Rheumatoid arthritis is a common inflammatory joint disease. A feature of this disease is the increased fusion of endogenous immune cells (macrophages) to form so-called osteoclasts, which attack and break down bone tissue.
Just like other multinuclear giant cells, osteoclasts require enhanced energy metabolism for bone breakdown. The findings of this study now demonstrate that increases in osteoclast metabolism cannot be achieved in the absence of arginine.
The group led by Gernot Schabbauer from MedUni Vienna, head of the Christian Doppler Laboratory for Arginine Metabolism, has now shown in various animal models that systemically depleting arginine in the body slows down the metabolism of these giant cells, significantly diminishing their function. To achieve this, the researchers used the enzyme arginase, which lowers whole-body arginine levels. This resulted in decreased osteoclasts numbers in the bone, therefore leading to less disease instigated damage.
“Although arginine is an endogenous substance, it is also supplemented by diet,” explains first author Julia Brunner, “our results indicate that osteoclast formation and metabolism could be slowed down by restricting arginine in the body.”
Arginine is an amino acid that is semi-essential, i.e., although it can be synthesized by the body’s own metabolic pathways, it has to be as well supplied by diet. “Arginine can act like a fuel for cells and essentially has several beneficial effects,” explains Brunner, “however, in pathological situations, its presence can cause T-cells to overreact or lead to undesirable increases in cell numbers.”
These reactions can be restricted by the arginine-degrading enzyme arginase. “Arginase is part of the urea cycle in the liver, but also operates in immune cells and, hence, can act as a regulator for arginine,” explains Principal Investigator Gernot Schabbauer from MedUni Vienna’s Institute of Vascular Biology and Thrombosis Research. “Arginine also plays an important role in the growth and development of immune cells that operate in auto-immune diseases such as multiple sclerosis. Arginase is therefore not only a highly promising starting point for the development of new treatment options for rheumatoid arthritis, but it might also be important for other autoimmune diseases.”
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