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1 Department of Geriatric and Respiratory Medicine, Tohoku University School of Medicine, Sendai 980-8574; 3 Virus Center, Clinical Research Division, Sendai National Hospital, Sendai 983-0045; and 2 Department of Pulmonary Medicine, Institute of Clinical Medicine, University of Tsukuba, Tsukuba 305-8575, Japan
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-
B (NF-
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
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