Cystic fibrosis airway epithelial cell polarity and bacterial flagellin determine host response to Pseudomonas aeruginosa

被引:66
作者
Hybiske, K
Ichikawa, JK
Huang, V
Lory, SJ
Machen, TE
机构
[1] Univ Calif Berkeley, Dept Mol & Cell Biol, Berkeley, CA 94720 USA
[2] Harvard Univ, Sch Med, Dept Microbiol & Mol Genet, Boston, MA 02130 USA
关键词
D O I
10.1046/j.1462-5822.2003.00342.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The role of epithelial polarity and bacterial factors in the control of the innate immune response of airway epithelial cells to Pseudomonas aeruginosa PAK was investigated using a human, nasal cystic fibrosis (DeltaF508/DeltaF508) epithelial cell line CF15 grown as confluent layers on permeable supports. Addition of PAK to the basal surface of CF15 layers caused significant expression changes in 1525 different genes (out of 12 625 examined), including the cytokines IL-6, IL-8, IL-1beta and TNF-alpha, as well as genes associated with leucocyte adhesion, antibacterial factors, and NF-kappaB signalling. Confocal microscopy showed that nuclear migration of NF-kappaB in all CF15 cells was preceded by PAK binding to the basal and lateral surfaces of some cells. Addition of PAK to the apical surface of CF15 monolayers elicited changes in expression of only 602 genes, including 256 not affected during basolateral PAK exposure. Over time, cytokine expression during apical PAK was similar to that exhibited by basal PAK, but the magnitudes during apical treatment were much smaller with little/no nuclear migration of NF-kappaB in CF15 cells. Furthermore, these responses depended on the presence of flagellin, but not pili on the bacteria. Thus, P. aeruginosa triggered a strong innate immune response that depended on the apical versus basolateral polarity of CF15 cells and the presence of flagellin on the bacteria.
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页码:49 / 63
页数:15
相关论文
共 44 条
[1]   Inflammatory response in airway epithelial cells isolated from patients with cystic fibrosis [J].
Aldallal, N ;
McNaughton, EE ;
Manzel, LJ ;
Richards, AM ;
Zabner, J ;
Ferkol, TW ;
Look, DC .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2002, 166 (09) :1248-1256
[2]   CHARACTERIZATION OF PSEUDOMONAS-AERUGINOSA-INDUCED MDCK CELL INJURY - GLYCOSYLATION-DEFECTIVE HOST-CELLS ARE RESISTANT TO BACTERIAL KILLING [J].
APODACA, G ;
BOMSEL, M ;
LINDSTEDT, R ;
ENGEL, J ;
FRANK, D ;
MOSTOV, KE ;
WIENERKRONISH, J .
INFECTION AND IMMUNITY, 1995, 63 (04) :1541-1551
[3]   Stereotyped and specific gene expression programs in human innate immune responses to bacteria [J].
Boldrick, JC ;
Alizadeh, AA ;
Diehn, M ;
Dudoit, S ;
Liu, CL ;
Belcher, CE ;
Botstein, D ;
Staudt, LM ;
Brown, PO ;
Relman, DA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (02) :972-977
[4]   Altered respiratory epithelial cell cytokine production in cystic fibrosis [J].
Bonfield, TL ;
Konstan, MW ;
Berger, M .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 1999, 104 (01) :72-78
[5]   EVIDENCE FOR REDUCED CL- AND INCREASED NA+ PERMEABILITY IN CYSTIC-FIBROSIS HUMAN PRIMARY-CELL CULTURES [J].
BOUCHER, RC ;
COTTON, CU ;
GATZY, JT ;
KNOWLES, MR ;
YANKASKAS, JR .
JOURNAL OF PHYSIOLOGY-LONDON, 1988, 405 :77-103
[6]   Heterogeneous transcription of an indoleacetic acid biosynthetic gene in Erwinia herbicola on plant surfaces [J].
Brandl, MT ;
Quiñones, B ;
Lindow, SE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (06) :3454-3459
[7]  
CRYSTAL RG, 1991, LUNG SCI FDN, P527
[8]   Host microarray analysis reveals a role for the Salmonella response regulator phoP in human macrophage cell death [J].
Detweiler, CS ;
Cunanan, DB ;
Falkow, S .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (10) :5850-5855
[9]   DIVERSE PSEUDOMONAS-AERUGINOSA GENE-PRODUCTS STIMULATE RESPIRATORY EPITHELIAL-CELLS TO PRODUCE INTERLEUKIN-8 [J].
DIMANGO, E ;
ZAR, HJ ;
BRYAN, R ;
PRINCE, A .
JOURNAL OF CLINICAL INVESTIGATION, 1995, 96 (05) :2204-2210
[10]   Activation of NF-κB by adherent Pseudomonas aeruginosa in normal and cystic fibrosis respiratory epithelial cells [J].
DiMango, E ;
Ratner, AJ ;
Bryan, R ;
Tabibi, S ;
Prince, A .
JOURNAL OF CLINICAL INVESTIGATION, 1998, 101 (11) :2598-2605