Pathologists have known about the existence of multinucleated giant cells (MGCs) for over a century. The cells occur in certain chronic inflammatory diseases, such as tuberculosis, but also during the foreign body reaction to implants, such as an artificial hip. Still, systematic research into the exact functions and abilities of MGCs remained scarce and left many questions open. “Because they are so big and derive from multiple phagocytic cells, it had been suggested that they may act as specialized disposal units for particular forms of waste. But a definitive confirmation or a molecular and cellular basis for this theory was so far lacking,” explained Dr. Admar Verschoor, co-author of the study and group leader at the TUM’s Institute for Medical Microbiology, Immunology and Hygiene.
Systemic amyloidosis as a model system
To investigate the function of the giant cells, he and his team conducted a series of sophisticated cell culture experiments, while at the same time also looking into systemic amyloidosis, a disease in which extensive protein deposits gradually disrupt the function of affected organs, such as the liver or spleen. The team joined forces with Mark B. Pepys, a leading amyloidosis researcher from the University College London. In clinical trials, Pepys had already successfully tested a new treatment against the disease, which among other things promotes the formation of giant cells.
“The treatment´s exact mode of action remained still unclear in several regards. It turned out to be a perfect setting to apply our expertise in phagocytic cells and the immune system, and to more precisely examine how giant cells function,” remarked Ronny Milde, the study’s lead author and scientist at TUM. Using the combination of cell culture experiments and the amyloidosis disease model, the researchers were able to give the amyloidosis treatment a mechanistic basis, revealing how giant cells get a little help from something called the "complement system" in picking up the bulky and disruptive protein deposits.
Giant cells dispose of bulky waste
“Complement acts a bit like the butter on our bread; Just like bread tastes better with a bit of butter on it, the pathogenic protein deposits in amyloidosis become more attractive for giant cells with a bit of complement on them. Besides promoting the formation of giant cells, the new treatment also leads to complement deposition onto the amyloid deposits,” explained Admar Verschoor. The researchers observed under the microscope how the large phagocytic cells surround and destroy the disruptive protein clumps. “Our studies show that giant cells are particularly well suited to remove large targets that are complement-marked, explaining why they can act so effectively in the promising new treatment for systemic amyloidosis,” pointed out Verschoor.
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Ronny Milde, Julia Ritter, Glenys A. Tennent, Andrzej Loesch, Fernando O. Martinez, Siamon Gordon, Mark B. Pepys, Admar Verschoor, Laura Helming, Multinucleated giant cells are specialized for complement-mediated phagocytosis and large target destruction, Cell Reports, November 2015.
Admar Verschoor, PhD
Institute for Medical Microbiology, Immunology and Hygiene
The “Klinikum rechts der Isar” of the Technical University of Munich
Tel.: +49 89 4140-6720