Mucociliary clearance in cystic fibrosis knockout mice infected with Pseudomonas aeruginosa

被引:16
作者
Cowley, EA
Wang, CG
Gosselin, D
Radzioch, D
Eidelman, DH
机构
[1] ROYAL VICTORIA HOSP, MONTREAL CHEST INST, RES CTR, MEAKINS CHRISTIE LABS, MONTREAL, PQ H3A 1A1, CANADA
[2] MCGILL UNIV, MONTREAL GEN HOSP, CTR HOSP RESISTANCE STUDIES, MONTREAL, PQ H3G 1A4, CANADA
关键词
cystic fibrosis; mice; mucociliary clearance; Pseudomonas aeruginosa;
D O I
10.1183/09031936.97.10102312
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
In this study, we examined whether mucociliary clearance differed between cystic fibrosis (CF) knockout mice and wildtype controls. Additionally, we investigated whether infection with Pseudomonas aeruginosa, a common pathogen in the CF lung, affected this important host defence mechanism, Ciliary beat frequency (feb) and particle transport (PT) were recorded using an in vitro lung explant preparation, Measurements were made from uninfected cystic fibrosis transmembrane conductance regulator (CFTR) knockout (-/-) mice and littermate controls (+/+) and compared to measurements from infected animals, While there were no differences detectable in feb between CFTR -/- mice and their +/+ controls either in the presence or absence of P. aeruginosa, PT rates were different between these groups; interestingly, PT rates appeared dependent on both CFTR and infection status, with uninfected CFTR +/+ animals demonstrating higher rates of PT than their -/- littermates, while CFTR +/+ P. aeruginosa-infected mice demonstrated lower PT than knockout mice, These data demonstrate differences in mucociliary clearance between cystic fibrosis transmembrane conductance regulator knockout mice and controls, and further that Pseudomonas aeruginosa infection affects mucociliary clearance in the peripheral airways of mice, Additionally, the observed differences in particle transport suggest that cystic fibrosis transmembrane conductance regulator knockout mice demonstrate different mucociliary responses to infection.
引用
收藏
页码:2312 / 2318
页数:7
相关论文
共 32 条
[1]  
BOAT TF, 1994, AIRWAY SECRETION PHY, P217
[2]   EPITHELIAL DYSFUNCTION IN CYSTIC-FIBROSIS LUNG-DISEASE [J].
BOUCHER, RC ;
KNOWLES, MR ;
STUTTS, MJ ;
GATZY, JT .
LUNG, 1983, 161 (01) :1-17
[3]  
CASH HA, 1979, AM REV RESPIR DIS, V119, P453
[4]   RELATIONSHIP OF A NON-CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR-MEDIATED CHLORIDE CONDUCTANCE TO ORGAN-LEVEL DISEASE IN CFTR(-/-) MICE [J].
CLARKE, LL ;
GRUBB, BR ;
YANKASKAS, JR ;
COTTON, CU ;
MCKENZIE, A ;
BOUCHER, RC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (02) :479-483
[5]   GENERATION AND CHARACTERIZATION OF A DELTA-F508 CYSTIC-FIBROSIS MOUSE MODEL [J].
COLLEDGE, WH ;
ABELLA, BS ;
SOUTHERN, KW ;
RATCLIFF, R ;
JIANG, CW ;
CHENG, SH ;
MACVINISH, LJ ;
ANDERSON, JR ;
CUTHBERT, AW ;
EVANS, MJ .
NATURE GENETICS, 1995, 10 (04) :445-452
[6]   LUNG-DISEASE IN THE CYSTIC-FIBROSIS MOUSE EXPOSED TO BACTERIAL PATHOGENS [J].
DAVIDSON, DJ ;
DORIN, JR ;
MCLACHLAN, G ;
RANALDI, V ;
LAMB, D ;
DOHERTY, C ;
GOVAN, J ;
PORTEOUS, DJ .
NATURE GENETICS, 1995, 9 (04) :351-357
[7]   CYSTIC-FIBROSIS IN THE MOUSE BY TARGETED INSERTIONAL MUTAGENESIS [J].
DORIN, JR ;
DICKINSON, P ;
ALTON, EWFW ;
SMITH, SN ;
GEDDES, DM ;
STEVENSON, BJ ;
KIMBER, WL ;
FLEMING, S ;
CLARKE, AR ;
HOOPER, ML ;
ANDERSON, L ;
BEDDINGTON, RSP ;
PORTEOUS, DJ .
NATURE, 1992, 359 (6392) :211-215
[8]   INVIVO RETROVIRAL GENE-TRANSFER INTO HUMAN BRONCHIAL EPITHELIA OF XENOGRAFTS [J].
ENGELHARDT, JF ;
YANKASKAS, JR ;
WILSON, JM .
JOURNAL OF CLINICAL INVESTIGATION, 1992, 90 (06) :2598-2607
[9]   MICROBIOLOGY OF AIRWAY DISEASE IN PATIENTS WITH CYSTIC-FIBROSIS [J].
GILLIGAN, PH .
CLINICAL MICROBIOLOGY REVIEWS, 1991, 4 (01) :35-51
[10]   ROLE OF TUMOR-NECROSIS-FACTOR-ALPHA IN INNATE RESISTANCE TO MOUSE PULMONARY INFECTION WITH PSEUDOMONAS-AERUGINOSA [J].
GOSSELIN, D ;
DESANCTIS, J ;
BOULE, M ;
SKAMENE, E ;
MATOUK, C ;
RADZIOCH, D .
INFECTION AND IMMUNITY, 1995, 63 (09) :3272-3278