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ORIGINAL ARTICLE

Determinants of culture success in an airway epithelium sampling program of young children with cystic fibrosis

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Pages 447-459 | Received 24 Mar 2014, Accepted 16 Jul 2014, Published online: 05 Sep 2014

REFERENCES

  • Welsh MJ, Smith AE. Molecular mechanisms of CFTR chloride channel dysfunction in cystic fibrosis. Cell. 1993 Jul 2;73(7):1251–1254.
  • Mehta A. CFTR: more than just a chloride channel. Pediatr Pulmonol. 2005 Apr;39(4):292–298.
  • Borowitz D, Baker RD, Stallings V. Consensus report on nutrition for pediatric patients with cystic fibrosis. J Pediatr Gastroenterol Nutr. 2002 Sep;35(3):246–259.
  • Tiddens HA, Koopman LP, Lambert RK, Elliott WM, Hop WC, van der Mark TW, de Boer WJ, de Jongste JC. Cartilaginous airway wall dimensions and airway resistance in cystic fibrosis lungs. Eur Respir J. 2000 Apr;15(4):735–742.
  • Lyczak JB, Cannon CL, Pier GB. Lung infections associated with cystic fibrosis. Clin Microbiol Rev. 2002 Apr;15(2):194–222.
  • Sly PD, Brennan S, Gangell C, de Klerk N, Murray C, Mott L, Stick SM, Robinson PJ, Robertson CF, Ranganathan SC. Lung disease at diagnosis in infants with cystic fibrosis detected by newborn screening. Am J Respir Crit Care Med. 2009 Jul 15;180(2):146–152.
  • Stick SM, Brennan S, Murray C, Douglas T, von Ungern-Sternberg BS, Garratt LW, Gangell CL, De Klerk N, Linnane B, Ranganathan S, Robinson P, Robertson C, Sly PD. Bronchiectasis in infants and preschool children diagnosed with cystic fibrosis after newborn screening. J Pediatr. 2009 Nov;155(5):623–628.e1.
  • Mott LS, Park J, Murray CP, Gangell CL, de Klerk NH, Robinson PJ, Robertson CF, Ranganathan SC, Sly PD, Stick SM. Progression of early structural lung disease in young children with cystic fibrosis assessed using CT. Thorax. 2012 Jun;67(6):509–516.
  • Connett GJ. Bronchoalveolar lavage. Paediatr Respir Rev. 2000 Mar;1(1):52–56.
  • Banerjee B, Kicic A, Musk M, Sutanto EN, Stick SM, Chambers DC. Successful establishment of primary small airway cell cultures in human lung transplantation. Respir Res. 2009 Jan;10:99–109.
  • Lane C, Burgess S, Kicic A, Knight D, Stick S. The use of non-bronchoscopic brushings to study the paediatric airway. Respir Res. 2005 Jan;6:53–63.
  • Kicic A, Sutanto EN, Stevens PT, Knight DA, Stick SM. Intrinsic biochemical and functional differences in bronchial epithelial cells of children with asthma. Am J Respir Crit Care Med. 2006 Nov 15;174(10):1110–1118.
  • Doherty GM, Christie SN, Skibinski G, Puddicombe SM, Warke TJ, de Courcey F, Cross AL, Lyons JDM, Ennis M, Shields MD, Heaney LG. Non-bronchoscopic sampling and culture of bronchial epithelial cells in children. Clin Exp Allergy. 2003 Sep;33(9):1221–1225.
  • Sutanto EN, Kicic A, Foo CJ, Stevens PT, Mullane D, Knight DA, Stick SM. Innate inflammatory responses of pediatric cystic fibrosis airway epithelial cells: effects of nonviral and viral stimulation. Am J Respir Cell Mol Biol. 2011;44(6):761–767.
  • Looi K, Sutanto EN, Banerjee B, Garratt L, Ling K-M, Foo CJ, Stick SM, Kicic A. Bronchial brushings for investigating airway inflammation and remodelling. Respirology. 2011 Jul;16(5):725–737.
  • Mosler K, Coraux C, Fragaki K, Zahm J-M, Bajolet O, Bessaci-Kabouya K, Puchelle E, Abély M, Mauran P. Feasibility of nasal epithelial brushing for the study of airway epithelial functions in CF infants. J Cyst Fibros. 2008 Jan;7(1):44–53.
  • Lopez-Souza N, Favoreto S, Wong H, Ward T, Yagi S, Schnurr D, Finkbeiner WE, Dolganov GM, Widdicombe JH, Boushey HA, Avila PC. In vitro susceptibility to rhinovirus infection is greater for bronchial than for nasal airway epithelial cells in human subjects. J Allergy Clin Immunol. 2009 Jun;123(6):1384–1390.e2.
