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Characterization of spontaneous air space enlargement in mice lacking microfibrillar-associated protein 4.
Am. J. Physiol. Lung Cell Mol. Physiol. 308, L1114-L1124 (2015)
DOI
online verfügbar vsl. 04/2016 
Microfibrillar-associated protein 4 (MFAP4) is localized to elastic fibers in blood vessels and the interalveolar septa of the lungs and is further present in bronchoalveolar lavage. Mfap4 has been previously suggested to be involved in elastogenesis in the lung. We tested this prediction and aimed to characterize the pulmonary function changes and emphysematous changes that occur in Mfap4 deficient (Mfap4-/-) mice. Significant changes included increases in total lung capacity and compliance, which were evident in Mfap4-/- mice at 6 months and 8 months, but not at 3 months of age. Using in vivo breath-hold gated micro-computed tomography (micro-CT) in 8-month-old Mfap4-/- mice, we found that the mean density of the lung parenchyma was decreased, and the low-attenuation area (LAA) was significantly increased by 14 % compared to Mfap4+/+ mice. Transmission electron microscopy (TEM) did not reveal differences in the organization of elastic fibers, and there was no difference in elastin content, but borderline significant increase in elastin mRNA expression in 3-month-old mice. Stereological analysis showed that alveolar surface density in relation to the lung parenchyma and total alveolar surface area inside of the lung were both significantly decreased in Mfap4-/- mice by 25 % and 15 %, respectively. The data did not support an essential role of MFAP4 in pulmonary elastic fiber organization or content, but indicated increased turnover in young Mfap4-/- mice. However, Mfap4-/- mice developed a spontaneous loss of lung function, which was evident at 6 months of age, and moderate airspace enlargement, with emphysema-like changes.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Wissenschaftlicher Artikel
Schlagwörter Mfap4 ; Air Space Enlargement ; Gene Deficiency; Obstructive Pulmonary-disease; Elastase-induced Emphysema; Computed-tomography; Glycoprotein Magp-36; Lung Morphology; Binding Protein; Gene-expression; Murine Model; Localization; Progression
ISSN (print) / ISBN 1040-0605
e-ISSN 1522-1504
Zeitschrift American Journal of Physiology - Lung Cellular and Molecular Physiology
Quellenangaben Band: 308, Heft: 11, Seiten: L1114-L1124 Artikelnummer: , Supplement: ,
Verlag American Physiological Society
Verlagsort Bethesda, Md. [u.a.]
Begutachtungsstatus peer-reviewed