Motheaten mice - An animal model with an inherited form of interstitial lung disease

G. A. Rossi, G. W. Hunninghake, O. Kawanami, V. J. Ferrans, C. T. Hansen, Ronald Crystal

Research output: Contribution to journalArticle

28 Citations (Scopus)

Abstract

The motheaten gene represents a single recessive mutation that occurs in mice and is associated with systemic immune abnormalities. Although they have abnormalities in several organs, homozygote animals (me/me) die by 8 wk of age from a diffuse, noninfectious lung disease. To evaluate this genetically determined model of interstitial lung disease, the lungs of these animals were studied by light and transmission electron microscopy and by bronchoalveolar lavage. Two control groups of mice were evaluated: (1) littermate normal mice, including mice without the motheaten gene (+/+) and mice heterozygous (me/+) the motheaten gene, and (2) nonlittermate normal mice (+/+). While the lungs of both control groups were normal morphologically, the lung disease in the homozygous motheaten mice progressed through 3 stages: (1) focal intra-alveolar hemorrhage with accumulations of alveolar macrophages and neutrophils in the lower respiratory tract; (2) persistent alveolitis and hemorrhage, and reparative processes including frequent mitoses of fibroblasts and type II alveolar epithelial cells; and (3) consolidation of the alveolar structures by massive accumulation of macrophages and marked derangement and fibrosis of the alveolar walls. Consistent with the morphologic findings, evaluation of mid-stage lung disease by lavage demonstrated that the alveolitis was characterized by a marked expansion of the total number of effector cells, an accumulation of neutrophils, and a marked expansion of the total number of T-lymphocytes and B-lymphocytes. Thus, the notheaten mouse can be regarded as a genetically determined model of interstitial lung disease characterized by alveolar hemorrhage, derangement of parenchymal cells, fibrosis, and an alveolitis with distinctive features. This mouse may be a useful model to follow the natural progression of interstitial lung disease of unknown origin and to help evaluate the pathogenesis of lung disorders associated with systemic immune abnormalities.

Original languageEnglish
Pages (from-to)150-158
Number of pages9
JournalAmerican Review of Respiratory Disease
Volume131
Issue number1
Publication statusPublished - 4 Apr 1985
Externally publishedYes

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Interstitial Lung Diseases
Animal Models
Lung Diseases
Bronchoalveolar Lavage
Hemorrhage
Lung
Neutrophils
Fibrosis
Genes
Animal Structures
Alveolar Epithelial Cells
Control Groups
Alveolar Macrophages
Homozygote
Transmission Electron Microscopy
Mitosis
Respiratory System
B-Lymphocytes
Fibroblasts
Cell Count

ASJC Scopus subject areas

  • Pulmonary and Respiratory Medicine

Cite this

Rossi, G. A., Hunninghake, G. W., Kawanami, O., Ferrans, V. J., Hansen, C. T., & Crystal, R. (1985). Motheaten mice - An animal model with an inherited form of interstitial lung disease. American Review of Respiratory Disease, 131(1), 150-158.

Motheaten mice - An animal model with an inherited form of interstitial lung disease. / Rossi, G. A.; Hunninghake, G. W.; Kawanami, O.; Ferrans, V. J.; Hansen, C. T.; Crystal, Ronald.

In: American Review of Respiratory Disease, Vol. 131, No. 1, 04.04.1985, p. 150-158.

Research output: Contribution to journalArticle

Rossi, GA, Hunninghake, GW, Kawanami, O, Ferrans, VJ, Hansen, CT & Crystal, R 1985, 'Motheaten mice - An animal model with an inherited form of interstitial lung disease', American Review of Respiratory Disease, vol. 131, no. 1, pp. 150-158.
Rossi GA, Hunninghake GW, Kawanami O, Ferrans VJ, Hansen CT, Crystal R. Motheaten mice - An animal model with an inherited form of interstitial lung disease. American Review of Respiratory Disease. 1985 Apr 4;131(1):150-158.
Rossi, G. A. ; Hunninghake, G. W. ; Kawanami, O. ; Ferrans, V. J. ; Hansen, C. T. ; Crystal, Ronald. / Motheaten mice - An animal model with an inherited form of interstitial lung disease. In: American Review of Respiratory Disease. 1985 ; Vol. 131, No. 1. pp. 150-158.
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