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(18)F-Labeling of Mannan for Inflammation Research with Positron Emission Tomography.


ABSTRACT: Recently mannan from Saccharomyces cerevisiae has been shown to be able to induce psoriasis and psoriatic arthritis in mice, and the phenotypes resemble the corresponding human diseases. To investigate the pathological processes, we set out to label mannan with fluorine-18 ((18)F) and study the (18)F-labeled mannan in vitro and in vivo with positron emission tomography (PET). Accordingly, mannan has been transformed into (18)F-fluoromannan with (18)F-bicyclo[6.1.0]nonyne. In mouse aorta, the binding of [(18)F]fluoromannan to the atherosclerotic lesions was clearly visualized and was significantly higher compared to blocking assays (P < 0.001) or healthy mouse aorta (P < 0.001). In healthy rats the [(18)F]fluoromannan radioactivity accumulated largely in the macrophage-rich organs such as liver, spleen, and bone marrow and the excess excreted in urine. Furthermore, the corresponding (19)F-labeled mannan has been used to induce psoriasis and psoriatic arthritis in mice, which indicates that the biological function of mannan is preserved after the chemical modifications.

SUBMITTER: Li XG 

PROVIDER: S-EPMC5018871 | biostudies-other | 2016 Sep

REPOSITORIES: biostudies-other

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(18)F-Labeling of Mannan for Inflammation Research with Positron Emission Tomography.

Li Xiang-Guo XG   Hagert Cecilia C   Siitonen Riikka R   Virtanen Helena H   Sareila Outi O   Liljenbäck Heidi H   Tuisku Jouni J   Knuuti Juhani J   Bergman Jörgen J   Holmdahl Rikard R   Roivainen Anne A  

ACS medicinal chemistry letters 20160516 9


Recently mannan from Saccharomyces cerevisiae has been shown to be able to induce psoriasis and psoriatic arthritis in mice, and the phenotypes resemble the corresponding human diseases. To investigate the pathological processes, we set out to label mannan with fluorine-18 ((18)F) and study the (18)F-labeled mannan in vitro and in vivo with positron emission tomography (PET). Accordingly, mannan has been transformed into (18)F-fluoromannan with (18)F-bicyclo[6.1.0]nonyne. In mouse aorta, the bin  ...[more]

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