Ultrastructure of lamellar bodies in congenital surfactant deficiency

V. Edwards, E. Cutz, S. Viero, A. M. Moore, Lawrence Nogee

Research output: Contribution to journalArticle

Abstract

Congenital surfactant deficiency (CSD) is a newly identified neonatal lung disorder associated with a variety of molecular defects affecting surfactant synthesis and secretion in alveolar type II cells. The authors present ultrastructural findings of abnormal lamellar bodies in lung biopsies from 4 infants with CSD. All were term infants presenting shortly after birth with severe respiratory failure that was unresponsive to conventional therapy and all died within the first month of life. Lung biopsies were performed between 8 and 25 days of age. Biochemical and molecular studies in 2 unrelated male infants identified SP-B deficiency, one case with 121 ins 2 mutation and the second with a 209+4 A > G mutaion. Light microscopy in both cases showed features of alveolar proteinosis. Ultrastructurally, alveolar type II cells lacked mature lamellar bodies, and their cytoplasm contained numerous pleomorphic inclusions with membranous and vesicular structures not seen in normal type II cells. The other 2 infants were a pair of siblings in whom molecular studies identified mutations in ABCA3 transporter gene. Light microscopy showed features of acinar dysplasia and desquamative interstitial pneumonitis. TEM studies revealed absence of mature lamellar bodies in type II cells and instead showed a mixture of cytoplsamic electron-dense inclusions with concentric membranes and distinctive electron dense aggregates. The ultrastructual changes in alveolar type II cells correlated well with specific gene defect. In SP-B deficiency, the absence of mature lamellar bodies is consistent with the postulated role for this protein in the formation of lamellar bodies. The lack of mature lamellar bodies in the ABCA3 gene mutations is due to the dysfunction of this endogenous lipid transporter that targets surfactant lipid moieties to the lamellar bodies. The findings demonstrate the importance of TEM studies of lung biopsies from infants with CSD as it is a critical adjunct in the diagnosis of neonatal lung disease and in defining the underlying cellular defects.

Original languageEnglish (US)
Pages (from-to)503-509
Number of pages7
JournalUltrastructural Pathology
Volume29
Issue number6
DOIs
StatePublished - Nov 2005

Fingerprint

Surface-Active Agents
Surface active agents
Alveolar Epithelial Cells
surfactants
Biopsy
lungs
Lung
Genes
mutations
genes
Defects
Lipids
Mutation
transporter
Optical microscopy
cells
Infant, Newborn, Diseases
Microscopy
Electrons
Transmission electron microscopy

Keywords

  • ABCA3 mutations
  • Alveolar type II cells
  • Respiratory failure in term neonates
  • SP-B deficiency

ASJC Scopus subject areas

  • Pathology and Forensic Medicine
  • Instrumentation
  • Structural Biology

Cite this

Ultrastructure of lamellar bodies in congenital surfactant deficiency. / Edwards, V.; Cutz, E.; Viero, S.; Moore, A. M.; Nogee, Lawrence.

In: Ultrastructural Pathology, Vol. 29, No. 6, 11.2005, p. 503-509.

Research output: Contribution to journalArticle

Edwards, V. ; Cutz, E. ; Viero, S. ; Moore, A. M. ; Nogee, Lawrence. / Ultrastructure of lamellar bodies in congenital surfactant deficiency. In: Ultrastructural Pathology. 2005 ; Vol. 29, No. 6. pp. 503-509.
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