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Structural Characterization of Mannan Cell Wall Polysaccharides in Plants Using PACE
Published on: October 16, 2017
Rapid spread of mannan to the immune system, skin and joints within 6 hours after local exposure
C Hagert1,2, R Siitonen3, X-G Li3,4
1Medical Inflammation Research, MediCity Research Laboratory, University of Turku, Turku, Finland.
Abstract:
Psoriasis (Ps), psoriatic arthritis (PsA) and rheumatoid arthritis (RA) are common diseases dependent on environmental factors that activate the immune system in unknown ways. Mannan is a group of polysaccharides common in the environment; they are potentially pathogenic, because at least some of them induce Ps-, PsA- and RA-like inflammation in mice. Here, we used positron emission tomography/computed tomography to examine in-vivo transport and spread of mannan labelled with fluorine-18 [18 F]. The results showed that mannan was transported to joints (knee) and bone marrow (tibia) of mice within 6 h after intraperitoneal injection. The time it took to transport mannan, and its presence in blood, indicated cellular transport of mannan within the circulatory system. In addition, mannan was filtered mainly through the spleen and liver. [18 F]fluoromannan was excreted via kidneys, small intestine and, to some extent, the mouth. In conclusion, mannan reaches joints rapidly after injection, which may explain why mannan-induced inflammatory disease is targeted to these tissues.
Insights
Mannan, a common environmental polysaccharide, rapidly travels to joints and bone marrow after injection. This rapid transport may explain how mannan triggers inflammatory diseases like psoriasis and arthritis.
Area of Science:
- Immunology
- Biochemistry
- Medical Imaging
Background:
- Psoriasis (Ps), psoriatic arthritis (PsA), and rheumatoid arthritis (RA) are common inflammatory diseases.
- Environmental factors are implicated in disease activation, but mechanisms remain unclear.
- Mannan, a polysaccharide found in the environment, can induce Ps-, PsA-, and RA-like inflammation in mice.
Purpose of the Study:
- To investigate the in-vivo transport and distribution of mannan in mice.
- To understand the pathways of mannan uptake and excretion.
Main Methods:
- Fluorine-18 ([18F])-labeled mannan was synthesized.
- Positron emission tomography/computed tomography (PET/CT) was used to track [18F]fluoromannan distribution.
- Mice received intraperitoneal injections of [18F]fluoromannan.
Main Results:
- Mannan was rapidly transported to joints (knee) and bone marrow (tibia) within 6 hours post-injection.
- Presence in blood and rapid distribution suggested cellular transport via the circulatory system.
- Mannan was primarily filtered by the spleen and liver.
- [18F]fluoromannan was excreted through the kidneys, small intestine, and mouth.
Conclusions:
- Mannan rapidly reaches joint tissues after administration.
- The rapid joint targeting of mannan provides a potential explanation for its role in inducing localized inflammatory diseases in these tissues.
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