  • Ogilvie V, Passmore M, Hyndman L, Jones L, Stevenson B, Wilson A, Davidson H, Kitchen RR, Gray RD, Shah P, Alton EW, Davies JC, Porteous DJ, Boyd AC. Differential global gene expression in cystic fibrosis nasal and bronchial epithelium. Genomics. 2011 Nov;98(5):327–336.
  • Kieninger E, Vareille M, Kopf BS, Blank F, Alves MP, Gisler FM, Latzin P, Casaulta C, Geiser T, Johnston SL, Edwards MR, Regamey N. Lack of an exaggerated inflammatory response on virus infection in cystic fibrosis. Eur Respir J. 2012 Feb;39(2):297–304.
  • De Blic J, Midulla F, Barbato A, Clement A, Dab I, Eber E, Green C, Grigg J, Kotecha S, Kurland G, Pohunek P, Ratjen F, Rossi G. Bronchoalveolar lavage in children. ERS Task Force on bronchoalveolar lavage in children. Eur Respir J. 2000 Jan;15(1):217–231.
  • McNamara PS, Kicic A, Sutanto EN, Stevens PT, Stick SM. Comparison of techniques for obtaining lower airway epithelial cells from children. Eur Respir J. 2008 Sep;32(3):763–768.
  • Strober W. Trypan blue exclusion test of cell viability. Curr Protoc Immunol. 2001 May; 21(3B):A.3B.1–A.3B.2.
  • Brennan S, Hall GL, Horak F, Moeller A, Pitrez PMC, Franzmann A, Turner S, de Klerk N, Franklin P, Winfield KR, Balding E, Stick SM, Sly PD. Correlation of forced oscillation technique in preschool children with cystic fibrosis with pulmonary inflammation. Thorax. 2005 Feb;60(2):159–163.
  • Franklin PJ, Hall GL, Moeller A, Horak F, Brennan S, Stick SM. Exhaled nitric oxide is not reduced in infants with cystic fibrosis. Eur Respir J. 2006 Feb;27(2):350–353.
  • Moeller A, Horak F, Lane C, Knight D, Kicic A, Brennan S, Franklin P, Terpolilli J, Wildhaber JH, Stick SM. Inducible NO synthase expression is low in airway epithelium from young children with cystic fibrosis. Thorax. 2006 Jun;61(6):514– 520.
  • Berry LJ, Sheil B, Garratt L, Sly PD. Stability of interleukin 8 and neutrophil elastase in bronchoalveolar lavage fluid following long-term storage. J Cyst Fibros. 2010 Sep;9(5):346–350.
  • Delacourt C, Hérigault S, Delclaux C, Poncin A, Levame M, Harf A, Saudubray F, Lafuma C Protection against acute lung injury by intravenous or intratracheal pretreatment with EPI-HNE-4, a new potent neutrophil elastase inhibitor. Am J Respir Cell Mol Biol. 2002 Mar;26(3):290–297.
  • Rowntree RK, Harris A. The phenotypic consequences of CFTR mutations. Ann Hum Genet. 2003 Sep;67(Pt 5):471–485.
  • Zabner J, Karp P, Seiler M, Phillips SL, Mitchell CJ, Saavedra M, Welsh M, Klingelhutz AJ. Development of cystic fibrosis and noncystic fibrosis airway cell lines. Am J Physiol Lung Cell Mol Physiol. 2003 May;284(5):L844–L854.
  • Campbell AM, Chanez P, Vignola AM, Bousquet J, Couret I, Michel FB, Godard P. Functional characteristics of bronchial epithelium obtained by brushing from asthmatic and normal subjects. Am Rev Respir Dis. 1993 Mar 1;147(3):529– 534.
  • Rieger AM, Nelson KL, Konowalchuk JD, Barreda DR. Modified annexin V/propidium iodide apoptosis assay for accurate assessment of cell death. J Vis Exp. 2011 Jan;(50):37–40.
  • McDougall CM, Blaylock MG, Douglas JG, Brooker RJ, Helms PJ, Walsh GM. Nasal epithelial cells as surrogates for bronchial epithelial cells in airway inflammation studies. Am J Respir Cell Mol Biol. 2008 Nov;39(5):560–568.
  • Knowles M, Gatzy J, Boucher R. Increased bioelectric potential difference across respiratory epithelia in cystic fibrosis. N Engl J Med. 1981 Dec 17;305(25):1489–1495.
  • Mogayzel PJ, Flume PA. Update in cystic fibrosis 2009. Am J Respir Crit Care Med. 2010 Mar 15;181(6):539–544.
  • Teichgräber V, Ulrich M, Endlich N, Riethmüller J, Wilker B, De Oliveira-Munding CC, van Heeckeren AM, Barr ML, von Kürthy G, Schmid KW, Weller M, Tümmler B, Lang F, Grassme H, Döring G, Gulbins E. Ceramide accumulation mediates inflammation, cell death and infection susceptibility in cystic fibrosis. Nat Med. 2008 Apr;14(4):382–391.
