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Peroxisome proliferators alter lipid acquisition and elastin gene expression in neonatal rat lung fibroblasts
Journal article   Open access   Peer reviewed

Peroxisome proliferators alter lipid acquisition and elastin gene expression in neonatal rat lung fibroblasts

Stephen E McGowan, Sheila K Jackson, Melissa M Doro and Paula J Olson
The American journal of physiology, Vol.273(6), pp.L1249-L1257
12/1997
DOI: 10.1152/ajplung.1997.273.6.L1249
PMID: 9435581
url
https://doi.org/10.1152/ajplung.1997.273.6.L1249View
Published (Version of record) Open Access

Abstract

During the alveolar stage of lung development, lipid droplet-laden interstitial cells are present at the base of elongating alveolar septa. These cells that have been named lipid interstitial cells or lipofibroblasts (LFs) may supply lipids for surfactant production, the synthesis of membrane phospholipids, and/or energy metabolism. They also have myofibroblastic characteristics and participate in the generation of the interstitial elastic fiber network, that is, in the pulmonary alveolar septum. To understand how this cell regulates its lipid-storing and elastin-producing properties, we have examined the effects of peroxisome proliferators on the expression of the genes that are associated with an elastin-producing myofibroblastic phenotype or an adipocyte-like phenotype. Two known ligands for peroxisome proliferator-activated receptors, 5,8,11,14-eicosatetraynoic acid (ETYA) and 15-deoxy-delta-12,14-prostaglandin J2 (15-dPGJ2), decrease elastin gene transcription and the steady-state levels of tropoelastin (TE) and alpha-smooth muscle actin mRNAs in cultured LFs. Concurrently, cultured LFs increase the expression of adipocyte lipid binding protein, which is regarded as an adipocyte-specific protein, and accumulate lipid droplets. Their abilities to store lipids and express desmin intermediate filaments, alpha-smooth muscle actin, and smooth muscle myosin heavy chain in contractile filaments in vitro illustrate similarities among the pulmonary LF, the hepatic lipocyte, and the contractile interstitial cell, which contribute to the repair reaction in the lung after pulmonary injury.
Lipid Metabolism Animals, Newborn Recombinant Fusion Proteins - biosynthesis Transcription, Genetic - drug effects Transcription Factors - physiology Actins - biosynthesis Cells, Cultured Microbodies - drug effects Rats Receptors, Cytoplasmic and Nuclear - physiology 5,8,11,14-Eicosatetraynoic Acid - pharmacology Lung - cytology Gene Expression Regulation - drug effects RNA, Messenger - biosynthesis Animals Fibroblasts - drug effects Elastin - biosynthesis Prostaglandin D2 - analogs & derivatives Fibroblasts - cytology Lung - metabolism Prostaglandin D2 - pharmacology Cytoskeletal Proteins - biosynthesis Fibroblasts - metabolism

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