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Please use this identifier to cite or link to this item: http://repository.li.mahidol.ac.th/dspace/handle/123456789/16214
Title: Expression of liver-type fatty acid-binding protein in murine lung and its release into serum upon challenge of lung with lipopolysaccharide
Authors: Pattira Piumngam
Christian Schachtrup
Yuji Owada
Hisatake Kondo
Chamras Promptmas
Friedrich Spener
Westfalische Wilhelms-Universitat Munster
Mahidol University
Tohoku University
Karl-Franzens-Universitat Graz
Keywords: Agricultural and Biological Sciences;Biochemistry, Genetics and Molecular Biology;Chemistry;Engineering
Issue Date: 26-Apr-2005
Citation: European Journal of Lipid Science and Technology. Vol.107, No.3 (2005), 145-152
Abstract: Fatty acid-binding proteins (FABP) in alveolar type II (TII) cells are required for surfactant synthesis and regulation. Beyond expression of heart-type (H-) and epidermal-type (E-) FABP in TII cells from mouse lung, we present the first evidence of the expression of liver-type (L-) FABP, by quantitative PCR and immunofluorescent confocal laser microscopy. Further, by making use of an acute mouse lung injury model, we examine whether these lipid-binding proteins are released into the bronchoalveolar fluid (BALF) and into the circulation upon challenge of the lung with lipopolysaccharide. Applying FABP-specific ELISAs, we found that neither H- nor E-FABP can be detected in BALF and serum above background levels, up to 24 h after insult. In contrast, L-FABP was detected in the BALF pellet, consisting of polymorphonuclear cells and alveolar macrophages, and in serum. A significant decrease in L-FABP levels in the BALF pellet was associated with a significant increase in serum levels 6 h post insult. As contributions of L-FABP from other organs were excluded, this protein could be used as a marker for acute lung injury. © 2005 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
URI: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=17144388958&origin=inward
http://repository.li.mahidol.ac.th/dspace/handle/123456789/16214
ISSN: 14387697
Appears in Collections:Scopus 2001-2005

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