Pulmonary hypoplasia in the myogenin null mouse embryo

Brian S. Tseng, Sash T. Cavin, Frank W. Booth, Eric N. Olson, Maria Carmen Marin, Timothy J. McDonnell, Ian J. Butler

Research output: Contribution to journalArticle

35 Citations (Scopus)

Abstract

Although fetal breathing movements are required for normal lung development, there is uncertainty concerning the specific effect of absent fetal breathing movements on pulmonary cell maturation. We set out to evaluate pulmonary development in a genetically defined mouse model, the myogenin null mouse, in which there is a lack of normal skeletal muscle fibers and thus skeletal muscle movements are absent in utero. Significant decreases were observed in lung:body weight ratio and lung total DNA at embryonic days (E)14, E17, and E20. Reverse transcriptase/polymerase chain reaction, in situ immunofluorescence, and electron microscopy revealed early lung cell differentiation in both null and wild-type lungs as early as E14. However at E14, myogenin null lungs had decreased 5'-bromo-2-deoxyuridine incorporation compared with that of wild-type littermates, whereas at E17 and E20, increased Bax immunolabeling and terminal deoxyribonucleotidyl transferase-mediated dUTP-biotin nick-end labeling staining were detected in the myogenin null mice but not in the wild-type littermates. These observations highlight the importance of skeletal muscle contractile activity in utero for normal lung organogenesis. Null mice lacking the muscle-specific transcription factor myogenin exhibit a secondary effect on lung development such that decreased lung cell proliferation and increased programmed cell death are associated with lung hypoplasia.

Original languageEnglish (US)
Pages (from-to)304-315
Number of pages12
JournalAmerican Journal of Respiratory Cell and Molecular Biology
Volume22
Issue number3
StatePublished - 2000

Fingerprint

Myogenin
Muscle
Embryonic Structures
Lung
DNA Nucleotidylexotransferase
Polymerase chain reaction
RNA-Directed DNA Polymerase
Cell proliferation
Cell death
Bromodeoxyuridine
Biotin
Labeling
Electron microscopy
Fetal Movement
Transcription Factors
Fibers
DNA
Respiration
Skeletal Muscle
Organogenesis

ASJC Scopus subject areas

  • Cell Biology
  • Pulmonary and Respiratory Medicine
  • Molecular Biology

Cite this

Tseng, B. S., Cavin, S. T., Booth, F. W., Olson, E. N., Marin, M. C., McDonnell, T. J., & Butler, I. J. (2000). Pulmonary hypoplasia in the myogenin null mouse embryo. American Journal of Respiratory Cell and Molecular Biology, 22(3), 304-315.

Pulmonary hypoplasia in the myogenin null mouse embryo. / Tseng, Brian S.; Cavin, Sash T.; Booth, Frank W.; Olson, Eric N.; Marin, Maria Carmen; McDonnell, Timothy J.; Butler, Ian J.

In: American Journal of Respiratory Cell and Molecular Biology, Vol. 22, No. 3, 2000, p. 304-315.

Research output: Contribution to journalArticle

Tseng, BS, Cavin, ST, Booth, FW, Olson, EN, Marin, MC, McDonnell, TJ & Butler, IJ 2000, 'Pulmonary hypoplasia in the myogenin null mouse embryo', American Journal of Respiratory Cell and Molecular Biology, vol. 22, no. 3, pp. 304-315.
Tseng BS, Cavin ST, Booth FW, Olson EN, Marin MC, McDonnell TJ et al. Pulmonary hypoplasia in the myogenin null mouse embryo. American Journal of Respiratory Cell and Molecular Biology. 2000;22(3):304-315.
Tseng, Brian S. ; Cavin, Sash T. ; Booth, Frank W. ; Olson, Eric N. ; Marin, Maria Carmen ; McDonnell, Timothy J. ; Butler, Ian J. / Pulmonary hypoplasia in the myogenin null mouse embryo. In: American Journal of Respiratory Cell and Molecular Biology. 2000 ; Vol. 22, No. 3. pp. 304-315.
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