TY - JOUR
T1 - Persistent depletion of I kappa B alpha and interleukin-8 expression in human pulmonary epithelial cells exposed to quartz particles
AU - Schins, Roel P.F.
AU - McAlinden, Audrey
AU - MacNee, William
AU - Jimenez, L. Albert
AU - Ross, James A.
AU - Guy, Keith
AU - Faux, Stephen P.
AU - Donaldson, Ken
N1 - Funding Information:
This study was supported by a grant from the Colt Foundation. K.D. is a Transco British Lung Foundation Fellow in Air Pollution and Respiratory Health.
PY - 2000
Y1 - 2000
N2 - Chronic inflammation and fibrosis following quartz inhalation has been associated with persistent up-regulation of several 'pro-inflammatory' genes, which are commonly regulated by nuclear factor kappa-B (NF-κB). Transcription of the NF-κB-inhibitor IκBα is also under NF-κB control, and its de novo synthesis is considered to comprise a negative feedback loop in transient inflammation. To investigate this mechanism in particle inflammation, we have studied IκBα degradation in A549 cells exposed to DQ12-quartz or TiO2, in relation to the expression of IL-8. Although both quartz and TiO2 were found to cause IκBα degradation, only quartz elicited a mild IκBα depletion, first appearing at 4 h. TiO2 was found to cause a higher short-term increase in IκBα mRNA-expression compared to quartz, whereas the early enhancement of IL-8 expression and release was similar for both particles. Up-regulation of IL-8 expression was found to persist with quartz only. Cotreatment with PDTC and curcumin reduced particle-elicited IL-8 response, whereas cycloheximide caused enhancement of IL-8 mRNA expression in both the quartz- and TiO2-treated cells. Our results demonstrate that mineral dusts cause IκBα degradation, a transient increase in de novo synthesis of IκBα, and enhanced IL-8 expression in human pulmonary epithelial cells. While IκBα degradation and early IL-8 expression seem to be general particle phenomena, particle-specific characteristics impact on activation of IκBα gene transcription, apparently accounting for the different proinflammatory IL-8 responses seen with quartz and TiO2 in the longer term. These observations may provide an explanation for the transient versus the persistent pulmonary inflammatory status and subsequent differences in pathogenic potency of TiO2 and quartz. (C) 2000 Academic Press.
AB - Chronic inflammation and fibrosis following quartz inhalation has been associated with persistent up-regulation of several 'pro-inflammatory' genes, which are commonly regulated by nuclear factor kappa-B (NF-κB). Transcription of the NF-κB-inhibitor IκBα is also under NF-κB control, and its de novo synthesis is considered to comprise a negative feedback loop in transient inflammation. To investigate this mechanism in particle inflammation, we have studied IκBα degradation in A549 cells exposed to DQ12-quartz or TiO2, in relation to the expression of IL-8. Although both quartz and TiO2 were found to cause IκBα degradation, only quartz elicited a mild IκBα depletion, first appearing at 4 h. TiO2 was found to cause a higher short-term increase in IκBα mRNA-expression compared to quartz, whereas the early enhancement of IL-8 expression and release was similar for both particles. Up-regulation of IL-8 expression was found to persist with quartz only. Cotreatment with PDTC and curcumin reduced particle-elicited IL-8 response, whereas cycloheximide caused enhancement of IL-8 mRNA expression in both the quartz- and TiO2-treated cells. Our results demonstrate that mineral dusts cause IκBα degradation, a transient increase in de novo synthesis of IκBα, and enhanced IL-8 expression in human pulmonary epithelial cells. While IκBα degradation and early IL-8 expression seem to be general particle phenomena, particle-specific characteristics impact on activation of IκBα gene transcription, apparently accounting for the different proinflammatory IL-8 responses seen with quartz and TiO2 in the longer term. These observations may provide an explanation for the transient versus the persistent pulmonary inflammatory status and subsequent differences in pathogenic potency of TiO2 and quartz. (C) 2000 Academic Press.
UR - http://www.scopus.com/inward/record.url?scp=0034283409&partnerID=8YFLogxK
U2 - 10.1006/taap.2000.8982
DO - 10.1006/taap.2000.8982
M3 - Article
C2 - 10964761
AN - SCOPUS:0034283409
SN - 0041-008X
VL - 167
SP - 107
EP - 117
JO - Toxicology and Applied Pharmacology
JF - Toxicology and Applied Pharmacology
IS - 2
ER -