Age-dependent changes in porcine alveolar macrophage function during the postnatal period of alveolarization

Developmental and Comparative Immunology

Volumn 33, Issue 2, 2009, Pages 145-151

  Dickie, R ^a   Tasat, D R ^b   Alanis, E Fernandez ^b   Delfosse, V ^b   Tsuda, A ^a  

^a HARVARD SCHOOL OF PUBLIC HEALTH   (United States)

^b UNIVERSIDAD NACIONAL DE SAN MARTÍN   (Argentina)

Author keywords

Bronchoalveolar lavage; Lung; Neonate; Ontogeny; Phagocytosis; Pig; ROS; Superoxide anion

Indexed keywords

REACTIVE OXYGEN METABOLITE;

AEROBIC METABOLISM; AGE; ALVEOLARIZATION; ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; CONTROLLED STUDY; LUNG ALVEOLUS; LUNG ALVEOLUS MACROPHAGE; LUNG DEVELOPMENT; LUNG LAVAGE; MALE; NONHUMAN; PHAGOCYTOSIS; POSTNATAL DEVELOPMENT; PRIORITY JOURNAL; SWINE;

MAMMALIA; SUIDAE; SUS;

EID: 54849425530     PISSN: 0145305X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.dci.2008.07.016     Document Type: Article

References (42)

