Difference in Chemokine Expression in Airway Epithelial Cells According to the Virulence of Tubercle Bacilli.
10.4046/trd.1997.44.4.729
- Author:
O Jung KWON
;
Hojoong KIM
;
Jung Hee KIM
;
Ho Cheol KIM
;
Gee Young SUH
;
Jeong Woong PARK
;
Sang Joon PARK
;
Man Pyo CHUNG
;
Dong Chull CHOI
;
Chong H RHEE
- Publication Type:Original Article
- Keywords:
Tuberculosis;
Chemokine;
Airway epithelial cells;
Virulence
- MeSH:
Blotting, Northern;
Chemokine CCL5;
Chemokines;
Enzyme-Linked Immunosorbent Assay;
Epithelial Cells*;
Healthy Volunteers;
Interleukin-8;
Monocytes;
Phagocytosis;
RNA, Messenger;
Tuberculosis;
Tuberculosis, Pulmonary;
Tumor Necrosis Factor-alpha;
Virulence*
- From:Tuberculosis and Respiratory Diseases
1997;44(4):729-741
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
BACKGROUND: We have recently reported that airway epithelial cells can produce RANTES and IL-8 in response to the stimulation of tubercle bacilli wuggesting a certain role of airway epithelial cells in the pathogenesis of pulmonary tuberculosis. The pathogenesis of tuberculosis is determined by several factors including phagocytosis, immunological response of host, and virulence of tubercle bacilli. Interestingly, there have been reports suggesting that difference in immunological response of host according to the virulence of tubercle bacilli may be related with the pathogenesis of tuberculosis. We, therfore, studied the expressions and productions of RANTES and IL-8 in airway epithelial cells in response to tubercle bacilli(H37Rv, virulent strain and H37Ra, avirulent strain), in order to elucidate the possible pathophysiology of pulmonary tuberculosis. METHODS: Peripheral blood monocytes were isolated from normal volunteers. Peripheral blood monocytes(OBM) were stimulated with LPS(10 micrograms/ml), H37Rv, or H37Ra(5X10(5) bacilli/well) along with normal control for 24 hours. A549 cells were stimulated with supernatants of cultured PBM for 24 hours. ELISA kit was used for the measurement of TNFalpha and IL-1beta production in supernatants of cultured PBM and for the measurement of RANTES and IL-8 in supernatants of cultured A549 cells. Northern blot analysis was used for the measurement of RANTES and IL-8 mRNA expression in cultured A549 cells. RESULTS: TNFalpha and IL-1beta productions were increased in cultured PBM stimulated with LPS or tubercle bacilli(H37Rv or H37Ra) compared with the control. There was, however, no difference in TNFalpha and IL-1beta production between cultured PBM stimulated with H37Rv and H37Ra. RANTES and IL-8 expressions and productions were also increased in cultured A549 cells stimulated with LPS or tubercle bacilli compared with the control. RANTES and IL-8 mRNA expressions were significantly increased in cultured A549 cells stimulated with H37Ra-conditioned media(CM) compared with A549 cells stimulated with H37Rv-CM (p<0.05). However, there was no difference in RANTES and IL-8 productions between A549 cells stimulated with H37Rv-CM and H37Ra-CM. CONCLUSION: Airway epithelial cells can produce the potent chemokines such as RANTES and IL-8, in response to the stimulation of tubercle bacilli. These results suggest that airway epithelial cells may play a certain role in the pathogenesis of pulmonary tuberculosis. However, the role of airway epithelial cells in the pathogenesis of tuberculosis according to the virulence of tubercle bacilli was not clear in this study.
