterior ethmoid mucosa, inferior turbinate, and nasal polyp specimens. Reverse transcription-PCR (RT-PCR) of PLUNC was performed with mRNA from cultured human nasal epithelium cells treated with either interleukin-1β or tumor necrosis factor-α. Results. PLUNC was expressed in ciliated cells of surface epithelium and serous cells of the submucosal gland in the human nasal mucosa, and was also found in the nasal secretions of healthy volunteers and apical secretions of cultured human nasal epithelial cells. The degree of mucociliary differentiation and proinflammatory mediators did not influence the expression of PLUNC gene and protein in nasal epithelium.
Full Text
http://informahealthcare.com/doi/abs/10.1080/00016480600606749
DOI
10.1080/00016480600606749
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Otorhinolaryngology (이비인후과학교실) > 1. Journal Papers
Yonsei Authors
Kim, Chang Hoon(김창훈) ORCID logo https://orcid.org/0000-0003-1238-6396
Yoon, Joo Heon(윤주헌)
Lee, Jeung Gweon(이정권)
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/108978
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