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Intrauterine growth restriction predisposes to airway inflammation without disruption of epithelial integrity in postnatal male mice

Published online by Cambridge University Press:  17 August 2020

Kevin Looi
Affiliation:
Telethon Kids Institute, The University of Western Australia, Crawley, WA6009, Australia School of Public Health, Curtin University, Bentley, WA6102, Australia
Anthony Kicic
Affiliation:
Telethon Kids Institute, The University of Western Australia, Crawley, WA6009, Australia School of Public Health, Curtin University, Bentley, WA6102, Australia Faculty of Health and Medical Science, The University of Western Australia, Crawley, WA6009, Australia Department of Respiratory and Sleep Medicine, Perth Children’s Hospital, Nedlands, WA6009, Australia Centre for Cell Therapy and Regenerative Medicine, The University of Western Australia, Crawley, WA6009, Australia
Peter B. Noble
Affiliation:
School of Human Sciences, The University of Western Australia, Crawley, WA6009, Australia
Kimberley C. W. Wang*
Affiliation:
Telethon Kids Institute, The University of Western Australia, Crawley, WA6009, Australia School of Human Sciences, The University of Western Australia, Crawley, WA6009, Australia
*
Address for correspondence: Dr Kimberley Wang, School of Human Sciences, The University of Western Australia, 35 Stirling Highway, Crawley, WA6009, Australia. Email: kimberley.wang@uwa.edu.au

Abstract

Evidence from animal models demonstrate that intrauterine growth restriction (IUGR) alters airway structure and function which may affect susceptibility to disease. Airway inflammation and dysregulated epithelial barrier properties are features of asthma which have not been examined in the context of IUGR. This study used a maternal hypoxia-induced IUGR mouse model to assess lung-specific and systemic inflammation and airway epithelial tight junctions (TJs) protein expression. Pregnant BALB/c mice were housed under hypoxic conditions (10.5% O2) from gestational day (GD) 11 to 17.5 (IUGR group; term, GD 21). Following hypoxic exposure, mice were returned to a normoxic environment (21% O2). A Control group was housed under normoxic conditions throughout pregnancy. Offspring weights were recorded at 2 and 8 weeks of age and euthanized for bronchoalveolar lavage (BAL) and peritoneal cavity fluid collection for inflammatory cells counts. From a separate group of mice, right lungs were collected for Western blotting of TJs proteins. IUGR offspring had greater inflammatory cells in the BAL fluid but not in peritoneal fluid compared with Controls. At 8 weeks of age, interleukin (IL)-2, IL-13, and eotaxin concentrations were higher in male IUGR compared with male Control offspring but not in females. IUGR had no effect on TJs protein expression. Maternal hypoxia-induced IUGR increases inflammatory cells in the BAL fluid of IUGR offspring with no difference in TJs protein expression. Increased cytokine release, specific to the lungs of IUGR male offspring, indicates that both IUGR and sex can influence susceptibility to airway disease.

Type
Original Article
Copyright
© Cambridge University Press and the International Society for Developmental Origins of Health and Disease 2020

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References

AIHW. Australia’s Mothers and Babies 2015—In Brief. 2015; p. 12. Canberra: AIHW.Google Scholar
Källén, B, Finnström, O, Nygren, KG, Otterblad Olausson, P. Association between preterm birth and intrauterine growth retardation and child asthma. Eur Respir J. 2013; 41(3), 671676.10.1183/09031936.00041912CrossRefGoogle ScholarPubMed
