4.5 Article Proceedings Paper

Loss of Thy-1 inhibits alveolar development in the newborn mouse lung

Publisher

AMER PHYSIOLOGICAL SOC
DOI: 10.1152/ajplung.90603.2008

Keywords

transforming growth factor-beta; infant; CD90

Funding

  1. NCRR NIH HHS [C06 RR15490] Funding Source: Medline
  2. NHLBI NIH HHS [HL-007457, R01 HL092906, R01-HL-092906, HL-044195, HL-082818, HL-50147, HL-56046] Funding Source: Medline
  3. NICHD NIH HHS [K08-HD-046513] Funding Source: Medline

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Nicola T, Hagood JS, James ML, MacEwen MW, Williams TA, Hewitt MM, Schwiebert L, Bulger A, Oparil S, Chen Y, Ambalavanan N. Loss of Thy-1 inhibits alveolar development in the newborn mouse lung. Am J Physiol Lung Cell Mol Physiol 296: L738-L750, 2009. First published March 6, 2009; doi:10.1152/ajplung.90603.2008.-Transforming growth factor (TGF)-beta mediates hypoxia-induced inhibition of alveolar development in the newborn lung. TGF-beta is regulated primarily at the level of activation of latent TGF-beta. Fibroblasts expressing Thy-1 (CD90) inhibit TGF-beta activation. We hypothesized that loss of Thy-1 due to hypoxia may be a mechanism by which hypoxia increases TGF-beta activation and that animals deficient in Thy-1 will simulate the effects of hypoxia on lung development. To determine if loss of Thy-1 occurred during hypoxia, non-transgenic (C57BL/6) wild-type (WT) mice exposed to hypoxia were evaluated for Thy-1 mRNA and protein. To determine if Thy-1 deficiency simulated hypoxia, WT and Thy-1 null (Thy-1(-/-)) mice were exposed to air or hypoxia from birth to 2 wk, the critical period of lung development, and lung histology, function, parameters related to TGF-beta signaling, and extracellular matrix protein content were measured. To test if the phenotype in Thy-1(-/-) mice was due to excessive TGF-beta signaling, measurements were also performed in Thy-1(-/-) mice administered TGF-beta neutralizing antibody (1D11). We observed that hypoxia reduced Thy-1 mRNA and Thy-1 staining in WT mice. Thy-1(-/-) mice had impaired alveolarization, increased TGF-beta signaling, reduced lung epithelial and endothelial cell proliferation but increased fibroblast proliferation, and increased collagen and elastin. Lung compliance was lower, and tissue but not airway resistance was higher in Thy-1(-/-) mice at 2 wk. Thy-1(-/-) mice given 1D11 had improved alveolar development and lung function. These data support the hypothesis that hypoxia, by reducing Thy-1, increases TGF-beta activation, and thereby inhibits normal alveolar development.

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