Erratum: Non-invasive airway health assessment: Synchrotron imaging reveals effects of rehydrating treatments on mucociliary transit in-vivo (Scientific Reports 4:3689 DOI: 10.1038/srep03689);Non-invasive airway health assessment: Synchrotron imaging reveals effects of rehydrating treatments on mucociliary transit in-vivo

Scientific Reports

Volumn 4, Issue , 2014, Pages

  Donnelley, Martin ^a,b,c   Morgan, Kaye S ^d   Siu, Karen K W ^d,e   Farrow, Nigel R ^a,b,c   Stahr, Charlene S ^d   Boucher, Richard C ^f   Fouras, Andreas ^d   Parsons, David W ^a,b,c  

^a WOMEN S AND CHILDREN S HOSPITAL   (Australia)

^b UNIVERSITY OF ADELAIDE   (Australia)

^c UNIVERSITY OF ADELAIDE   (Australia)

^d MONASH UNIVERSITY   (Australia)

^e AUSTRALIAN SYNCHROTRON   (Australia)

^f UNIVERSITY OF NORTH CAROLINA SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

SODIUM CHLORIDE;

ANIMAL; C57BL MOUSE; CYSTIC FIBROSIS; DIAGNOSTIC IMAGING; MOUSE; PARTICLE SIZE; PROCEDURES; RESPIRATORY SYSTEM; SCINTISCANNING; SYNCHROTRON; X RAY;

ANIMALS; CYSTIC FIBROSIS; DIAGNOSTIC IMAGING; MICE; MICE, INBRED C57BL; PARTICLE SIZE; RESPIRATORY SYSTEM; SALINE SOLUTION, HYPERTONIC; SYNCHROTRONS; X-RAYS;

EID: 84903577923     PISSN: None     EISSN: 20452322     Source Type: Journal    
DOI: 10.1038/srep05361     Document Type: Erratum

References (28)