Villamor, E, Iliadou, A, Cnattingius, S. Is the association between low birth weight and asthma independent of genetic and shared environmental factors? Am J Epidemiol. 2009; 169(11), 13371343.CrossRefGoogle ScholarPubMed
Wang, KCW, Larcombe, AN, Berry, LJ, et al. Foetal growth restriction in mice modifies postnatal airway responsiveness in an age and sex-dependent manner. Clin Sci (Lond). 2018; 132(2), 273284.CrossRefGoogle Scholar
Wang, KCW, Morton, JS, Davidge, ST, et al. Increased heterogeneity of airway calibre in adult rats after hypoxia-induced intrauterine growth restriction. Respirology. 2017; 22(7), 13291335.CrossRefGoogle ScholarPubMed
Noble, PB, Kowlessur, D, Larcombe, AN, Donovan, GM, Wang, KCW. Mechanical abnormalities of the airway wall in adult mice after intrauterine growth restriction. Front Physiol. 2019; 10, 1073.CrossRefGoogle ScholarPubMed
Wang, KCW, Noble, PB. Foetal growth restriction and asthma: Airway smooth muscle thickness rather than just lung size? Respirology. 2020; 25(8), 889891. doi: 10.1111/resp.13851 CrossRefGoogle ScholarPubMed
Farquhar, MG, Palade, GE. Junctional complexes in various epithelia. J Cell Biol. 1963; 17, 375412.10.1083/jcb.17.2.375CrossRefGoogle ScholarPubMed
Hammad, H, Chieppa, M, Perros, F, Willart, MA, Germain, RN, Lambrecht, BN. House dust mite allergen induces asthma via Toll-like receptor 4 triggering of airway structural cells. Nat Med. 2009; 15(4), 410.CrossRefGoogle ScholarPubMed
Nathan, AT, Peterson, EA, Chakir, J, Wills-Karp, M. Innate immune responses of airway epithelium to house dust mite are mediated through β-glucan–dependent pathways. J Allergy Clin Immunol. 2009; 123(3), 612618.10.1016/j.jaci.2008.12.006CrossRefGoogle ScholarPubMed
Sajjan, U. Rhinovirus disrupts the barrier function of polarized airway epithelial cells. Am J Respir Crit Care Med. 2008; 178(12), 1271.CrossRefGoogle ScholarPubMed
Van Winkle, LS, Gunderson, AD, Shimizu, JA, Baker, GL, Brown, CD. Gender differences in naphthalene metabolism and naphthalene-induced acute lung injury. Am J Physiol Lung Cell Mol Physiol. 2002; 282(5), L1122L1134.CrossRefGoogle ScholarPubMed
Degano, B, Prevost, MC, Berger, P, et al. Estradiol decreases the acetylcholine-elicited airway reactivity in ovariectomized rats through an increase in epithelial acetylcholinesterase activity. Am J Respir Crit Care Med. 2001; 164(10 Pt 1), 18491854.CrossRefGoogle ScholarPubMed
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; 174(10), 11101118.CrossRefGoogle ScholarPubMed
Looi, K, Buckley, A, Rigby, P, et al. Effects of human rhinovirus on epithelial barrier integrity and function in children with asthma. Clin Exp Allergy. 2018; 48(5), 513524.CrossRefGoogle ScholarPubMed
Wilcox, CR, Jones, CE. Beyond passive immunity: is there priming of the fetal immune system following vaccination in pregnancy and what are the potential clinical implications? Front Immunol. 2018; 9, 1548.CrossRefGoogle ScholarPubMed
Wooldridge, AL, Bischof, RJ, Meeusen, EN, et al. Placental restriction of fetal growth reduces cutaneous responses to antigen after sensitization in sheep. Am J Physiol Regul Integr Comp Physiol. 2014; 306(7), R441R446.CrossRefGoogle Scholar
Francis, MR, Pinniger, GJ, Noble, PB, Wang, KCW. Intrauterine growth restriction affects diaphragm function in adult female and male mice. Pediatr Pulmonol. 2020; 55(1), 229235.CrossRefGoogle ScholarPubMed
