Congenital Alveolar Proteinosis in the Netherlands: A Report of Five Cases with Immunohistochemical and Genetic Studies on Surfactant Apoproteins

References

• Rosen H S, Castleman B, Liebow A A, Enzinger F M, Hunt R TN. Pulmonary alveolar proteinosis. N Engl J Med 1958; 258: 1123–42
   PubMed Web of Science ®Google Scholar
• Moulton S L, Krous H F, Merritt T A, et al. Congenital pulmonary alveolar proteinosis: Failure of treatment with extracorporeal life support. J Pediatr 1992; 120: 297–302
   PubMed Web of Science ®Google Scholar
• DeMello D E, Nogee L M, Heymans S, et al. Molecular and phenotypic variability in the congenital alveolar proteinosis syndrome associated with inherited surfactant protein B deficiency. J Pediatr 1994; 125: 43–50
   PubMed Web of Science ®Google Scholar
• Voorhout W F, Veenendaal T, Haagsman H P, Verkley A J, van Golde L MG, Geuze H J. Surfactant protein A is located at the corners of the pulmonary tubular myelin lattice. J Histochem Cytochem 1991; 39: 1331–6
   PubMed Web of Science ®Google Scholar
• Ogasawara Y, Kuroki Y, Shiratory M, Shimizu H, Miyamura K, Akino T. Ontogeny of surfactant apoprotein D, SP-D, in the rat lung. Biochim Biophys Acta 1991; 1083: 252–6
   PubMed Web of Science ®Google Scholar
• Voorhout W F, Veenendaal T, Kuroki Y, Osagawa Y, van Golde L MG, Geuze H J. Immunohistochemical localization of surfactant protein D (SP-D) in type II cells, Clara cells and alveolar macrophages of the rat lung. J Histochem Cytochem 1992; 40: 1589–97
   PubMed Web of Science ®Google Scholar
• Voorhout W F, Weaver T E, Haagsman H P, Geuze H J, van Golde L MG. Biosynthetic routing of pulmonary surfactant proteins in alveolar type II cells. Microsc Res Tech 1993; 26: 366–73
   PubMedGoogle Scholar
• Suzuki Y, Fujita Y, Kogishi K. Reconstruction of tubular myelin from synthetic lipids and proteins associated with pig pulmonary surfactant. Am Rev Respir Dis 1989; 140: 75–81
   PubMed Web of Science ®Google Scholar
• Sambrook J, Fritsch E F, Maniatis T. Molecular Cloning: A Laboratory Manual. Cold Spring Harbor Laboratory, Cold Spring Harbor, NY 1989; 9.17–9.19
   Google Scholar
• Pilot-Matias T J, Kister S E, Fox J L, Kropp K, Glasser S W, Whitsett J A. Structure and organization of the gene encoding human pulmonary surfactant proteolipid SP-B. DNA 1989; 2: 75–86
   Google Scholar
• Askin F B, Kuhn C. The cellular origin of pulmonary surfactant. Lab Invest 1971; 25: 260–8
   PubMed Web of Science ®Google Scholar
• King R J. The surfactant system of the lung. Fed Proc 1974; 33: 2238–47
   PubMedGoogle Scholar
• Goerke J. Lung surfactant. Biochim Biophys Acta 1975; 344: 241–61
   Google Scholar
• King R K, Klass D J, Gikas E G, Clements J A. Isolation of apoproteins from canine surface active material. Am J Physiol 1973; 224: 788–95
   PubMed Web of Science ®Google Scholar
• Klass D J. Immunochemical studies of the protein fraction of pulmonary surface active material. Am Rev Respir Dis 1973; 107: 784–9
   PubMed Web of Science ®Google Scholar
• Sueishi K, Tanake K, Oda T. Immunoultrastructural study of the surfactant system. Distribution of specific protein of surface active material in rabbit lung. Lab Invest 1977; 37: 136–42
   PubMed Web of Science ®Google Scholar
• Bhattacharyya S N. Characterization of collagenous and non-collagenous peptides of a glycoprotein isolated from alveoli of patients with alveolar proteinosis. Biochem J 1981; 193: 447–57
   PubMed Web of Science ®Google Scholar
• White R T, Damm D, Miller J, et al. Isolation and characterization of the human pulmonary surfactant apoprotein gene. Nature 1985; 317: 361–3
   PubMed Web of Science ®Google Scholar
