Phagocytes are the white blood cells that protect the body by eating (phagocytosing) dirt, bacteria and dead or dying cells. They are important for fighting infections. They are also important for becoming immune. Phagocytes are important in all animals and are very complex in vertebrates. One liter of human blood has about six billion phagocytes.
History[change | change source]
Their name comes from the Greek phagein, 'to eat or devour ', and kutos, 'hollow vessel'. Phagocytes were first seen in 1882 by Ilya Ilyich Mechnikov. Phagocytes can be found in many animals. Some amoebae behave like macrophages, and scientists think macrophages evolved a long time ago.
Professional phagocyte[change | change source]
Phagocytes of humans and other animals are called professional or non-professional, depending on how good they are at phagocytosis. The professional phagocytes are neutrophils, monocytes, macrophages, dendritic cells, and mast cells. The reason they are called professional phagocytes is because they have receptors on their surfaces which can detect harmful objects, such as bacteria. Phagocytes are very important in fighting infections and in getting rid of dead and dying cells.
What a phagocyte does[change | change source]
When there is an infection, phagocytes move to the bacteria by sensing chemicals. These chemicals may come from bacteria or from other phagocytes that are already there. The phagocytes move by a way called chemotaxis. When bacteria touch a phagocyte, they bind to the receptors on the phagocyte and are eaten (phagocytosed). When bacteria enter some phagocytes, the phagocytes use oxidants and nitric oxide to kill the pathogen. After phagocytosis, macrophages and dendritic cells can also do 'antigen presentation': this is when the phagocyte moves parts of the killed bacteria back to its surface. These parts are then shown to other cells of the immune system. Some phagocytes then move to the body's lymph nodes and show the bacterial parts to white blood cells called lymphocytes. This action is important in getting immunity.
Many bacteria now have ways to not be eaten or killed by phagocytes.
References[change | change source]
- Mayer, Gene (2006). "Immunology — Chapter One: Innate (non-specific) Immunity". Microbiology and Immunology On-Line Textbook. USC School of Medicine. http://pathmicro.med.sc.edu/ghaffar/innate.htm. Retrieved November 12, 2008.
- Delves P.J. et al 2006. Roitt's essential immunology. 11th ed, Malden, MA: Blackwell, p. 250/1. ISBN 1-4051-3603-0
- Hoffbrand A.V; Pettit J.E. & Moss P.A.H. 2005. Essential haematology. 4th ed, London: Blackwell, p. 331. ISBN 0-632-05153-1
- The Shorter Oxford English Dictionary. Oxford University Press (Guild Publishing). 1983. pp. 1566–67.
- Ilya Mechnikov, retrieved on November 28, 2008. From Nobel Lectures, Physiology or Medicine 1901–1921, Elsevier Publishing Company, Amsterdam, 1967.
- Janeway, Charles A. 2001. Evolution of the innate immune system. In Janeway, Charles; Paul Travers, Mark Walport, and Mark Shlomchik. Immunobiology, p598. 5th ed, New York and London: Garland Science. ISBN 978-0-8153-4101-7
- Ernst J.D. & Stendahl O. (eds) 2006. Phagocytosis of bacteria and bacterial pathogenicity. New York: Cambridge University Press, p. 10, 186. ISBN 0-521-84569-6
- Robinson J.P. & Babcock G.F. (eds) 1998. Phagocyte function – a guide for research and clinical evaluation. New York: Wiley–Liss, p. 187. ISBN 0-471-12364-1
- Thompson C.B. (1995). "Apoptosis in the pathogenesis and treatment of disease". Science 267 (5203): 1456–62. . .
- Janeway, Charles; Paul Travers, Mark Walport, and Mark Shlomchik 2001. Immunobiology. 5th ed. New York and London: Garland Science. ISBN 978-0-8153-4101-7 Chapter: Induced innate responses to infection.
- Fang FC (October 2004). "Antimicrobial reactive oxygen and nitrogen species: concepts and controversies". Nat. Rev. Microbiol. 2 (10): 820–32. . .
- Janeway, Charles; Paul Travers, Mark Walport, and Mark Shlomchik 2001. Immunobiology. 5th ed. New York and London: Garland Science. ISBN 978-0-8153-4101-7 Chapter: Antigen presentation to T lymphocytes.
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