Literature DB >> 15454780

mRNA for genes associated with antigen presentation are expressed by human middle meatal epithelial cells in culture.

Andrew P Lane1, Bahman Saatian, Xiao-Ying Yu, Ernst William Spannhake.   

Abstract

OBJECTIVES/HYPOTHESIS: Although the mechanisms underlying the initiation and maintenance of inflammation in chronic rhinosinusitis are poorly understood, the activation of memory T cells within the nasal mucosa is thought to play an important role. T-cell activation requires specialized antigen processing and presentation of antigen by immunocompetent cells in the context of cell surface immune molecules. The purpose of this study was to investigate the expression of such molecules by human sinonasal epithelial cells grown in culture at the air-liquid interface (ALI).
METHODS: Middle meatal epithelium was obtained from six patients undergoing endoscopic sinus surgery. Dissociated epithelial cells were grown to confluence in serum-free, defined medium and transferred to filter inserts for culture at the ALI. Cells were harvested at 2 and 21 days of growth at the ALI and processed for real-time polymerase chain reaction (PCR). The presence and relative abundance of constitutively expressed mRNA for human leukocyte antigen (HLA)-B, HLA-DR, B7 to 1, B7 to 2, B7-H2, B7-H3, and cathepsin D were assessed.
RESULTS: After 2 days at the ALI, middle meatal epithelial cells demonstrated expression of genes for each of the antigen processing associated genes tested. The expression of HLA-B and HLA-DR increased significantly with cellular maturation at the ALI. Expression of HLA-DR and B7 to 1 increased with cytokine stimulation.
CONCLUSIONS: Primary human epithelial cells obtained from the middle meatus express genes associated with antigen presentation function. The pattern of gene expression is modulated by cytokine stimulation and changes as the cells differentiate at the ALI. These findings suggest that mature middle meatal epithelial cells have the cellular machinery to interact with T cells and therefore may be direct participants in the modulation of T-cell activity in chronic sinusitis.

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Year:  2004        PMID: 15454780     DOI: 10.1097/00005537-200410000-00028

Source DB:  PubMed          Journal:  Laryngoscope        ISSN: 0023-852X            Impact factor:   3.325


  12 in total

1.  Chitin stimulates expression of acidic mammalian chitinase and eotaxin-3 by human sinonasal epithelial cells in vitro.

Authors:  Ashley Lalaker; Louis Nkrumah; Won-Kyung Lee; Murugappan Ramanathan; Andrew P Lane
Journal:  Am J Rhinol Allergy       Date:  2009 Jan-Feb       Impact factor: 2.467

2.  The role of hepatocyte growth factor/c-Met in chronic rhinosinusitis with nasal polyps.

Authors:  Douglas D Reh; Murugappan Ramanathan; Babar Sultan; Yadong Wang; Lindsey May; Andrew P Lane
Journal:  Am J Rhinol Allergy       Date:  2010 Jul-Aug       Impact factor: 2.467

3.  Amalgam tattoo: a cause of sinusitis?

Authors:  José Luiz Santos Parizi; Gisele Alborghetti Nai
Journal:  J Appl Oral Sci       Date:  2010 Jan-Feb       Impact factor: 2.698

4.  Influenza A Virus M2 Protein Apical Targeting Is Required for Efficient Virus Replication.

Authors:  Nicholas Wohlgemuth; Andrew P Lane; Andrew Pekosz
Journal:  J Virol       Date:  2018-10-29       Impact factor: 5.103

5.  Immunoglobulins in nasal secretions of patients with allergic rhinitis and chronic rhinosinusitis.

Authors:  Chung-Han Hsin; Chia-Tung Shun; Chia-Ming Liu
Journal:  Eur Arch Otorhinolaryngol       Date:  2007-11-08       Impact factor: 2.503

Review 6.  Technical advances in rhinologic basic science research.

Authors:  Murugappan Ramanathan; Justin H Turner; Andrew P Lane
Journal:  Otolaryngol Clin North Am       Date:  2009-10       Impact factor: 3.346

7.  Th2 cytokines associated with chronic rhinosinusitis with polyps down-regulate the antimicrobial immune function of human sinonasal epithelial cells.

Authors:  Murugappan Ramanathan; Won-Kyung Lee; Ernst W Spannhake; Andrew P Lane
Journal:  Am J Rhinol       Date:  2008 Mar-Apr

8.  The M2 protein of live, attenuated influenza vaccine encodes a mutation that reduces replication in human nasal epithelial cells.

Authors:  Nicholas Wohlgemuth; Yang Ye; Katherine J Fenstermacher; Hsuan Liu; Andrew P Lane; Andrew Pekosz
Journal:  Vaccine       Date:  2017-10-25       Impact factor: 3.641

9.  Sinonasal epithelial wound resealing in an in vitro model: inhibition of wound closure with IL-4 exposure.

Authors:  Sarah K Wise; Kyle A Den Beste; Elizabeth K Hoddeson; Charles A Parkos; Asma Nusrat
Journal:  Int Forum Allergy Rhinol       Date:  2013-03-06       Impact factor: 3.858

10.  Evaluation of the innate immune responses to influenza and live-attenuated influenza vaccine infection in primary differentiated human nasal epithelial cells.

Authors:  Adriana Forero; Katherine Fenstermacher; Nicholas Wohlgemuth; Andrew Nishida; Victoria Carter; Elise A Smith; Xinxia Peng; Melissa Hayes; Doreen Francis; John Treanor; Juliet Morrison; Sabra L Klein; Andrew Lane; Michael G Katze; Andrew Pekosz
Journal:  Vaccine       Date:  2017-09-28       Impact factor: 3.641

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