1. Finkelstein J.N., and Johnston C.J. Enhanced sensitivity of the postnatal lung to environmental insults and oxidant stress. Pediatrics 113 4 Suppl (2004) 1092-1096
2. Yeo S.P., Stokes C.R., Taylor F.G., and Bourne F.J. Maturation of cellular defence in the respiratory tract of young calves. Res Vet Sci 55 3 (1993) 292-297
3. Weiss R.A., Chanana A.D., and Joel D.D. Postnatal maturation of pulmonary antimicrobial defense mechanisms in conventional and germ-free lambs. Pediatr Res 20 6 (1986) 496-504
4. Zink M.C., and Johnson J.A. Cellular constituents of clinically normal foal bronchoalveolar lavage fluid during postnatal maturation. Am J Vet Res 45 5 (1984) 893-897
5. Bakker J.M., Broug-Holub E., Kroes H., van Rees E.P., Kraal G., and van Iwaarden J.F. Functional immaturity of rat alveolar macrophages during postnatal development. Immunology 94 3 (1998) 304-309
6. Jackson J.C., Palmer S., Wilson C.B., Standaert T.A., Truog W.E., Murphy J.H., et al. Postnatal changes in lung phospholipids and alveolar macrophages in term newborn monkeys. Respir Physiol 73 3 (1988) 289-300
7. Goldman A., Rubin C., Gomez S., Palermo M.S., and Tasat D.R. Functional age-dependent changes in bronchoalveolar lavage rat cells. Cell Mol Biol (Noisy-le-grand) 50 (2004) OL649-655 (Online Pub)
8. Zeidler R.B., and Kim H.D. Phagocytosis, chemiluminescence, and cell volume of alveolar macrophages from neonatal and adult pigs. J Leukoc Biol 37 1 (1985) 29-43
9. Tasat D.R., Mancuso R., O'Connor S., and Molinari B. Age-dependent change in reactive oxygen species and nitric oxide generation by rat alveolar macrophages. Aging Cell 2 3 (2003) 159-164
10. Kojima T., Hattori K., Fujiwara T., Hirata Y., and Kobayashi Y. Maturational changes in superoxide anion production of rabbit alveolar macrophages. Life Sci 55 12 (1994) 911-915
11. Bellanti J.A., and Zeligs B.J. Developmental aspects of pulmonary defenses in children. Pediatr Pulmonol Suppl 11 (1995) 79-80
12. Coonrod J.D., Jarrells M.C., and Bridges R.B. Impaired pulmonary clearance of pneumococci in neonatal rats. Pediatr Res 22 6 (1987) 736-742
13. Kurland G., Cheung A.T., Miller M.E., Ayin S.A., Cho M.M., and Ford E.W. The ontogeny of pulmonary defenses: alveolar macrophage function in neonatal and juvenile rhesus monkeys. Pediatr Res 23 3 (1988) 293-297
14. Weiss R.A., Chanana A.D., and Joel D.D. The status of pulmonary host defense in the neonatal sheep: cellular and humoral aspects. Ann NY Acad Sci 459 (1985) 40-55
15. Taylor P.R., Martinez-Pomares L., Stacey M., Lin H.H., Brown G.D., and Gordon S. Macrophage receptors and immune recognition. Annu Rev Immunol 23 (2005) 901-944
16. Babior B.M. Phagocytes and oxidative stress. Am J Med 109 1 (2000) 33-44
17. Fernandez M.L., Duran H.A., O'Connor S.E., Cabrini R.L., and Molinari B.L. Role of distinct subpopulations of peritoneal macrophages in the regulation of reactive oxygen species release. Free Radic Biol Med 27 7/8 (1999) 797-809
18. Delacourt C., d'Ortho M.P., Macquin-Mavier I., Pezet S., Housset B., Lafuma C., et al. Oxidant-antioxidant balance in alveolar macrophages from newborn rats. Eur Respir J 9 12 (1996) 2517-2524
19. Zeltner T.B., and Burri P.H. The postnatal development and growth of the human lung, II. Morphology. Respir Physiol 67 3 (1987) 269-282
20. Grigg J., and Riedler J. Developmental airway cell biology The "normal" young child. Am J Respir Crit Care Med 162 2 Pt 2 (2000) S52-55
21. Kato M., Tokuyama K., Minakami H., Nagai A., Kozawa K., Goto H., et al. Increased superoxide radicals generation from alveolar macrophages in immature guinea-pigs. Cell Biol Int 26 9 (2002) 829-832
22. Mansell A.L., Collins M.H., Johnson Jr. E., and Gil J. Postnatal growth of lung parenchyma in the piglet: morphometry correlated with mechanics. Anat Rec 241 1 (1995) 99-104
23. Winkler G.C., and Cheville N.F. The neonatal porcine lung: ultrastructural morphology and postnatal development of the terminal airways and alveolar region. Anat Rec 210 2 (1984) 303-313
24. Winkler G.C., and Cheville N.F. Morphometry of postnatal development in the porcine lung. Anat Rec 211 4 (1985) 427-433
25. Brain J., and Corkery G. The effect of increased particles on the endocytosis of radiocolloids by pulmonary macrophages in vivo: competitive and cytotoxic effects. In: Walton W. (Ed). Inhaled particles (1977), Pergamon, New York 551-564
26. Tasat D.R., and de Rey B.M. Cytotoxic effect of uranium dioxide on rat alveolar macrophages. Environ Res 44 1 (1987) 71-81
27. Segal A.W. Nitroblue-tetrazolium tests. Lancet 2 7891 (1974) 1248-1252
28. Mansell A.L., Moalli R.R., Calista C.L., and Pipkin A.C. Elastic moduli of lungs during postnatal development in the piglet. J Appl Physiol 67 4 (1989) 1422-1427
29. Greywoode G.I., McCarthy S.P., and McGee J.O. Labelling of cells of the mononuclear phagocyte system in routinely processed archival biopsy specimens with monoclonal antibody EBM/11. J Clin Pathol 43 12 (1990) 992-996
30. Ackermann M.R., DeBey B.M., Stabel T.J., Gold J.H., Register K.B., and Meehan J.T. Distribution of anti-CD68 (EBM11) immunoreactivity in formalin-fixed, paraffin-embedded bovine tissues. Vet Pathol 31 3 (1994) 340-348
31. Kudrin A., and Ray D. Cunning factor: macrophage migration inhibitory factor as a redox-regulated target. Immunol Cell Biol (2007)
32. Kevill K.A., Bhandari V., Kettunen M., Leng L., Fan J., Mizue Y., et al. A role for macrophage migration inhibitory factor in the neonatal respiratory distress syndrome. J Immunol 180 1 (2008) 601-608
33. Farver C.F., and Kobzik L. Lung macrophage differentiation antigens in developing fetal and newborn rat lungs: a quantitative flow cytometric analysis with immunohistochemistry. Lung 177 4 (1999) 205-217
34. Rau G.A., Vieten G., Haitsma J.J., Freihorst J., Poets C., Ure B.M., et al. Surfactant in newborn compared with adolescent pigs: adaptation to neonatal respiration. Am J Respir Cell Mol Biol 30 5 (2004) 694-701
35. Hardy B., Skutelsky E., Globerson A., and Danon D. Ultrastructural differences between macrophages of newborn and adult mice. J Reticuloendothel Soc 19 5 (1976) 291-299
36. Talbot R.J., Kellington J.P., and Morgan A. Are macrophages recovered from mouse lung by bronchoalveolar lavage representative of the alveolar macrophage pool?. Inhal Toxicol 8 (1996) 201-212
37. Edelman J., Cardozo C., and Lesser M. Lipopolysaccharide stimulates alveolar macrophage adherence in vivo and in vitro. Agents Actions 26 3/4 (1989) 287-291
38. Oliver M.H., Cole P.J., and Laurent G.J. Comparison of protein-synthesis rate of alveolar macrophages in vivo and in vitro. Biochem J 217 3 (1984) 761-765
39. Ellender M., Hodgson A., Wood K.L., and Moody J.C. Effect of bronchopulmonary lavage on lung retention and clearance of particulate material in hamsters. Environ Health Perspect 97 (1992) 209-213
40. Falini B., Flenghi L., Pileri S., Gambacorta M., Bigerna B., Durkop H., et al. PG-M1: a new monoclonal antibody directed against a fixative-resistant epitope on the macrophage-restricted form of the CD68 molecule. Am J Pathol 142 5 (1993) 1359-1372
41. Splichal I., Trebichavsky I., Splichalova A., Ditetova L., and Zahradnickova M. Escherichia coli administered into pig amniotic cavity appear in fetal airways and attract macrophages into fetal lungs. Physiol Res 51 5 (2002) 523-528
42. Perez-Reinado E., Ramirez-Boo M., Garrido J.J., Jorrin J.V., and Moreno A. Towards a global analysis of porcine alveolar macrophages proteins through two-dimensional electrophoresis and mass spectrometry. Dev Comp Immunol 31 12 (2007) 1220-1232