Wiest, R, Leidl, F, Kopp, A, et al. Peritoneal fluid adipokines: ready for prime time? Eur J Clin Invest. 2009; 39(3), 219229.CrossRefGoogle ScholarPubMed
Glitz, C, Souza, C, Rodini, GP, et al. Peritoneal and serum interleukin-18 levels are not increased in women with minimum or mild endometriosis. Braz J Med Biol Res. 2009; 42(11), 10391043.CrossRefGoogle ScholarPubMed
Ray, A, Dittel, BN. Isolation of mouse peritoneal cavity cells. J Vis Exp. 2010(35), e1488.Google Scholar
Larcombe, AN, Janka, MA, Mullins, BJ, Berry, LJ, Bredin, A, Franklin, PJ. The effects of electronic cigarette aerosol exposure on inflammation and lung function in mice. Am J Physiol Lung Cell Mol Physiol. 2017; 313(1), L67L79.CrossRefGoogle ScholarPubMed
Holgate, ST. The sentinel role of the airway epithelium in asthma pathogenesis. Immunol Rev. 2011; 242(1), 205219.CrossRefGoogle ScholarPubMed
Sonnenschein-van der Voort, AM, Gaillard, R, de Jongste, JC, Hofman, A, Jaddoe, VW, Duijts, L. Foetal and infant growth patterns, airway resistance and school-age asthma. Respirology. 2016; 21(4), 674682.10.1111/resp.12718CrossRefGoogle ScholarPubMed
Myers, TR. Pediatric asthma epidemiology: incidence, morbidity, and mortality. Respir Care Clin N Am. 2000; 6(1), 114.CrossRefGoogle ScholarPubMed
Schatz, M, Camargo, CA Jr . The relationship of sex to asthma prevalence, health care utilization, and medications in a large managed care organization. Ann Allergy Asthma Immunol. 2003; 91(6), 553558.CrossRefGoogle Scholar
Wignarajah, D, Cock, ML, Pinkerton, KE, Harding, R. Influence of intrauterine growth restriction on airway development in fetal and postnatal sheep. Pediatr Res. 2002; 51(6), 681.10.1203/00006450-200206000-00004CrossRefGoogle ScholarPubMed
Soo, JY, Orgeig, S, McGillick, EV, Zhang, S, McMillen, IC, Morrison, JL. Normalisation of surfactant protein-A and -B expression in the lungs of low birth weight lambs by 21 days old. PLoS One. 2017; 12(9), e0181185.CrossRefGoogle Scholar
Lipsett, J, Tamblyn, M, Madigan, K, et al. Restricted fetal growth and lung development: a morphometric analysis of pulmonary structure. Pediatr Pulmonol. 2006; 41(12), 11381145.CrossRefGoogle ScholarPubMed
Hargreave, FE, Dolovich, J, O’Byrne, PM, Ramsdale, EH, Daniel, EE. The origin of airway hyperresponsiveness. J Allergy Clin Immunol. 1986; 78(5), 825832.CrossRefGoogle ScholarPubMed
Cockcroft, DW, Davis, BE. Mechanisms of airway hyperresponsiveness. J Allergy Clin Immunol. 2006; 118(3), 551559.CrossRefGoogle ScholarPubMed
O’Byrne, PM, Inman, MD. Airway hyperresponsiveness. Chest. 2003; 123(3), 411S416S.CrossRefGoogle ScholarPubMed
Fahy, JV, Corry, DB, Boushey, HA. Airway inflammation and remodeling in asthma. Curr Opin Pulm Med. 2000; 6(1), 1520.CrossRefGoogle ScholarPubMed
Ling, KM, Sutanto, EN, Iosifidis, T, et al. Reduced transforming growth factor β1 (TGF-β1) in the repair of airway epithelial cells of children with asthma. Respirology. 2016; 21(7), 12191226.10.1111/resp.12810CrossRefGoogle ScholarPubMed
Lambrecht, BN, Hammad, H. The airway epithelium in asthma. Nat Med. 2012; 18(5), 684692.CrossRefGoogle ScholarPubMed
Fahy, JV, Locksley, RM. The airway epithelium as a regulator of Th2 responses in asthma. Am J Respir Crit Care Med. 2011; 184(4), 390392.CrossRefGoogle ScholarPubMed
Coyne, C, Vanhook, M, Gambling, T, Carson, J, Boucher, R, Johnson, L. Regulation of airway tight junctions by proinflammatory cytokines. Mol Biol Cell. 2002; 13(9), 32183234.10.1091/mbc.e02-03-0134CrossRefGoogle ScholarPubMed
Morrison, KJ, Gao, Y, Vanhoutte, PM. Epithelial modulation of airway smooth muscle. Am J Physiol Lung Cell Mol Physiol. 1990; 258(6), L254L262.CrossRefGoogle ScholarPubMed