1. Boucher, R. C. New concepts of the pathogenesis of cystic fibrosis lung disease. Eur Respir J 23, 146-158, doi:10.1183/09031936.03.00057003 (2004).
2. Stocker, A. et al. Single-dose lentiviral gene transfer for lifetime airway gene expression. J Gene Med 11, 861-867, doi:10.1002/jgm.1368 (2009).
3. Limberis, M., Anson, D. S., Fuller, M. & Parsons, D. W. Recovery of airway cystic fibrosis transmembrane conductance regulator function in mice with cystic fibrosis after single-dose lentivirus-mediated gene transfer. Hum Gene Ther 13, 2112-2112, doi:10.1089/10430340260355365 (2002).
4. Donnelley, M., Morgan, K., Siu, K. K. W. & Parsons, D. W. Dry deposition of pollutant and marker particles onto live mouse airway surfaces enhances monitoring of individual particle mucociliary transit behaviour. J Synchrotron Radiat 19, 551-558, doi:10.1107/S0909049512018250 (2012).
5. Donnelley, M. et al. A new technique to examine individual particle and fibre deposition and transit behaviour on live mouse trachea. J Synchrotron Radiat 17, 719-729, doi:10.1107/S0909049510028451 (2010).
6. Donnelley, M. et al. Real-time non-invasive detection of inhalable particulates delivered into live mouse airways. 16, 553-561, doi:10.1107/S0909049509012618 (2009).
7. Grubb, B. R., Jones, J. H. & Boucher, R. C. Mucociliary transport determined by in vivo microdialysis in the airways of normal and CF mice. Am J Physiol Lung Cell Mol Physiol 286, L588-595, doi:10.1152/ajplung.00302.2003 (2004).
8. Donaldson, S. H., Corcoran, T. E., Laube, B. L. & Bennett, W. D. Mucociliary clearance as an outcome measure for cystic fibrosis clinical research. Proc Am Thorac Soc 4, 399-405, doi:10.1513/pats.200703-042BR (2007).
9. Livraghi, A. & Randell, S. H. Cystic fibrosis and other respiratory diseases of impaired mucus clearance. Toxicologic pathology 35, 116-129, doi:10.1080/ 01926230601060025 (2007).
10. Hua, X. Y. et al. Noninvasive real-time measurement of nasal mucociliary clearance in mice by pinhole gamma scintigraphy. J Appl Physiol 108, 189-196, doi:10.1152/japplphysiol.00669.2009 (2010).
11. Cooper, J. L., Quinton, P. M. & Ballard, S. T. Mucociliary transport in porcine trachea: Differential effects of inhibiting chloride and bicarbonate secretion. Am J Physiol Lung C 304, L184-L190, doi:10.1152/ajplung.00143.2012 (2013).
12. Ballard, S. T., Parker, J. C. & Hamm, C. R. Restoration of mucociliary transport in the fluid-depleted trachea by surface-active instillates. Am J Resp Cell Mol 34, 500-504, doi:10.1165/rcmb.2005-0214OC (2006).
13. Snigirev, A., Snigireva, I., Kohn, V., Kuznetsov, S. & Schelokov, I. On the possibilities of x-ray phase contrast microimaging by coherent high-energy synchrotron radiation. Rev Sci Instrum 66, 5486-5492, doi:10.1063/1.1146073 (1995).
14. Cloetens, P., Barrett, R., Baruchel, J., Guigay, J. P. & Schlenker, M. Phase objects in synchrotron radiation hard X-ray imaging. J Phys D Appl Phys 29, 133-146, doi:10.1088/0022-3727/29/1/023 (1996).
15. Wilkins, S. W., Gureyev, T. E., Gao, D., Pogany, A. & Stevenson, A. W. Phasecontrast imaging using polychromatic hard X-rays. Nature 384, 335-338, doi:10.1038/384335a0 (1996).
16. Parsons, D. W. et al. High-resolution visualization of airspace structures in intact mice via synchrotron phase-contrast X-ray imaging (PCXI). J Anat 213, 217-227, doi:10.1111/j.1469-7580.2008.00950.x (2008).
17. Siu, K. K.W. et al. Phase contrast X-ray imaging for the non-invasive detection of airway surfaces and lumen characteristics in mouse models of airway disease. Eur J Radiol 68, S22-S26, doi:10.1016/j.ejrad.2008.04.029 (2008).
18. Donnelley, M., Morgan, K., Siu, K. & Parsons, D. Variability of in vivo fluid dose distribution in mouse airways is visualized by high-speed synchrotron x-ray imaging. J Aerosol Med Pulm D 26, 1-10, doi:10.1089/jamp.2012.1007 (2012).
19. Donnelley, M., Siu, K., Jamison, A. & Parsons, D. Synchrotron phase contrast Xray imaging reveals fluid dosing dynamics in mouse airways. Gene Ther 19, 8-14, doi:10.1038/gt.2011.80 (2012).
20. Robinson, M. et al. Effect of increasing doses of hypertonic saline on mucociliary clearance in patients with cystic fibrosis. Thorax 52, 900-903, doi:10.1136/ thx.52.10.900 (1997).
21. Button, B., Okada, S. F., Frederick, C. B., Thelin, W. R. & Boucher, R. C. Mechanosensitive ATP release maintains proper mucus hydration of airways. Science signaling 6, ra46, doi:10.1126/scisignal.2003755 (2013).
22. Tarran, R., Trout, L., Donaldson, S. H. & Boucher, R. C. Soluble mediators, not cilia, determine airway surface liquid volume in normal and cystic fibrosis superficial airway epithelia. The Journal of general physiology 127, 591-604, doi:10.1085/jgp.200509468 (2006).
23. Donaldson, S. H. et al. Mucus clearance and lung function in cystic fibrosis with hypertonic saline. New Engl J Med 354, 241-250, doi:10.1056/Nejmoa043891 (2006).
24. Hirsh, A. J. et al. Pharmacological properties of N-(3,5-diamino-6-chloropyrazine-2-carbonyl)-N ?-4-[4-(2,3-dihydroxypropoxy)phenyl]butylguanidine methanesulfonate (552-02), a novel epithelial sodium channel blocker with potential clinical efficacy for cystic fibrosis lung disease. J Pharmacol Exp Ther 325, 77-88, doi:10.1124/jpet.107.130443 (2008).
25. JL, G. & B, B. An In Vitro Study of the Kinetics of Hypertonic Saline on ASL Height. Pediatr Pulm 45:S33, 291.
26. Yabashi, M. et al. SPring-8 standard x-ray monochromators. Proc. SPIE 3773, 2-13, doi:10.1117/12.370098 (1999).
27. Donnelley, M., Parsons, D., Morgan, K. & Siu, K. Animals In Synchrotrons: Overcoming Challenges For High-Resolution, Live, Small-Animal Imaging. AIP Conf Proc 1266, doi:10.1063/1.3478192 (2010).
28. Hamacher, J. et al. Microscopic wire guide-based orotracheal mouse intubation: Description, evaluation and comparison with transillumination. Lab Anim 42, 222-230, doi:10.1258/la.2007.006068 (2008).