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Infect. Immun., May 1995, 1652-1657, Vol 63, No. 5
MA Hoijer, MJ Melief, CG van Helden-Meeuwsen, F Eulderink and MP Hazenberg
In previous studies, we showed that peptidoglycan polysaccharides from
anaerobic bacteria normally present in the human gut induced severe chronic
joint inflammation in rats. Our hypothesis is that peptidoglycan from the
gut flora is involved in perpetuation of idiopathic inflammation. However,
in the literature, the presence of peptidoglycan or subunits like muramyl
peptides in blood or tissues is still a matter of debate. We were able to
stain red pulp macrophages in all six available human spleens by
immunohistochemical techniques using a monoclonal antibody against gut
flora-derived antigens. Therefore, these human spleens were extracted, and
after removal of most of the protein, the carbohydrate fraction was
investigated for the presence of muramic acid, an amino sugar
characteristic for peptidoglycan. Using three different methods for
detection of muramic acid, we found a mean of 3.3 mumol of muramic acid
with high-pressure liquid chromatography, 1.9 mumol with a colorimetric
method for detection of lactate, and 0.8 mumol with an enzymatic method for
detection of D-lactate per spleen (D- lactate is a specific group of the
muramic acid molecule). It is concluded that peptidoglycan is present in
human spleen not as small muramyl peptides as were previously searched for
by other investigators but as larger macromolecules probably stored in
spleen macrophages.
Copyright © 1995, American Society for Microbiology
Detection of muramic acid in a carbohydrate fraction of human spleen
Department of Immunology, Erasmus University, Rotterdam, The Netherlands.
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