Xia, YC, Harris, T, Stewart, AG, Mackay, GA. Secreted factors from human mast cells trigger inflammatory cytokine production by human airway smooth muscle cells. Int Arch Allergy Immunol. 2013; 160(1), 7585.CrossRefGoogle ScholarPubMed
Rackley, CR, Stripp, BR. Building and maintaining the epithelium of the lung. J Clin Invest. 2012; 122(8), 27242730.10.1172/JCI60519CrossRefGoogle ScholarPubMed
Costabel, U, Guzman, J. Bronchoalveolar lavage in interstitial lung disease. Curr Opin Pulm Med. 2001; 7(5), 255261.CrossRefGoogle ScholarPubMed
Wittekindt, OH. Tight junctions in pulmonary epithelia during lung inflammation. Pflugers Arch. 2017; 469(1), 135147.CrossRefGoogle ScholarPubMed
Pascoe, CD. Unravelling the impact of early life exposures on lung structure and function in the developmental origins of asthma. Respirology. 2017; 22(7), 12411242.10.1111/resp.13098CrossRefGoogle ScholarPubMed
Raghupathy, R, Al-Azemi, M, Azizieh, F. Intrauterine growth restriction: cytokine profiles of trophoblast antigen-stimulated maternal lymphocytes. Clin Dev Immunol. 2011; 2012.Google ScholarPubMed
Chakraborty, S, Islam, S, Saha, S, Ain, R. Dexamethasone-induced Intra-Uterine Growth Restriction impacts NOSTRIN and its downstream effector genes in the rat mesometrial uterus. Sci Rep. 2018; 8(1), 8342.CrossRefGoogle ScholarPubMed
Wixey, JA, Lee, KM, Miller, SM, et al. Neuropathology in intrauterine growth restricted newborn piglets is associated with glial activation and proinflammatory status in the brain. J Neuroinflammation. 2019; 16(1), 5.CrossRefGoogle Scholar
Alcazar, MAA, Östreicher, I, Appel, S, et al. Developmental regulation of inflammatory cytokine-mediated Stat3 signaling: the missing link between intrauterine growth restriction and pulmonary dysfunction? J Mol Med (Berl). 2012; 90(8), 945957.CrossRefGoogle Scholar
Whyte, MK, Walmsley, SR. The regulation of pulmonary inflammation by the hypoxia-inducible factor–hydroxylase oxygen-sensing pathway. Ann Am Thorac Soc. 2014; 11(Supplement 5), S271S276.CrossRefGoogle ScholarPubMed
Eltzschig, HK, Carmeliet, P. Hypoxia and inflammation. N Engl J Med. 2011; 364(7), 656665.CrossRefGoogle ScholarPubMed
Rueda-Clausen, CF, Morton, JS, Davidge, ST. Effects of hypoxia-induced intrauterine growth restriction on cardiopulmonary structure and function during adulthood. Cardiovasc Res. 2008; 81(4), 713722.10.1093/cvr/cvn341CrossRefGoogle ScholarPubMed
Baek, KJ, Cho, JY, Rosenthal, P, Alexander, LEC, Nizet, V, Broide, DH. Hypoxia potentiates allergen induction of HIF-1α, chemokines, airway inflammation, TGF-β1, and airway remodeling in a mouse model. Clin Immunol. 2013; 147(1), 2737.10.1016/j.clim.2013.02.004CrossRefGoogle ScholarPubMed
Matsukura, S, Stellato, C, Georas, SN, et al. Interleukin-13 upregulates eotaxin expression in airway epithelial cells by a STAT6-dependent mechanism. Am J Respir Cell Mol Biol. 2001; 24(6), 755761.CrossRefGoogle ScholarPubMed
Wills-Karp, M, Luyimbazi, J, Xu, X, et al. Interleukin-13: central mediator of allergic asthma. Science. 1998; 282(5397), 22582261.CrossRefGoogle ScholarPubMed
Grünig, G, Warnock, M, Wakil, AE, et al. Requirement for IL-13 independently of IL-4 in experimental asthma. Science. 1998; 282(5397), 22612263.CrossRefGoogle ScholarPubMed
Nag, S, Lamkhioued, B, Renzi, PM. Interleukin-2–induced increased airway responsiveness and lung Th2 cytokine expression occur after antigen challenge through the leukotriene pathway. Am J Respir Crit Care Med. 2002; 165(11), 15401545.CrossRefGoogle ScholarPubMed
