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Publication : Restoration of PPARγ reverses lipid accumulation in alveolar macrophages of GM-CSF knockout mice.

First Author  Malur A Year  2011
Journal  Am J Physiol Lung Cell Mol Physiol Volume  300
Issue  1 Pages  L73-80
PubMed ID  21036914 Mgi Jnum  J:168397
Mgi Id  MGI:4888159 Doi  10.1152/ajplung.00128.2010
Citation  Malur A, et al. (2011) Restoration of PPARgamma reverses lipid accumulation in alveolar macrophages of GM-CSF knockout mice. Am J Physiol Lung Cell Mol Physiol 300(1):L73-80
abstractText  Pulmonary alveolar proteinosis (PAP) is a lung disease characterized by a deficiency of functional granulocyte macrophage colony-stimulating factor (GM-CSF) resulting in surfactant accumulation and lipid-engorged alveolar macrophages. GM-CSF is a positive regulator of PPARgamma that is constitutively expressed in healthy alveolar macrophages. We previously reported decreased PPARgamma and ATP-binding cassette transporter G1 (ABCG1) levels in alveolar macrophages from PAP patients and GM-CSF knockout (KO) mice, suggesting PPARgamma and ABCG1 involvement in surfactant catabolism. Because ABCG1 represents a PPARgamma target, we hypothesized that PPARgamma restoration would increase ABCG1 and reduce macrophage lipid accumulation. Upregulation of PPARgamma was achieved using a lentivirus expression system in vivo. GM-CSF KO mice received intratracheal instillation of lentivirus (lenti)-PPARgamma or control lenti-eGFP. Ten days postinstillation, 79% of harvested alveolar macrophages expressed eGFP, demonstrating transduction. Alveolar macrophages showed increased PPARgamma and ABCG1 expression after lenti-PPARgamma instillation, whereas PPARgamma and ABCG1 levels remained unchanged in lenti-eGFP controls. Alveolar macrophages from lenti-PPARgamma-treated mice also exhibited reduced intracellular phospholipids and increased cholesterol efflux to HDL, an ABCG1-mediated pathway. In vivo instillation of lenti-PPARgamma results in: 1) upregulating ABCG1 and PPARgamma expression of GM-CSF KO alveolar macrophages, 2) reducing intracellular lipid accumulation, and 3) increasing cholesterol efflux activity.
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