Mitochondrial Components Are a Possible Trigger of Auto-inflammatory Illnesses
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BOSTON (December 17, 2012) — Many illnesses, including psoriasis, include inflammatory responses that occur without an apparent infection and worsen with stress. In a study using cultured human mast cells in vitro and in rats, researchers from Tufts University School of Medicine and the Sackler School of Graduate Biomedical Sciences at Tufts University identified mitochondrial particles — secreted from live, activated mast cells — as a possible trigger of the inflammation that is common in such illnesses.
Mast cells are a part of the immune system and can secrete inflammatory molecules, such as histamine, in response to allergens and other triggers. Generated in the bone marrow, mast cells play vital roles in acquired and innate immunity within tissues in the body. Little is known about their secretory process except that energy generated by mitochondria is required.
When a person contracts an infection or has an allergic reaction, mast cells normally secrete molecules that alert the immune system to the presence of a foreign invader. These molecules trigger the body’s responses in order to contain and eliminate the infection or alert the body to initiate an inflammatory response. After this process, the mast cell regenerates. The research team sought to understand how inflammation could be triggered without the presence of an infection or allergen.
In the study, mast cells were stimulated by triggers secreted from nerves, rather than by infection or allergen. As a result, the mast cells secreted their inflammation-causing molecules, as well as some mitochondrial components. The mitochondrial components were secreted outside the cell into the extracellular fluid, but the mast cells retained their viability, indicating that the secretion of mitochondrial particles was not due to cell damage or death. The extracellular mitochondrial components then stimulated other skin cells to mount an auto-inflammatory response.
Purified human mitochondrial components were also injected into peripheral tissue of rats. Within four hours, they were detected in the blood, which suggests that mitochondrial components secreted in tissues can reach the systemic circulation, the part of the cardiovascular system that carries blood from the heart to the rest of the body.
“The immune system misread the mitochondrial components as an infectious agent, and there was inflammation as a result,” said first author Bodi Zhang, M.D., M.P.H., Ph.D., graduate of the biochemistry program at the Sacker School. “Our study findings are different from a report last year suggesting that mitochondrial particles are released from damaged cells in patients with severe trauma. Additional studies are needed to gain a better understanding of this process.”
“Our work provides a possible explanation for inflammation that arises without apparent disease or injury,” said senior author Theoharis C. Theoharides, M.S., Ph.D., M.D., professor of molecular physiology and pharmacology at Tufts University School of Medicine and member of the Biochemistry, and Pharmacology & Experimental Therapeutics graduate program faculties at the Sackler School. “Secretion of mitochondrial components by immune cells may constitute an ‘innate pathogen’ that may stimulate self-response by the immune system.”
“Although this study does not identify the inflammatory mechanism that is common among auto-inflammatory illnesses, the findings help to lay a foundation for further research and may lead to new biomarkers and novel treatment targets,” Theoharides added.
This research was supported in part by grants to Theoharides from the National Institute of Arthritis and Musculoskeletal and Skin Diseases of the National Institutes of Health under award number R01AR47652 and by Safe Minds. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. Tufts University has filed a patent application related to these findings.
Additional authors on the study are Shahrzad Asadi, Pharm.D., postdoctoral scholar in the Theoharides laboratory; Zuyi Weng, B.S., graduate student in the Pharmacology & Experimental Therapeutics program at the Sackler School working in Dr. Theoharides’ laboratory; and Nikolaos Sismanopoulos, M.D., formerly a postdoctoral fellow in the Theoharides’ laboratory and now at St. Elizabeth’s Medical Center. The authors have declared that no competing interests exist.
Zhang B., Asadi S., Weng Z., Sismanopoulos N., Theoharides, T.C. (2012). Stimulated Human Mast Cells Secrete Mitochondrial Components That Have Autocrine and Paracrine Inflammatory Actions. PLoS ONE 7(12): e49767. doi:10.1371/journal.pone.0049767.
About Tufts University School of Medicine and the Sackler School of Graduate Biomedical Sciences
Tufts University School of Medicine and the Sackler School of Graduate Biomedical Sciences at Tufts University are international leaders in innovative medical and population health education and advanced research. Tufts University School of Medicine emphasizes rigorous fundamentals in a dynamic learning environment to educate physicians, scientists, and public health professionals to become leaders in their fields. The School of Medicine and the Sackler School are renowned for excellence in education in general medicine, the biomedical sciences, and public health, as well as for innovative research at the cellular, molecular, and population health level. Ranked among the top in the nation, the School of Medicine is affiliated with six major teaching hospitals and more than 30 health care facilities. Tufts University School of Medicine and the Sackler School undertake research that is consistently rated among the highest in the nation for its effect on the advancement of medical and prevention science.
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