Chiba, Y, Nakazawa, S, Todoroki, M, Shinozaki, K, Sakai, H, Misawa, M. Interleukin-13 augments bronchial smooth muscle contractility with an up-regulation of RhoA protein. Am J Respir Cell Mol Biol. 2009; 40(2), 159167.10.1165/rcmb.2008-0162OCCrossRefGoogle ScholarPubMed
Almqvist, C, Worm, M, Leynaert, B, ‘Gender’ ftwgoGLW. Impact of gender on asthma in childhood and adolescence: a GA2LEN review. Allergy. 2008; 63(1), 4757.Google ScholarPubMed
Uekert, SJ, Akan, G, Evans, MD, et al. Sex-related differences in immune development and the expression of atopy in early childhood. J Allergy Clin Immunol. 2006; 118(6), 13751381.CrossRefGoogle ScholarPubMed
Riffo-Vasquez, Y, Ligeiro de Oliveira, A, Page, C, Spina, D, Tavares-de-Lima W. Role of sex hormones in allergic inflammation in mice. Clin Exp Allergy. 2007; 37(3), 459470.10.1111/j.1365-2222.2007.02670.xCrossRefGoogle ScholarPubMed
Antunes, MA, Abreu, SC, Silva, AL, et al. Sex-specific lung remodeling and inflammation changes in experimental allergic asthma. J Appl Physiol. 2010; 109(3), 855863.CrossRefGoogle ScholarPubMed
Becerra-Díaz, M, Strickland, AB, Keselman, A, Heller, NM. Androgen and androgen receptor as enhancers of M2 macrophage polarization in allergic lung inflammation. J Immunol. 2018; 201(10), 29232933.CrossRefGoogle ScholarPubMed
Barrat, F, Lesourd, B, Boulouis, HJ, et al. Sex and parity modulate cytokine production during murine ageing. Clin Exp Immunol. 1997; 109(3), 562568.CrossRefGoogle ScholarPubMed
Matha, L, Shim, H, Steer, CA, Yin, YH, Martinez-Gonzalez, I, Takei, F. Female and male mouse lung group 2 innate lymphoid cells differ in gene expression profiles and cytokine production. PLoS One. 2019; 14(3), e0214286.CrossRefGoogle ScholarPubMed
Barnes, PJ. Targeting cytokines to treat asthma and chronic obstructive pulmonary disease. Nat Rev Immunol. 2018; 18(7), 454466.CrossRefGoogle ScholarPubMed
Noble, PB, Turner, DJ, Mitchell, HW. Relationship of airway narrowing, compliance, and cartilage in isolated bronchial segments. J Appl Physiol. 2002; 92(3), 11191124.CrossRefGoogle ScholarPubMed
Cairncross, A, Noble, PB, McFawn, PK. Hyperinflation of bronchi in vitro impairs bronchodilation to simulated breathing and increases sensitivity to contractile activation. Respirology. 2018; 23(8), 750755.CrossRefGoogle ScholarPubMed
Noble, PB, McFawn, PK, Mitchell, HW. Responsiveness of the isolated airway during simulated deep inspirations: Effect of airway smooth muscle stiffness and strain. J Appl Physiol (1985). 2007; 103(3), 787795.CrossRefGoogle ScholarPubMed
Anderson, JM, Van Itallie, CM. Physiology and function of the tight junction. Cold Spring Harb Perspect Biol. 2009; 1(2), a002584.CrossRefGoogle ScholarPubMed
Berthiaume, Y, Matthay, MA. Alveolar edema fluid clearance and acute lung injury. Respir Physiol Neurobiol. 2007; 159(3), 350359.CrossRefGoogle ScholarPubMed
LaFemina, MJ, Sutherland, KM, Bentley, T, et al. Claudin-18 deficiency results in alveolar barrier dysfunction and impaired alveologenesis in mice. Am J Respir Cell Mol Biol. 2014; 51(4), 550558.CrossRefGoogle ScholarPubMed
Georas, SN, Rezaee, F. Epithelial barrier function: at the front line of asthma immunology and allergic airway inflammation. J Allergy Clin Immunol. 2014; 134(3), 509520.CrossRefGoogle ScholarPubMed
Olson, N, Hristova, M, Heintz, NH, Lounsbury, KM, Van Der Vliet, A. Activation of hypoxia-inducible factor-1 protects airway epithelium against oxidant-induced barrier dysfunction. Am J Physiol Lung Cell Mol Physiol. 2011; 301(6), L993L1002.CrossRefGoogle ScholarPubMed