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Type 2 rhinovirus infection of cultured human tracheal epithelial cells: role of LDL receptor

Authors :
SUZUKI, TOMOKO
YAMAYA, MUTSUO
KAMANAKA, MASAHITO
JIA, YU X.
NAKAYAMA, KATSUTOSHI
HOSODA, MASAYOSHI
YAMADA, NORIHIRO
NISHIMURA, HIDEKAZU
SEKIZAWA, KIYOHISA
SASAKI, HIDETADA
Source :
The American Journal of Physiology. March, 2001, Vol. 280 Issue 3, L409
Publication Year :
2001

Abstract

Suzuki, Tomoko, Mutsuo Yamaya, Masahito Kamanaka, Yu X. Jia, Katsutoshi Nakayama, Masayoshi Hosoda, Norihiro Yamada, Hidekazu Nishimura, Kiyohisa Sekizawa, and Hidetada Sasaki. Type 2 rhinovirus infection of cultured human tracheal epithelial cells: role of LDL receptor. Am J Physiol Lung Cell Mol Physiol 280: L409-L420, 2001.--To examine the role of the low-density lipoprotein (LDL) receptor on minor group human rhinovirus (RV) infection, primary cultures of human tracheal epithelial cells were infected with a minor group (RV2) or a major group (RV14) RV. Viral infection was confirmed by showing with PCR that viral titers in supernatants and lysates from infected cells increased with time. RV2 and RV14 increased expression of mRNA and protein of the LDL receptor on the cells and the cytokine production. RV2 induced activation of transcription factors SP1 and nuclear factor-[Kappa]B (NF-[Kappa]B). An antibody to the LDL receptor inhibited RV2 infection and RV2-induced cytokine production without an effect on RV14 infection and RV14-induced cytokine production. These findings imply that RV2 upregulates LDL receptor expression on airway epithelial cells, thereby increasing susceptibility to minor group RV infection. LDL receptor expression and cytokine production may be mediated, in part, via activation of transcription factors by RV2. These events may be important in airway inflammation after minor group RV infection in asthma. asthma; common cold; airway inflammation; low-density lipoprotein receptor

Details

ISSN :
00029513
Volume :
280
Issue :
3
Database :
Gale General OneFile
Journal :
The American Journal of Physiology
Publication Type :
Academic Journal
Accession number :
edsgcl.72268855