  • Guilbault C, De Sanctis JB, Wojewodka G, Saeed Z, Lachance C, Skinner TAA, Vilela RM, Kubow S, Lands LC, Hajduch M, Matouk E, Radzioch D. Fenretinide corrects newly found ceramide deficiency in cystic fibrosis. Am J Respir Cell Mol Biol. 2008 Jan 1;38(1):47–56.
  • Haggie PM, Verkman AS. Defective organellar acidification as a cause of cystic fibrosis lung disease: reexamination of a recurring hypothesis. Am J Physiol Lung Cell Mol Physiol. 2009 Jun;296(6):L859–L867.
  • Painter RG, Valentine VG, Lanson NA, Leidal K, Zhang Q, Lombard G, Thompson C, Viswanathan A, Nauseef WM, Wang G, Wang G. CFTR Expression in human neutrophils and the phagolysosomal chlorination defect in cystic fibrosis. Biochemistry. 2006 Aug 29;45(34):10260–10269.
  • Bruscia EM, Zhang P-X, Satoh A, Caputo C, Medzhitov R, Shenoy A, Egan ME, Krause DS. Abnormal trafficking and degradation of TLR4 underlie the elevated inflammatory response in cystic fibrosis. J Immunol. 2011 Jun 15;186(12):6990–6998.
  • Di A, Brown ME, Deriy L V, Li C, Szeto FL, Chen Y, Huang P, Tong J, Naren AP, Bindokas V, Palfrey HC, Nelson DJ. CFTR regulates phagosome acidification in macrophages and alters bactericidal activity. Nat Cell Biol. 2006 Sep;8(9):933–944.
  • Ginzberg HH, Shannon PT, Suzuki T, Hong O, Vachon E, Moraes T, Abreu MTH, Cherepanov V, Wang X, Chow C-W, Downey GP. Leukocyte elastase induces epithelial apoptosis: role of mitochondial permeability changes and Akt. Am J Physiol Gastrointest Liver Physiol. 2004 Jul;287(1):G286–G298.
  • Suzuki T, Yamashita C, Zemans RL, Briones N, Van Linden A, Downey GP. Leukocyte elastase induces lung epithelial apoptosis via a PAR-1-, NF-kappaB-, and p53-dependent pathway. Am J Respir Cell Mol Biol. 2009 Dec;41(6):742–755.
  • Fischer BM, Wong JK, Degan S, Kummarapurugu AB, Zheng S, Haridass P, Voynow JA. Increased expression of senescence markers in cystic fibrosis airways. Am J Physiol Lung Cell Mol Physiol. 2013 Mar 15;304(6):L394–L400.
  • Standiford TJ, Kunkel SL, Basha MA, Chensue SW, Lynch JP, Toews GB, Westwick J, Strieter RM. Interleukin-8 gene expression by a pulmonary epithelial cell line. A model for cytokine networks in the lung. J Clin Invest. 1990 Dec 1;86(6):1945–1953.
  • Kunkel SL, Standiford T, Kasahara K, Strieter RM. Interleukin-8 (IL-8): the major neutrophil chemotactic factor in the lung. Exp Lung Res. 1991;17(1):17–23.
  • Zabner J, Scheetz TE, Almabrazi HG, Casavant TL, Huang J, Keshavjee S, McCray PB. CFTR DeltaF508 mutation has minimal effect on the gene expression profile of differentiated human airway epithelia. Am J Physiol Lung Cell Mol Physiol. 2005 Oct;289(4):L545–L553.
  • Mercer RR, Russell ML, Roggli VL, Crapo JD. Cell number and distribution in human and rat airways. Am J Respir Cell Mol Biol. 1994 Jun;10(6):613–624.
  • Boucher RC. Regulation of airway surface liquid volume by human airway epithelia. Pflugers Arch. 2003 Jan;445(4):495–498.
  • Brennan S. Innate immune activation and cystic fibrosis. Paediatr Respir Rev. 2008 Dec;9(4):271–279.
  • Crosby LM, Waters CM. Epithelial repair mechanisms in the lung. Am J Physiol Lung Cell Mol Physiol. 2010 Jun 1;298(6):L715–L731.
  • Piorunek T, Marszalek A, Biczysko W, Gozdzik J, Cofta S, Seget M. Correlation between the stage of cystic fibrosis and the level of morphological changes in adult patients. J Physiol Pharmacol. 2008 Dec;59(Suppl. 6):565–572.
  • Machen TE. Innate immune response in CF airway epithelia: hyperinflammatory? Am J Physiol Cell Physiol. 2006 Aug;291(2):C218–C230.
  • Loveday RL, Speirs V, Drew PJ, Kerin MJ, Monson JRT, Greenman J. Intracellular flow cytometric analysis of primary cultured breast tumor cells. Cancer Invest. 2002 Jan;20(3):340–347.

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