Medizinische Universität Graz Austria/Österreich - Forschungsportal - Medical University of Graz
Gewählte Publikation:
SHR Neuro Krebs Kardio Lipid Stoffw Microb
Schachtrup, C; Malcharek, S; Haitsma, JJ; Lachmann, B; Owada, Y; Binas, B; Kondo, H; Rüstow, B; Galla, HJ; Spener, F.
Activation of PPARgamma reverses a defect of surfactant synthesis in mice lacking two types of fatty acid binding protein.
Biochim Biophys Acta. 2008; 1781(6-7):314-320
Doi: 10.1016/j.bbalip.2008.04.010
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- Co-Autor*innen der Med Uni Graz
- Spener Friedrich
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- Abstract:
- Lung surfactant is a lipid-protein-film covering the inner alveolar surface. We have previously shown that double knock-out (d-ko) mice lacking both the epidermal-type (E-) and the heart-type (H-) fatty acid binding protein (FABP) exhibit a defect of surfactant synthesis in alveolar type II cells that can be corrected by feeding pioglitazone, a drug that activates peroxisome proliferator-activated receptor gamma (PPARgamma). Here, we demonstrate first that healthy surfactant at collapse pressure produces protrusions composed of bilayers but not folds, second that the d-ko effect profoundly perturbs lipid/hydrophobic protein composition, pressure-area isotherm, and structural organisation of the surfactant at nanoscale, parameters that are critical for the normal breathing cycle. In support of these data in vivo measurements of lung function reveal that maximum compliance in d-ko vs. wild-type mice is significantly reduced. Further, we show that the biophysical phenotype can be corrected substantially with pioglitazone. Finally, we show that d-ko alveolar cells up-regulate liver-type (L-) FABP, a member of the FABP family that we have previously shown to interact with PPARgamma. Taken together, these data suggest that PPARgamma agonists could be a tool to repair surfactant damage caused by dysfunctional alveolar lipid metabolism, and provide in vivo support for L-FABP aided signaling.
- Find related publications in this database (using NLM MeSH Indexing)
- Animals -
- Base Sequence -
- DNA Primers -
- Enzyme-Linked Immunosorbent Assay -
- Fatty Acid-Binding Proteins - genetics
- Hypoglycemic Agents - pharmacology
- Mice -
- Mice, Inbred C57BL -
- Mice, Knockout -
- PPAR gamma - agonists
- Pulmonary Surfactants - metabolism
- Thiazolidinediones - pharmacology
- Find related publications in this database (Keywords)
- phospholipid synthesis
- fatty acid binding protein
- fatty acid signaling
- surfactant organisation
- lung compliance