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• W2003744390 abstract "Immunohistochemistry (IHC) and in situ hybridization (ISH) was used to localize extracellular superoxide dismutase (EC-SOD) and its mRNA in rat lung before and after a lipopolysaccharide (LPS)- and hyperoxia-induced inflammation. In control rats, EC-SOD mRNA was synthesized in macrophages and in cells of the arterial vessel walls and the alveolar septa. The EC-SOD protein was mainly localized in plasma and on the apical side of the epithelial cells located near bronchus-associated lymphoid tissue (BALT). ISH did not reveal major changes in the distribution of EC-SOD mRNA upon induction of inflammation. In contrast, IHC demonstrated a progressive staining of the epithelium of the larger bronchi for the protein. Neutrophils and macrophages invading the lung showed an intensive staining for the EC-SOD protein concomitantly with a decrease of the enzyme in the plasma. Twenty-four hours after LPS stimulation only a spotty positivity remained on neutrophils in and between the alveolar spaces. In the bronchoalveolar lavage fluid (BALF), only macrophages showed a strong positivity for EC-SOD mRNA while the protein was detected in macrophages and neutrophils. Exposure to hyperoxia did not affect the distribution of EC-SOD mRNA and protein. The presented data demonstrated that in lung tissue the EC-SOD enzyme may have a protective function for activated macrophages, neutrophils, and lympoid tissue-associated epithelial cells." @default.
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• W2003744390 date "1998-05-01" @default.
• W2003744390 modified "2023-10-18" @default.
• W2003744390 title "Localization of Extracellular Superoxide Dismutase in Rat Lung: Neutrophils and Macrophages as Carriers of the Enzyme" @default.
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• W2003744390 doi "https://doi.org/10.1016/s0891-5849(97)00434-6" @default.
• W2003744390 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/9626563" @default.
• W2003744390 hasPublicationYear "1998" @default.
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