• Warr R G, Hawgood S, Buckley D I, et al. Low molecular weight human pulmonary surfactant protein (SP5): Isolation, characterization, and cDNA and amino acid sequences. Proc Natl Acad Sci USA 1987; 84: 7915–19
   PubMed Web of Science ®Google Scholar
• Bruns G, Stroh H, Veldman G M, Latt S A, Floros J. The 35 kd pulmonary surfactant–associated protein is encoded on chromosome 10. Hum Genet 1987; 76: 58–62
   PubMed Web of Science ®Google Scholar
• Fisher J H, Kao F T, Jones C, White R T, Benson B J, Mason R J. The coding sequence for the 32,000-dalton pulmonary surfactant–associated protein A is located on chromosome 10 and identifies two separate restriction-fragment-length polymorphisms. Am J Hum Genet 1987; 40: 503–11
   PubMed Web of Science ®Google Scholar
• Glasser S W, Korfhagen T R, Weaver T, Pilot-Matias T, Fox J L, Whitsett J A. cDNA and deduced amino acid sequence of human pulmonary surfactant-associated proteolipid SPL(Phe). Proc Natl Acad Sci USA 1987; 84: 4007–11
   PubMed Web of Science ®Google Scholar
• Emrie P A, Jones C, Hofmann T, Fisher J H. The coding sequence for the human 18,000-dalton hydrophobic pulmonary surfactant protein is located on chromosome 2 and identifies a restriction fragment length polymorphism. Somat Cell Mol Genet 1988; 14: 105–10
   PubMedGoogle Scholar
• Glasser S W, Korfhagen T R, Weaver T E, et al. cDNA deduced polypeptide structure and chromosomal assignment of human pulmonary surfactant proteolipid SPL(pVal). J Biol Chem 1988; 263: 9–12
   PubMed Web of Science ®Google Scholar
• Moore K J, D'Amore-Bruno M A, Korfhagen T R, et al. Chromosomal localization of the three pulmonary surfactant protein genes in the mouse. Genomics 1992; 12: 388–93
   PubMedGoogle Scholar
• Weaver T E, Whitsett J A. Function and regulation of expression of pulmonary surfactant–associated proteins. Biochem J 1991; 273: 249–64
   PubMed Web of Science ®Google Scholar
• Haagsman H P, van Golde L MG. Synthesis and assembly of lung surfactant. Annu Rev Physiol 1991; 53: 441–64
   PubMed Web of Science ®Google Scholar
• Voorhout W F, Veenendaal T, Haagsman H P, et al. Intracellular processing of pulmonary surfactant protein B in an endosomal/lysosomal compartment. Am J Physiol 1992; 263: L479–86
   PubMedGoogle Scholar
• Coleman M, Dehner L P, Sibly R K, Burke B A, L'Heureux P R, Thompson T R. Pulmonary alveolar proteinosis: An uncommon cause of chronic neonatal respiratory distress. Am Rev Respir Dis 1980; 121: 583–6
   PubMedGoogle Scholar
• Knight D P, Knight J A. Pulmonary alveolar proteinosis in the newborn. Arch Pathol Lab Med 1985; 109: 529–31
   PubMedGoogle Scholar
• Schumacher R E, Marrogi A J, Heidelberger K P. Pulmonary alveolar proteinosis in a newborn. Pediatr Pulmonol 1989; 7: 178–82
   PubMedGoogle Scholar
• Nogee L M, deMello D E, Dehner L P, Colten H R. Brief report: Deficiency of pulmonary surfactant protein B in congenital alveolar proteinosis. N Engl J Med 1993; 328: 406–10
   PubMed Web of Science ®Google Scholar
• Nogee L M, Garnier G, Dietz H C, et al. A mutation in the surfactant protein B gene responsible for fatal neonatal respiratory distress in multiple kindreds. J Clin Invest 1994; 93: 1860–3
   PubMed Web of Science ®Google Scholar
• Hamvas A, Cole F S, deMello D E, et al. Surfactant protein deficiency: Antenatal diagnosis and prospective treatment with surfactant replacement. J Pediatr 1994; 125: 356–61
   PubMed Web of Science ®Google Scholar
• Phelps D S, Floros J. Localization of pulmonary surfactant proteins using immunohistochemistry and tissue in situ hybridization. Exp Lung Res 1991; 17: 985–95
   PubMed Web of Science ®Google Scholar